**The Positive and Negative Aspects of Reactive Oxygen Species in Sports Performance**

Guolin Li

[73] Sureira TM, Amancio OS, Braga JAP. Influence of Artistic Gymnastics on Iron Nutri‐ tional Status and Exercise-Induced Hemolysis in Female Athletes. International Jour‐

[74] Telford RD, Sly GJ, Hahn AG, Cunningham RB, Bryant C, Smith JA. Footstrike is the major cause of hemolysis during running. Journal of Applied Physiology 2003; 94(1):

[75] Selby GB, Eichner ER. Endurance Swimming, Intravascular Hemolysis, Anemia, and Iron Depletion - New Perspective on Athletes Anemia. American Journal of Medicine

[76] Hallberg L, Hogdahl, A, Nilsson L, Rybo G. Menstrual blood loss - A Population

[77] Larsson G, Milsom I, Lindstedt G, Rybo G. The Influence of a Low-Dose Combined Oral-Contraceptive on Menstrual Blood-Loss and Iron Status. Contraception 1992;

[78] Schoene RB, Escourrou P, Robertson HT, Nilson KL, Parsons JR, Smith NJ. Iron Re‐ pletion Decreases Maximal Exercise Lactate Concentrations in Female Athletes with Minimal Iron-Deficiency Anemia. Journal of Laboratory and Clinical Medicine 1983;

[79] Pitsis GC, Fallon KE, Fallon SK, Fazakerley R. Response of soluble transferrin recep‐ tor and iron-related parameters to iron supplementation in elite, iron-depleted, nona‐

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study Acta obst. et gynec. scandinav 1966; 45: 320-351.

38-42.

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168 Current Issues in Sports and Exercise Medicine

46(4): 327-334.

102(2): 306-312.

Additional information is available at the end of the chapter

http://dx.doi.org/10.5772/53360

## **1. Introduction**

Physical exercise, especially moderate physical exercise, can benefit health in a wide range of ways [1-3]. Evidence from different age groups, genders and races has revealed that regular physical exercise is associated with high levels of physical fitness and a reduced risk of mortality, while sedentary habits are related to low levels of physical fitness and an increased threat of all-cause mortality [1-8]. However, the physiological mechanism of physical exerciseinduced physical fitness remains only partly understood.

During physical exercise, the metabolic rate increases greatly, as quantified by oxygen consumption and heat production, which results in an enhanced generation of reactive oxygen species (ROS). ROS describe both oxygen-centred free radicals and reactive non-radical derivatives of oxygen resulting from a sequential reduction of oxygen through the addition of electrons. Table 1 shows the representative ROS. The role of ROS in physical exercise is frequently misunderstood. Most people tend to either overemphasize the deleterious role of ROS by maintaining that any ROS generation in vivo during exercise would damage cellular constituents, or underemphasize the beneficial effect of exercise-induced ROS by assuming that the body has enough ROS in vivo that it needs. Two breakthroughs, the identification of ROS in redox regulation and findings on the role of antioxidant supplementation in preventing health-promoting effects of physical exercise, have led scientists to re-examine the role of ROS, especially their positive influence. The goal of this chapter is to outline the current evidence on the sites of ROS generation during exercise, the role of exercise-induced ROS, the effects of antioxidant supplementation on physical-exercise-induced physical fitness, and the mecha‐ nism of ROS in exercise-induced adaptation.

© 2013 Li; licensee InTech. This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. © 2013 Li; licensee InTech. This is a paper distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


such as the analysis of thiobarbituric acid reactive substances (TBARS) or end products of lipid peroxidation [47, 48]. As indicated by these indirect methods, a significant number of studies suggest an increase of ROS during exercise, especially during bouts of intensive exercise [47-49]. Some studies have found that, in comparison to sedentary control, the muscular malondialdehyde (MDA) levels of muscle homogenates in rats exposed to periods of exhaus‐ tive exercise increased by more than 100% [47]. The administration of vitamin E can reduce the damage to skeletal muscle [50-52], and muscles from vitamin-E-deficient mice or rats are more likely to be damaged during contractile activity [47, 53]. Based on these early studies, some researchers have suggested that mitochondria are the predominant site for generating ROS during exercise [47], and that the generating rate is related to mitochondrial oxygen

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Confusingly, some studies have found little or no change in muscular TBARS or MDA levels after exercise. The results from Alessio et al. have demonstrated that the levels of TBARS do not increase significantly with exhaustive aerobic or nonaerobic isometric exercise [56]. Other studies also show that moderate-intensity resistance exercise had no effects on serum MDA concentration in both resistance-trained and untrained subjects [57], and graded exercise to fatigue did not promote an increase in MDA levels [58]. Though the exact reason is still unclear, the methodical variation between studies, the nonspecific nature of TBARS assay [59, 60], the reactivity of MDA and other aldehydes [61], or even the rapid clearance of TBARS from plasma

Still, it cannot be concluded that exercise does not alter the levels of ROS even if the TBARS or MDA levels do not change. In fact, there is much evidence for oxidative stress after exhaustive exercise, although the levels of TBARS do not increase [56]. Therefore, if the direct evidence that indicates increasing ROS levels during exercise is lacking, it is difficult to conclude that

The emergence of new technologies, especially electron spin resonance/electron paramagnetic resonance (ESR or EPR) spectroscopy, has made the direct detection of free radicals *in vivo* possible. To our knowledge, though EPR/ESR is not sensitive to the concentrations of free radicals typically found in biological systems, it is the only direct method to assay free radicals. In 1982, Davies and collaborators provided the first direct proof that high-intensity exercise enhances free radical production as indicated by a heightened ESR signal (around g=2.004) in muscle and liver homogenates [47]. Other studies have provided further evidence to suggest that exercise promotes ROS generation. Intriguingly, the increase of ROS seems to play some roles in muscle damage caused by extensive muscular activity, as 30 minutes of excessive contractile activity of rat hind-limb muscles shows an average 70% increase in the amplitude of the major ESR signal, and also a leakage of intracellular creatine kinase enzyme into the

These observations have prompted researchers to look for more details on the kinds of ROS that are formed in muscles during or after exercise. Based on ESR/EPR signals, Davies and collaborators have found that the concentration of two ubisemiquinone free radicals (presum‐ ably Qi and Qo) is very high in exercised animals [64]. A result from extracellular fluid by

the damage incurred during contractile activity is mediated by ROS.

consumption [54, 55].

[62], may account for this issue.

blood plasma [63].

**Table 1.** Name (Radical depiction) of reactive oxygen species (ROS)

## **2. Evidence of ros generation in exercise**

Exercise has been shown to alter oxidative stress in a wide range of body fluids, cells and/or tissues in human beings, rodents and other animals. These include commonly used model tissues, such as blood [9-11] and skeletal muscle [9, 12-14], along with many other models less often used for laboratory research, such as neutrophils [15-17], lymphocytes [18-20], the diaphragm [21, 22], liver [23-25], heart [23, 26-28], lung [22, 29], brain [30-32], kidney [33, 34], spleen [35, 36], and thymus [35, 37, 38], as well as urine [39-41] and exhaled breath [42, 43].

Although oxidative stress is a common response of cells or tissues to exercise, this does not suggest that all models respond in a similar way to the same exercise. In fact, the levels of ROS generation are different across tissues and/or cells even at rest, let alone during exercise. There is some good evidence that the basal rate of superoxide anion production within the liver of the sperm whale is the highest, more than fourfold higher than that in the brain, about threefold higher than in the heart and muscle, and twofold higher than in the kidney [44]. Another indirect piece of evidence indicates that the heart contains about a tenfold higher level of lipid peroxide than the liver in rats [45]. Moreover, different forms of exercise result in different levels of oxidative stress depending on organ or tissue types. The responses to oxidative stress in the heart and muscle caused by eight-week treadmill running (chronic exercise) or treadmill running to exhaustion (acute exercise) are quite different from those in the brain and liver of rats [46]. This is possibly due to the differences in mitochondrial biogenesis and the occurrence of oxidant-induced degeneration.

The following sections therefore present the evidence on ROS generation during exercise in different tissues or organs.

#### **2.1. Muscle**

To explore the relationships between oxidative stress and sports medicine, the majority of researchers have focused on muscles for the reason that their contractions are primarily responsible for all force production and movement, as well as maintenance of and changes in posture.

ROS are hard to be detected because they are highly unstable and short-lived. In early studies, due to the limitations in the analytical techniques and approaches available to detect ROS directly, the levels of ROS are commonly evaluated through indirect and nonspecific methods, such as the analysis of thiobarbituric acid reactive substances (TBARS) or end products of lipid peroxidation [47, 48]. As indicated by these indirect methods, a significant number of studies suggest an increase of ROS during exercise, especially during bouts of intensive exercise [47-49]. Some studies have found that, in comparison to sedentary control, the muscular malondialdehyde (MDA) levels of muscle homogenates in rats exposed to periods of exhaus‐ tive exercise increased by more than 100% [47]. The administration of vitamin E can reduce the damage to skeletal muscle [50-52], and muscles from vitamin-E-deficient mice or rats are more likely to be damaged during contractile activity [47, 53]. Based on these early studies, some researchers have suggested that mitochondria are the predominant site for generating ROS during exercise [47], and that the generating rate is related to mitochondrial oxygen consumption [54, 55].

**Oxygen-centred free radicals Reactive non-radical derivatives of oxygen**

hydrogen peroxide (H2O2) singlet oxygen (1Δg)

ozone (O3)

Exercise has been shown to alter oxidative stress in a wide range of body fluids, cells and/or tissues in human beings, rodents and other animals. These include commonly used model tissues, such as blood [9-11] and skeletal muscle [9, 12-14], along with many other models less often used for laboratory research, such as neutrophils [15-17], lymphocytes [18-20], the diaphragm [21, 22], liver [23-25], heart [23, 26-28], lung [22, 29], brain [30-32], kidney [33, 34], spleen [35, 36], and thymus [35, 37, 38], as well as urine [39-41] and exhaled breath [42, 43]. Although oxidative stress is a common response of cells or tissues to exercise, this does not suggest that all models respond in a similar way to the same exercise. In fact, the levels of ROS generation are different across tissues and/or cells even at rest, let alone during exercise. There is some good evidence that the basal rate of superoxide anion production within the liver of the sperm whale is the highest, more than fourfold higher than that in the brain, about threefold higher than in the heart and muscle, and twofold higher than in the kidney [44]. Another indirect piece of evidence indicates that the heart contains about a tenfold higher level of lipid peroxide than the liver in rats [45]. Moreover, different forms of exercise result in different levels of oxidative stress depending on organ or tissue types. The responses to oxidative stress in the heart and muscle caused by eight-week treadmill running (chronic exercise) or treadmill running to exhaustion (acute exercise) are quite different from those in the brain and liver of rats [46]. This is possibly due to the differences in mitochondrial biogenesis and the occurrence

The following sections therefore present the evidence on ROS generation during exercise in

To explore the relationships between oxidative stress and sports medicine, the majority of researchers have focused on muscles for the reason that their contractions are primarily responsible for all force production and movement, as well as maintenance of and changes in

ROS are hard to be detected because they are highly unstable and short-lived. In early studies, due to the limitations in the analytical techniques and approaches available to detect ROS directly, the levels of ROS are commonly evaluated through indirect and nonspecific methods,

superoxide anion (O2˙ˉ ) hydroxyl radical (HO˙) peroxyl radical (RO2˙) alkoxyl radical (RO˙)

170 Current Issues in Sports and Exercise Medicine

**Table 1.** Name (Radical depiction) of reactive oxygen species (ROS)

**2. Evidence of ros generation in exercise**

of oxidant-induced degeneration.

different tissues or organs.

**2.1. Muscle**

posture.

Confusingly, some studies have found little or no change in muscular TBARS or MDA levels after exercise. The results from Alessio et al. have demonstrated that the levels of TBARS do not increase significantly with exhaustive aerobic or nonaerobic isometric exercise [56]. Other studies also show that moderate-intensity resistance exercise had no effects on serum MDA concentration in both resistance-trained and untrained subjects [57], and graded exercise to fatigue did not promote an increase in MDA levels [58]. Though the exact reason is still unclear, the methodical variation between studies, the nonspecific nature of TBARS assay [59, 60], the reactivity of MDA and other aldehydes [61], or even the rapid clearance of TBARS from plasma [62], may account for this issue.

Still, it cannot be concluded that exercise does not alter the levels of ROS even if the TBARS or MDA levels do not change. In fact, there is much evidence for oxidative stress after exhaustive exercise, although the levels of TBARS do not increase [56]. Therefore, if the direct evidence that indicates increasing ROS levels during exercise is lacking, it is difficult to conclude that the damage incurred during contractile activity is mediated by ROS.

The emergence of new technologies, especially electron spin resonance/electron paramagnetic resonance (ESR or EPR) spectroscopy, has made the direct detection of free radicals *in vivo* possible. To our knowledge, though EPR/ESR is not sensitive to the concentrations of free radicals typically found in biological systems, it is the only direct method to assay free radicals. In 1982, Davies and collaborators provided the first direct proof that high-intensity exercise enhances free radical production as indicated by a heightened ESR signal (around g=2.004) in muscle and liver homogenates [47]. Other studies have provided further evidence to suggest that exercise promotes ROS generation. Intriguingly, the increase of ROS seems to play some roles in muscle damage caused by extensive muscular activity, as 30 minutes of excessive contractile activity of rat hind-limb muscles shows an average 70% increase in the amplitude of the major ESR signal, and also a leakage of intracellular creatine kinase enzyme into the blood plasma [63].

These observations have prompted researchers to look for more details on the kinds of ROS that are formed in muscles during or after exercise. Based on ESR/EPR signals, Davies and collaborators have found that the concentration of two ubisemiquinone free radicals (presum‐ ably Qi and Qo) is very high in exercised animals [64]. A result from extracellular fluid by microdialysis has also shown that a 15-min protocol of 180 isometric contractions can induce a rapid increase in superoxide anion concentrations and hydroxyl radical activity [65].

tive acute exercise, indiscriminately induces oxidative stress in the liver, while endurance or

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173

Important to note is that the liver is distinct from muscles that directly participate in contractile activity or produce forces to support movement. It is logical to consider that the impact of exercise on hepatic oxidative stress should not be the same as the impact on muscles. Results from acute sprint exercise in mice have confirmed this concept. Although the exercise causes an increase in TBARS levels in skeletal muscle, there is no change in the liver [81]. Furthermore, exercise training appears to have little effect on hepatic or myocardial enzyme systems, but can cause adaptive effects in skeletal muscle antioxidant enzymes [82]. A study to investigate the responses to oxidative stress induced by chronic or acute exercise in the brain, liver, heart, kidney, and muscles of rats has also shown that the responses from the brain and liver to oxidative stress are quite different from those in the heart and muscles, and the difference may

long-term training shows a beneficial role in ameliorating oxidative stress.

be attributed to the organ or tissue types and endogenous antioxidant levels [46].

**2.3. Brain**

the key issues.

researchers in recent years.

Although the potential mechanism for generating ROS induced by exercise in muscles has been explored in depth, the related mechanism in the liver has not been extensively studied. Based on the above evidence, the mechanism for ROS production in the liver should be greatly different from that in muscles. Further research is needed to reveal the detailed mechanisms, and the energy stress and hepatic ischemia reperfusion should be given particular attention.

Exercise has been reported to benefit the brain or nervous system in a wide range of ways, while oxidative stress is involved in the pathogenesis of several age-related nervous diseases. Therefore, the links between exercise-induced alteration of ROS generation in the brain and the potential beneficial effects of exercise on the brain have attracted great attention from

Intense physical training can significantly increase TBARS levels and decrease the levels of the brain-derived neurotrophic factors (BDNF) in the brain cortex of mice, which promotes brain mitochondrial dysfunction [83]. Acute and exhaustive swimming exercise has also been reported to elevate the lipid peroxidation and ROS formation in the brain tissue of rats [84, 85], while long-term dietary restriction or selenium supplementation protects against the oxidative stress [84, 85]. Vitamin E deficiency may promote mitochondrial H2O2 generation, lipid peroxidation and protein oxidation in the brain [86]. However, vitamin C supplementa‐ tion has been shown to offer no protection against exercise-induced oxidative damage in brain tissue [87]. Swimming does not significantly influence the oxidative damage, nor is it reflected in the carbonyl content [88], and even over-training does not significantly change the levels of TBARS, 8-hydroxydeoxyguanosine or other biomarkers of oxidative stress in rat brains significantly [89]. Aerobic exercise does not affect lipid peroxidation of the brain, but a diabetic condition improves the activities of several antioxidant enzymes [90]. Though different brain regions of rats react differentially in response to acute exercise-induced oxidative stress, as reported by Somani *et al.* [91, 92], and this may explain some of the discrepancies, differences in the type of exercise, the analytic technique and the age, sex and strain of animals should be

Based on the well-characterized *in vitro* models of single isolated muscles or cultured myo‐ tubes, researchers have identified a series of ROS and provided evidence that muscles are under considerable oxidative stress after contractile activities, especially lengthening contrac‐ tile activities. Reid and colleagues have shown that muscular contraction increases intracellular levels of superoxide anion radicals and hydrogen peroxide (H2O2), and these ROS promote low-frequency fatigue [66]. Subsequent data from the same group also identify superoxide anion in the extracellular space of diaphragm muscle fibres, and the level is enhanced by fatiguing muscular contractions [67]. When the cultured myotubes are stimulated to contract with different frequencies of electrical stimulation, there is a release of superoxide anion and nitric oxide (NO) into the extracellular medium and an increase in extracellular hydroxyl radical activity [68]. Through loading fluorescein probes with single intact muscle fibres, other studies have developed a method to measure the intracellular ROS generation *in situ* by realtime fluorescence microscopy and illustrated a net increase of ROS by contractions of isolated fibres [69]. It is now possible to analyse different ROS by using different fluorescein probes. The intracellular NO production is visualized in real time using the fluorescent NO probe 4 amino-5-methylamino-2',7'-difluorofluorescein diacetate [70]. With the use of 2',7'-dichloro‐ dihydrofluorescein as an intracellular probe, researchers have confirmed the dynamic changes of ROS levels during contractile activity in skeletal muscle myotubes [71]. The rate of ROS generation does not change significantly over 30 min in resting myotubes, but it is increased approximately fourfold during 10 min of repetitive contractile activities [71], and the super‐ oxide scavenger Tiron can effectively negate the rise in intracellular fluorescence [71]. Recently, several other probes have also been developed, which permit the monitoring of different ROS in specific cells or organelles [69-74], and will provide more detailed evidence for the exerciseinduced increase of ROS. Of note is that, since there are limitations to the most widely used fluorescent probes for detecting and measuring ROS, researchers should be cautious with regard to the optimal use of selected fluorescent probes and interpretation of results [75].

Despite the challenges of detection and the inconsistent results from different methods or models, significant studies have provided evidence for exhaustive exercise promoting extensive ROS formation in muscles (for reviews, see [76-78]).

## **2.2. Liver**

A great deal of research has detected an alteration of ROS in the liver during or after exercise. When Davies *et al*. provided the first direct evidence for ROS generation in muscles after exhaustive exercise, they also found a rise of free radicals in liver homogenates [47]. TBARS, an indicator of lipid peroxidation, has also been reported to increase in the liver and muscles subsequent to exercise, and dietary vitamin E supplementation can reduce (but not eliminate) the increase of TBARS in the liver [79]. Endurance training shows a decreased level of MDA and protein carbonylation, and a significant increase in the activity of superoxide dismutase in mice [80]. Consistent with the effects of exercise on oxidative stress in muscles, most of the other available studies have also suggested that acute exercise, especially intensive or exhaus‐ tive acute exercise, indiscriminately induces oxidative stress in the liver, while endurance or long-term training shows a beneficial role in ameliorating oxidative stress.

Important to note is that the liver is distinct from muscles that directly participate in contractile activity or produce forces to support movement. It is logical to consider that the impact of exercise on hepatic oxidative stress should not be the same as the impact on muscles. Results from acute sprint exercise in mice have confirmed this concept. Although the exercise causes an increase in TBARS levels in skeletal muscle, there is no change in the liver [81]. Furthermore, exercise training appears to have little effect on hepatic or myocardial enzyme systems, but can cause adaptive effects in skeletal muscle antioxidant enzymes [82]. A study to investigate the responses to oxidative stress induced by chronic or acute exercise in the brain, liver, heart, kidney, and muscles of rats has also shown that the responses from the brain and liver to oxidative stress are quite different from those in the heart and muscles, and the difference may be attributed to the organ or tissue types and endogenous antioxidant levels [46].

Although the potential mechanism for generating ROS induced by exercise in muscles has been explored in depth, the related mechanism in the liver has not been extensively studied. Based on the above evidence, the mechanism for ROS production in the liver should be greatly different from that in muscles. Further research is needed to reveal the detailed mechanisms, and the energy stress and hepatic ischemia reperfusion should be given particular attention.

#### **2.3. Brain**

microdialysis has also shown that a 15-min protocol of 180 isometric contractions can induce a rapid increase in superoxide anion concentrations and hydroxyl radical activity [65].

172 Current Issues in Sports and Exercise Medicine

Based on the well-characterized *in vitro* models of single isolated muscles or cultured myo‐ tubes, researchers have identified a series of ROS and provided evidence that muscles are under considerable oxidative stress after contractile activities, especially lengthening contrac‐ tile activities. Reid and colleagues have shown that muscular contraction increases intracellular levels of superoxide anion radicals and hydrogen peroxide (H2O2), and these ROS promote low-frequency fatigue [66]. Subsequent data from the same group also identify superoxide anion in the extracellular space of diaphragm muscle fibres, and the level is enhanced by fatiguing muscular contractions [67]. When the cultured myotubes are stimulated to contract with different frequencies of electrical stimulation, there is a release of superoxide anion and nitric oxide (NO) into the extracellular medium and an increase in extracellular hydroxyl radical activity [68]. Through loading fluorescein probes with single intact muscle fibres, other studies have developed a method to measure the intracellular ROS generation *in situ* by realtime fluorescence microscopy and illustrated a net increase of ROS by contractions of isolated fibres [69]. It is now possible to analyse different ROS by using different fluorescein probes. The intracellular NO production is visualized in real time using the fluorescent NO probe 4 amino-5-methylamino-2',7'-difluorofluorescein diacetate [70]. With the use of 2',7'-dichloro‐ dihydrofluorescein as an intracellular probe, researchers have confirmed the dynamic changes of ROS levels during contractile activity in skeletal muscle myotubes [71]. The rate of ROS generation does not change significantly over 30 min in resting myotubes, but it is increased approximately fourfold during 10 min of repetitive contractile activities [71], and the super‐ oxide scavenger Tiron can effectively negate the rise in intracellular fluorescence [71]. Recently, several other probes have also been developed, which permit the monitoring of different ROS in specific cells or organelles [69-74], and will provide more detailed evidence for the exerciseinduced increase of ROS. Of note is that, since there are limitations to the most widely used fluorescent probes for detecting and measuring ROS, researchers should be cautious with regard to the optimal use of selected fluorescent probes and interpretation of results [75].

Despite the challenges of detection and the inconsistent results from different methods or models, significant studies have provided evidence for exhaustive exercise promoting

A great deal of research has detected an alteration of ROS in the liver during or after exercise. When Davies *et al*. provided the first direct evidence for ROS generation in muscles after exhaustive exercise, they also found a rise of free radicals in liver homogenates [47]. TBARS, an indicator of lipid peroxidation, has also been reported to increase in the liver and muscles subsequent to exercise, and dietary vitamin E supplementation can reduce (but not eliminate) the increase of TBARS in the liver [79]. Endurance training shows a decreased level of MDA and protein carbonylation, and a significant increase in the activity of superoxide dismutase in mice [80]. Consistent with the effects of exercise on oxidative stress in muscles, most of the other available studies have also suggested that acute exercise, especially intensive or exhaus‐

extensive ROS formation in muscles (for reviews, see [76-78]).

**2.2. Liver**

Exercise has been reported to benefit the brain or nervous system in a wide range of ways, while oxidative stress is involved in the pathogenesis of several age-related nervous diseases. Therefore, the links between exercise-induced alteration of ROS generation in the brain and the potential beneficial effects of exercise on the brain have attracted great attention from researchers in recent years.

Intense physical training can significantly increase TBARS levels and decrease the levels of the brain-derived neurotrophic factors (BDNF) in the brain cortex of mice, which promotes brain mitochondrial dysfunction [83]. Acute and exhaustive swimming exercise has also been reported to elevate the lipid peroxidation and ROS formation in the brain tissue of rats [84, 85], while long-term dietary restriction or selenium supplementation protects against the oxidative stress [84, 85]. Vitamin E deficiency may promote mitochondrial H2O2 generation, lipid peroxidation and protein oxidation in the brain [86]. However, vitamin C supplementa‐ tion has been shown to offer no protection against exercise-induced oxidative damage in brain tissue [87]. Swimming does not significantly influence the oxidative damage, nor is it reflected in the carbonyl content [88], and even over-training does not significantly change the levels of TBARS, 8-hydroxydeoxyguanosine or other biomarkers of oxidative stress in rat brains significantly [89]. Aerobic exercise does not affect lipid peroxidation of the brain, but a diabetic condition improves the activities of several antioxidant enzymes [90]. Though different brain regions of rats react differentially in response to acute exercise-induced oxidative stress, as reported by Somani *et al.* [91, 92], and this may explain some of the discrepancies, differences in the type of exercise, the analytic technique and the age, sex and strain of animals should be the key issues.

Under conditions of aging or stress, or pathological conditions, the oxidative stress in the brain increases rapidly. Exercise may improve these conditions through strengthening the function of antioxidant defence systems and/or decreasing oxidative stress. Habitual exercise has been reported to overcome the age-related deficit in antioxidant enzymes and prevent oxidative damage in aged brain [93, 94]. There is considerable evidence for physical exercise playing an important preventive and therapeutic role in oxidative stress-associated diseases, such as in reducing oxidative stress after traumatic brain injury [32], increasing thioredoxin-1 levels [95] and the activities of antioxidant enzymes [90] in diabetic brains, and restoring the antioxidant system in the brain of hyperphenylalaninemic rats [96]. Furthermore, exercise-induced modulation of the redox state is an important means to withstand oxidative stress under stress conditions. It has been suggested that exercise may promote mitochondrial function, expres‐ sions of mitofusin and antioxidant enzymes against chronic unpredictable mild stress in the brain [97], and reverse the decrease in BDNF and the increase in ROS induced by consuming a high-fat diet [98].

white blood cells, exercise results in substantial improvements in markers of DNA and RNA

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The impacts of gender on exercise-induced oxidative stress should not be ignored. Females seem to be more protected against oxidative stress induced by swimming. H2O2 is mainly produced in males, which subsequently leads to the increase of MnSOD gene expression and

Mitochondria have often been cited as the major site of ROS generation in tissues. Based on the classic works by Chance and his collaborators, when mitochondria are in state 4, about 2% of total oxygen consumed by mitochondria is converted into H2O2 and other ROS [99, 100]. As oxygen consumption increases greatly during exercise, many researchers have assumed that mitochondria should be a key site of ROS formation, and the extent of ROS generation may be related to the oxygen consumption by mitochondria [54, 55]. When Davies and colleagues found the first direct evidence for exercise-induced ROS formation, they also suggested mitochondria as the predominant source [47]. This hypothesis seems to be confirmed by subsequent data. Davies and Hochstein did identify two free radicals, that is, two forms of semistabilized mitochondrial ubisemiquinone (presumably Qi and Qo) [64]. They found that the concentration of the two free radicals was obviously higher in exercised animals than in control animals, which has actually provided the first evidence for the mitochondrial genera‐ tion of free radicals induced by exercise *in vivo* [64]. Other EPR signal studies also supported

*In vitro* experiments have indicated that mitochondrial ROS generation is lower in state 3 than in state 4 respiration [100]. There is considerable evidence that muscular mitochondria are predominant in state 3 rather than in state 4 during aerobic contractile activity, which would limit the ROS formation during contractions [102, 103]. This has led other researchers to support the above hypothesis of mitochondria as a main site of ROS generation. To explore the specific site of exercise associated with ROS production, Puente-Maestu *et al.* isolated mitochondria from skeletal muscle of chronic obstructive pulmonary disease (COPD) patients at rest and after exercise, and analysed mitochondrial oxygen consumption and ROS produc‐ tion [49]. Then, they related the *in vitro* ROS production during the state 3 respiration with skeletal muscle oxidative stress after exercise [49]. They found that mitochondrial complex III was the main site of producing H2O2 in mitochondria of skeletal muscle, and the mitochondrial production of H2O2 in the state 3 respiration contributed to exercise-induced muscle oxidative

Another argument regards the semiquinone radicals. McArdle and his colleagues assayed the effects of repeated lengthening contractions on semiquinone-derived free radical signal, oxidation of protein thiols and glutathione, and lipid peroxidation in the extensor digitorum

damage [39].

activity [20].

damage [49].

**3. Sites of ROS generation in exercise**

the importance of mitochondria in ROS production [63, 101].

**3.1. ROS generation by mitochondria**

In summary, the effect of exercise on the brain is complex. Although the current data on exercise-induced redox alternation in the brain is still conflicted, there is overwhelming evidence that habitual and regular exercise is an important way to improve brain function by enhancing resistance against oxidative stress and facilitating recovery from oxidative stress. Further investigation is needed to identify the biological basis for the association of exercise, ROS and brain functions.

## **2.4. Others**

Muscular contractile activity has been proven to promote the generation of ROS, and the redox status in the brain and liver may also be altered after physical exercise. However, the effect of exercise on the oxidative stress of other tissues or cells is not consistent. This discrepancy in the findings may be attributed to the differences in exercise type, duration and intensity across protocols, as well as the differences in cells and/or tissues.

Oxidative damage occurs in lymphoid tissues after exhaustive exercise [35], and vigorous exercise has also been reported to result in a transient increase of oxidative stress in lympho‐ cytes [18]. For cigarette smokers, maximal exercise induces pulmonary oxidative stress and leads to oxidative damage in the lungs [42], while in normal lungs exercise neither leads to significant oxidative stress, nor alters mitochondrial respiration [22]. For trained men, even strenuous bouts of exercise do not cause a significant increase in blood oxidative stress, which may be related to the attenuation in ROS production as an adaptation to chronic exercise training [11].

Intriguingly, in rat kidneys exercise training has been noted to prevent oxidative stress and inflammation and to preserve antioxidant status, which mediates the effects of chronic exercise on preserving renal haemodynamics and structure [33, 34]. In rat hearts, prolonged exercise could upregulate the mRNA expression and activity of uncoupling protein 2 (UCP2], which may reduce cross-membrane potential and thus ROS production [27]. However, endurance training can blunt exercise-induced UCP2 activation, and increase removal of ROS [27]. In white blood cells, exercise results in substantial improvements in markers of DNA and RNA damage [39].

The impacts of gender on exercise-induced oxidative stress should not be ignored. Females seem to be more protected against oxidative stress induced by swimming. H2O2 is mainly produced in males, which subsequently leads to the increase of MnSOD gene expression and activity [20].

## **3. Sites of ROS generation in exercise**

## **3.1. ROS generation by mitochondria**

Under conditions of aging or stress, or pathological conditions, the oxidative stress in the brain increases rapidly. Exercise may improve these conditions through strengthening the function of antioxidant defence systems and/or decreasing oxidative stress. Habitual exercise has been reported to overcome the age-related deficit in antioxidant enzymes and prevent oxidative damage in aged brain [93, 94]. There is considerable evidence for physical exercise playing an important preventive and therapeutic role in oxidative stress-associated diseases, such as in reducing oxidative stress after traumatic brain injury [32], increasing thioredoxin-1 levels [95] and the activities of antioxidant enzymes [90] in diabetic brains, and restoring the antioxidant system in the brain of hyperphenylalaninemic rats [96]. Furthermore, exercise-induced modulation of the redox state is an important means to withstand oxidative stress under stress conditions. It has been suggested that exercise may promote mitochondrial function, expres‐ sions of mitofusin and antioxidant enzymes against chronic unpredictable mild stress in the brain [97], and reverse the decrease in BDNF and the increase in ROS induced by consuming

In summary, the effect of exercise on the brain is complex. Although the current data on exercise-induced redox alternation in the brain is still conflicted, there is overwhelming evidence that habitual and regular exercise is an important way to improve brain function by enhancing resistance against oxidative stress and facilitating recovery from oxidative stress. Further investigation is needed to identify the biological basis for the association of exercise,

Muscular contractile activity has been proven to promote the generation of ROS, and the redox status in the brain and liver may also be altered after physical exercise. However, the effect of exercise on the oxidative stress of other tissues or cells is not consistent. This discrepancy in the findings may be attributed to the differences in exercise type, duration and intensity across

Oxidative damage occurs in lymphoid tissues after exhaustive exercise [35], and vigorous exercise has also been reported to result in a transient increase of oxidative stress in lympho‐ cytes [18]. For cigarette smokers, maximal exercise induces pulmonary oxidative stress and leads to oxidative damage in the lungs [42], while in normal lungs exercise neither leads to significant oxidative stress, nor alters mitochondrial respiration [22]. For trained men, even strenuous bouts of exercise do not cause a significant increase in blood oxidative stress, which may be related to the attenuation in ROS production as an adaptation to chronic exercise

Intriguingly, in rat kidneys exercise training has been noted to prevent oxidative stress and inflammation and to preserve antioxidant status, which mediates the effects of chronic exercise on preserving renal haemodynamics and structure [33, 34]. In rat hearts, prolonged exercise could upregulate the mRNA expression and activity of uncoupling protein 2 (UCP2], which may reduce cross-membrane potential and thus ROS production [27]. However, endurance training can blunt exercise-induced UCP2 activation, and increase removal of ROS [27]. In

protocols, as well as the differences in cells and/or tissues.

a high-fat diet [98].

174 Current Issues in Sports and Exercise Medicine

ROS and brain functions.

**2.4. Others**

training [11].

Mitochondria have often been cited as the major site of ROS generation in tissues. Based on the classic works by Chance and his collaborators, when mitochondria are in state 4, about 2% of total oxygen consumed by mitochondria is converted into H2O2 and other ROS [99, 100]. As oxygen consumption increases greatly during exercise, many researchers have assumed that mitochondria should be a key site of ROS formation, and the extent of ROS generation may be related to the oxygen consumption by mitochondria [54, 55]. When Davies and colleagues found the first direct evidence for exercise-induced ROS formation, they also suggested mitochondria as the predominant source [47]. This hypothesis seems to be confirmed by subsequent data. Davies and Hochstein did identify two free radicals, that is, two forms of semistabilized mitochondrial ubisemiquinone (presumably Qi and Qo) [64]. They found that the concentration of the two free radicals was obviously higher in exercised animals than in control animals, which has actually provided the first evidence for the mitochondrial genera‐ tion of free radicals induced by exercise *in vivo* [64]. Other EPR signal studies also supported the importance of mitochondria in ROS production [63, 101].

*In vitro* experiments have indicated that mitochondrial ROS generation is lower in state 3 than in state 4 respiration [100]. There is considerable evidence that muscular mitochondria are predominant in state 3 rather than in state 4 during aerobic contractile activity, which would limit the ROS formation during contractions [102, 103]. This has led other researchers to support the above hypothesis of mitochondria as a main site of ROS generation. To explore the specific site of exercise associated with ROS production, Puente-Maestu *et al.* isolated mitochondria from skeletal muscle of chronic obstructive pulmonary disease (COPD) patients at rest and after exercise, and analysed mitochondrial oxygen consumption and ROS produc‐ tion [49]. Then, they related the *in vitro* ROS production during the state 3 respiration with skeletal muscle oxidative stress after exercise [49]. They found that mitochondrial complex III was the main site of producing H2O2 in mitochondria of skeletal muscle, and the mitochondrial production of H2O2 in the state 3 respiration contributed to exercise-induced muscle oxidative damage [49].

Another argument regards the semiquinone radicals. McArdle and his colleagues assayed the effects of repeated lengthening contractions on semiquinone-derived free radical signal, oxidation of protein thiols and glutathione, and lipid peroxidation in the extensor digitorum longus muscles of rats. Although they found the oxidation of protein thiols and glutathione was enhanced after contractions, the magnitude of the semiquinone-derived free radical signal observed by ESR was the same in exercised and non-exercised skeletal muscles [104]. To further explore the site of ROS generation during exercise, another study [65] isolated the gastrocne‐ mius muscles from MnSOD knockout heterozygous (Sod2+/-) and wild-type (Sod2+/+) mice, and measured the concentrations of superoxide anions and hydroxyl radical activity in the extracellular space by microdialysis. They found that isometric contractions induced a rapid, equivalent increase in superoxide anion concentrations in the extracellular space of both Sod2+/- and Sod2+/+ mice, whereas hydroxyl radical activity increased only in the extracellular space of muscles of Sod2+/+ mice [65]. In other words, a reduction in MnSOD activity did not change the concentration of superoxide anions in the extracellular space, but decreased the concentration of hydroxyl radicals in the extracellular space. Considering that MnSOD is located in the mitochondrial matrix, these results suggest that mitochondria are the key sites in converting superoxide anions to hydroxyl radicals. Furthermore, mice with skeletal-musclespecific deficiency of MnSOD (muscle-Sod2-/-) also demonstrated a severe disturbance in exercise activity, increased oxidative damage and reduced ATP content in their muscle tissue, while a single administration of the antioxidant EUK-8 significantly improved the exercise activity and ATP level [14]. These findings indicate that even if the mitochondrion is not the major site, it is at least an important site in generating superoxide anions in muscles during exercise.

CuZnSOD activities, reduce oxidative stress and improve skeletal muscle function in response to electrically stimulated isometric contractions [108]. In most cases in other animals, evidence has also been provided for the beneficial effects of allopurinol or oxypurinol in inhibiting XO and thus attenuating the generation of ROS. Lipid hydroperoxides, GSSG and the formation of ROS during exercise are reduced significantly in an allopurinol-treated horse [109]. Exercise could cause an increase in blood XO activity in rats, and inhibiting XO with allopurinol could prevent exercise-induced oxidation of glutathione in both rats and human beings [110]. Furthermore, allopurinol has also been shown to decrease oxidative stress and ameliorate the morbidity and mortality of congestive heart failure patients (for reviews, see [111]). In the light of these observations, some researchers have suggested that XO may play a more important

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However, results from Capecchi *et al.* have shown that allopurinol has no effect on superoxide anion generation or enzyme release from neutrophils stimulated *in vitro* with formyl-me‐ thionyl-leucyl-phenylalanine [113]. Nor do more recent observations support the critical role of XO in generating ROS during intensive exercise. Olek and colleagues tested the effects of allopurinol ingestion on the slow component of VO2 kinetics (the dynamic behaviour of O2 uptake in the transition from rest to exercise) and the alternations of plasma oxidative stress markers during severe intensity exercise. They found short-term intensive exercise could induce oxidative stress, and although allopurinol intake might cause an increase in resting xanthine and hypoxanthine plasma concentrations (supporting XO inhibition by allopurinol), it neither modified the kinetics of oxygen consumption nor altered ROS overproduction [114].

Gomez-Cabrera *et al.* [115] examined the effects of allopurinol on the inhibition of ROS production and on the activation of nuclear factor kappaB (NFκB) in rats subjected to exhaus‐ tive exercise. They found that exercise did result in considerably more glutathione oxidation in the control rat than in the rat administered with allopurinol before exercise. However, the administration of allopurinol could also negate the exercise-induced activation of NFκB, which is an important signalling pathway involved in upregulating the expression of important enzymes for cell defence (superoxide dismutase) and adaptation to exercise. That is to say, at the same time as allopurinol decreases XO-mediated oxidative stress, it also prevents useful

Except for mitochondria and XO, there should be other sites of ROS production during and after exercise. When tissue damage has occurred, several cells in the immune system (including macrophages/monocytes, eosinohpils and neutrophils) may also generate large quantities of ROS [116]. For example, circulating neutrophils has been reported to produce ROS due to the facilitation of myeloperoxidase degranulation after exhaustive exercise [17]. Although more investigation is needed to fully elucidate the mechanism and site of ROS formation in exercise,

at the present time mitochondria and XO are still worth focusing on.

role in generating ROS than mitochondria do [112].

cellular adaptations to exercise in rats.

**3.3. Other sites and current understanding**

In light of the above observations, the electron transport associated with the mitochondrial respiratory chain is considered the central process leading to ROS production during exercise.

#### **3.2. ROS generation by xanthine oxidase**

Another possible site for ROS generation during exercise, especially intensive or exhaustive exercise, is xanthine oxidase (XO). As an intensive or exhaustive exercise can result in ische‐ mia or hypoxia in certain regions of the body, massive ATP depletion occurs and ATP will be converted to adenosine diphosphate, adenosine monophosphate, inosine, and finally hypoxan‐ thine. Under normal physiological conditions, xanthine dehydrogenase is the dominant form of XO, which can catalyse the oxidation of hypoxanthine to xanthine or further the oxidation of xanthine to uric acid by using NAD+ as an electron acceptor. However, under ischemia conditions, the xanthine dehydrogenase can be converted to XO by reversible sulfhydryl oxidation or by irreversible proteolytic modification [105, 106], and XO can no longer utilize NAD+ as the electron acceptor, instead using molecular oxygen as the electron acceptor and yielding four units of superoxide anions per unit of transformed substrate. As a result, under reperfusion conditions, a burst of superoxide anions and H2O2 can result [107].

XO has been thought to be responsible for the production of ROS and tissue damage during or after intensive exercise, and the inhibition of XO by allopurinol or oxypurinol can reduce the production of ROS. Ryan and collaborators measured XO activity, H2O2 levels, lipid peroxidation, the activities of antioxidant enzymes, and skeletal muscle function in aged mice with or without administration of allopurinol. In addition to finding inhibition of XO by allopurinol treatment, they found the treatment could prevent the increase of catalase and CuZnSOD activities, reduce oxidative stress and improve skeletal muscle function in response to electrically stimulated isometric contractions [108]. In most cases in other animals, evidence has also been provided for the beneficial effects of allopurinol or oxypurinol in inhibiting XO and thus attenuating the generation of ROS. Lipid hydroperoxides, GSSG and the formation of ROS during exercise are reduced significantly in an allopurinol-treated horse [109]. Exercise could cause an increase in blood XO activity in rats, and inhibiting XO with allopurinol could prevent exercise-induced oxidation of glutathione in both rats and human beings [110]. Furthermore, allopurinol has also been shown to decrease oxidative stress and ameliorate the morbidity and mortality of congestive heart failure patients (for reviews, see [111]). In the light of these observations, some researchers have suggested that XO may play a more important role in generating ROS than mitochondria do [112].

However, results from Capecchi *et al.* have shown that allopurinol has no effect on superoxide anion generation or enzyme release from neutrophils stimulated *in vitro* with formyl-me‐ thionyl-leucyl-phenylalanine [113]. Nor do more recent observations support the critical role of XO in generating ROS during intensive exercise. Olek and colleagues tested the effects of allopurinol ingestion on the slow component of VO2 kinetics (the dynamic behaviour of O2 uptake in the transition from rest to exercise) and the alternations of plasma oxidative stress markers during severe intensity exercise. They found short-term intensive exercise could induce oxidative stress, and although allopurinol intake might cause an increase in resting xanthine and hypoxanthine plasma concentrations (supporting XO inhibition by allopurinol), it neither modified the kinetics of oxygen consumption nor altered ROS overproduction [114].

Gomez-Cabrera *et al.* [115] examined the effects of allopurinol on the inhibition of ROS production and on the activation of nuclear factor kappaB (NFκB) in rats subjected to exhaus‐ tive exercise. They found that exercise did result in considerably more glutathione oxidation in the control rat than in the rat administered with allopurinol before exercise. However, the administration of allopurinol could also negate the exercise-induced activation of NFκB, which is an important signalling pathway involved in upregulating the expression of important enzymes for cell defence (superoxide dismutase) and adaptation to exercise. That is to say, at the same time as allopurinol decreases XO-mediated oxidative stress, it also prevents useful cellular adaptations to exercise in rats.

## **3.3. Other sites and current understanding**

longus muscles of rats. Although they found the oxidation of protein thiols and glutathione was enhanced after contractions, the magnitude of the semiquinone-derived free radical signal observed by ESR was the same in exercised and non-exercised skeletal muscles [104]. To further explore the site of ROS generation during exercise, another study [65] isolated the gastrocne‐ mius muscles from MnSOD knockout heterozygous (Sod2+/-) and wild-type (Sod2+/+) mice, and measured the concentrations of superoxide anions and hydroxyl radical activity in the extracellular space by microdialysis. They found that isometric contractions induced a rapid, equivalent increase in superoxide anion concentrations in the extracellular space of both Sod2+/- and Sod2+/+ mice, whereas hydroxyl radical activity increased only in the extracellular space of muscles of Sod2+/+ mice [65]. In other words, a reduction in MnSOD activity did not change the concentration of superoxide anions in the extracellular space, but decreased the concentration of hydroxyl radicals in the extracellular space. Considering that MnSOD is located in the mitochondrial matrix, these results suggest that mitochondria are the key sites in converting superoxide anions to hydroxyl radicals. Furthermore, mice with skeletal-musclespecific deficiency of MnSOD (muscle-Sod2-/-) also demonstrated a severe disturbance in exercise activity, increased oxidative damage and reduced ATP content in their muscle tissue, while a single administration of the antioxidant EUK-8 significantly improved the exercise activity and ATP level [14]. These findings indicate that even if the mitochondrion is not the major site, it is at least an important site in generating superoxide anions in muscles during

In light of the above observations, the electron transport associated with the mitochondrial respiratory chain is considered the central process leading to ROS production during exercise.

Another possible site for ROS generation during exercise, especially intensive or exhaustive exercise, is xanthine oxidase (XO). As an intensive or exhaustive exercise can result in ische‐ mia or hypoxia in certain regions of the body, massive ATP depletion occurs and ATP will be converted to adenosine diphosphate, adenosine monophosphate, inosine, and finally hypoxan‐ thine. Under normal physiological conditions, xanthine dehydrogenase is the dominant form of XO, which can catalyse the oxidation of hypoxanthine to xanthine or further the oxidation of xanthine to uric acid by using NAD+ as an electron acceptor. However, under ischemia conditions, the xanthine dehydrogenase can be converted to XO by reversible sulfhydryl oxidation or by irreversible proteolytic modification [105, 106], and XO can no longer utilize

 as the electron acceptor, instead using molecular oxygen as the electron acceptor and yielding four units of superoxide anions per unit of transformed substrate. As a result, under

XO has been thought to be responsible for the production of ROS and tissue damage during or after intensive exercise, and the inhibition of XO by allopurinol or oxypurinol can reduce the production of ROS. Ryan and collaborators measured XO activity, H2O2 levels, lipid peroxidation, the activities of antioxidant enzymes, and skeletal muscle function in aged mice with or without administration of allopurinol. In addition to finding inhibition of XO by allopurinol treatment, they found the treatment could prevent the increase of catalase and

reperfusion conditions, a burst of superoxide anions and H2O2 can result [107].

exercise.

NAD+

**3.2. ROS generation by xanthine oxidase**

176 Current Issues in Sports and Exercise Medicine

Except for mitochondria and XO, there should be other sites of ROS production during and after exercise. When tissue damage has occurred, several cells in the immune system (including macrophages/monocytes, eosinohpils and neutrophils) may also generate large quantities of ROS [116]. For example, circulating neutrophils has been reported to produce ROS due to the facilitation of myeloperoxidase degranulation after exhaustive exercise [17]. Although more investigation is needed to fully elucidate the mechanism and site of ROS formation in exercise, at the present time mitochondria and XO are still worth focusing on.

## **4. Role of ROS in exercise: Foe or friend?**

Sedentary habits are associated with low levels of cardiorespiratory fitness and an increased threat of all-cause mortality, while physically active habits are associated with fitness im‐ provement and reduced mortality risk [1, 7, 117]. However, the detailed mechanism of physical activity-induced physical fitness remains only partly understood.

participating in regular and adequate training would enhance antioxidant capacity and bring about improvement in both peripheral resistance to insulin and all the functional metabolic interchanges in cellular membranes [125]. Intriguingly, leisure time, moderate occupational or household physical activities are also positively related to total antioxidant capacity, and

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In particular conditions, however, although exercise prevents some pathologic processes, it increases oxidative stress. As illustrated in elderly people, sustained exercise enhances cardiorespiratory function and reduces the risk of cardiovascular disease, but it also signifi‐ cantly enhances some biomarkers of oxidative stress [127]. This is also the case in atherogenic mice. Exercise lowered plasma cholesterol and atherosclerotic lesions, with a concomitant increase in oxidative stress and endothelial NO synthase [128]. In this condition, though vitamin E supplementation can decrease the exercise-induced oxidative stress, it also coun‐ teracts the beneficial effects of exercise on atherosclerosis and hinders the induction of arterial antioxidant response [128]. These findings have led to researchers beginning to consider the

Early studies in this area have focused on the oxidative damage induced by augmented formation of ROS. Subsequent data, however, have shown that ROS also participate in redox regulation, and it has been widely accepted that the moderate concentrations of ROS *in vivo* function as regulatory mediators in signalling processes and as initiators in re-establishing ''redox homeostasis" [129, 130]. There are now a significant number of studies suggesting that regular exercise can enhance the capacity of antioxidant defence systems to lower oxidative stress or the levels of ROS. In this context, some researchers have begun to speculate a positive role of a transient high level of ROS induced by exercise. This hypothesis has been confirmed in a rat diaphragm. In this study, fibre bundles from a rat diaphragm were incubated with exogenous catalase or SOD to decrease the tissue level of ROS, and then the peak twitch stress, time-to-peak tension and half-relaxation time were measured. The results showed that either selective removal of H2O2 with catalase or selective removal of superoxide anions with SOD depressed submaximal contractile activities in a dose-dependent way [131]. These findings indicate the ROS present in non-fatigued muscle can promote excitation-contraction coupling and are responsible for optimal contractile function [131]. Subsequently, many studies have documented a role of ROS as second messengers responsible for the prevention of diseases by stimulating antioxidant response [128], or other adaptations to exercise by activating useful cellular redox signalling pathways including peroxisome proliferator-activated receptorgamma coactivator-1alpha [132], mitogen-activated protein kinase and NFκB [115, 133].

Moreover, it is now clear that ROS not only play an important role in regulating muscle contractile activity, but are also involved in promoting muscle regeneration in recovery from muscle damage [134], improving insulin sensitivity [135], and mediating the vasodilatory response during exercise [136]. As a result, ROS generated in response to exercise and other physiological or pathological stimuli might be important signalling molecules rather than

can decrease the risk of cardiovascular disease [126].

positive effects of ROS themselves.

*4.2.2. Beneficial role of ROS in exercise*

solely by-products of energy metabolism.

Since 1982, when Davies *et al.* provided the first direct proof that high-intensity exercise enhances free radical production [47], further evidence has emerged for exercise promoting ROS formation. Besides mitochondria, XO and phagocytes in skeletal muscle have also been reported to be potentially responsible for generating ROS in response to exercise [77]. Here, it is necessary to substantiate the role of ROS in sports medicine and in exercise-induced effects.

## **4.1. Harmful effect of ROS in exercise**

ROS form as a natural by-product of normal energy metabolism. They have been considered as toxic molecules due to their high reactivity to most of the biological macromolecules, which generally include DNA damage, oxidations of polyunsaturated fatty acids and amino acids, and oxidative inactivation of specific enzymes.

As aerobic exercise will undoubtedly increase the metabolic rate in the body, the harmful effects of exercise and exercise-induced ROS are well documented. Exercise localized to a peripheral muscle group in COPD patients has been shown to induce systemic oxidative stress [118]. Acute exercise-induced oxidative stress contributes to post-exercise proteinuria in untrained rats [119]. A maximal bicycle exercise results in DNA strand breaks and oxidative DNA damage [120]. High-competition swimming imposes high and sustained oxidative and proteolytic stress on adolescents, which may increase potential risk of cardiovascular disease in the future [121]. A run-to-exhaustion exercise leads to an increase in oxidative damage of lymphoid tissues in rats [122].

In summary, strenuous exercise under conditions of disease or overtraining would signifi‐ cantly elevate respiration rate, lead to a dramatic and sustained increase in ROS that is more than the antioxidant defence system can scavenge, and eventually result in oxidative stress and damage to physiological functions. Therefore, though regular exercise is important to improve cardiorespiratory fitness, extreme or exhaustive physical activities should be avoided, especially under certain disease conditions.

## **4.2. Beneficial role of ROS in exercise**

## *4.2.1. Oxidative stress and beneficial effect of exercise*

There is growing evidence for the healthy role of exercise. Some studies indicate its beneficial effect is associated with the attenuation of oxidative stress. It is reported that regular training can ameliorate ethanol-induced oxidative injury in the liver [123], endurance training may attenuate exercise-induced oxidative stress [25], and chronic exercise can improve antioxidant status and induce a reduction in arterial hypertension development in rats [124]. Athletes participating in regular and adequate training would enhance antioxidant capacity and bring about improvement in both peripheral resistance to insulin and all the functional metabolic interchanges in cellular membranes [125]. Intriguingly, leisure time, moderate occupational or household physical activities are also positively related to total antioxidant capacity, and can decrease the risk of cardiovascular disease [126].

In particular conditions, however, although exercise prevents some pathologic processes, it increases oxidative stress. As illustrated in elderly people, sustained exercise enhances cardiorespiratory function and reduces the risk of cardiovascular disease, but it also signifi‐ cantly enhances some biomarkers of oxidative stress [127]. This is also the case in atherogenic mice. Exercise lowered plasma cholesterol and atherosclerotic lesions, with a concomitant increase in oxidative stress and endothelial NO synthase [128]. In this condition, though vitamin E supplementation can decrease the exercise-induced oxidative stress, it also coun‐ teracts the beneficial effects of exercise on atherosclerosis and hinders the induction of arterial antioxidant response [128]. These findings have led to researchers beginning to consider the positive effects of ROS themselves.

## *4.2.2. Beneficial role of ROS in exercise*

**4. Role of ROS in exercise: Foe or friend?**

178 Current Issues in Sports and Exercise Medicine

**4.1. Harmful effect of ROS in exercise**

lymphoid tissues in rats [122].

especially under certain disease conditions.

*4.2.1. Oxidative stress and beneficial effect of exercise*

**4.2. Beneficial role of ROS in exercise**

and oxidative inactivation of specific enzymes.

activity-induced physical fitness remains only partly understood.

Sedentary habits are associated with low levels of cardiorespiratory fitness and an increased threat of all-cause mortality, while physically active habits are associated with fitness im‐ provement and reduced mortality risk [1, 7, 117]. However, the detailed mechanism of physical

Since 1982, when Davies *et al.* provided the first direct proof that high-intensity exercise enhances free radical production [47], further evidence has emerged for exercise promoting ROS formation. Besides mitochondria, XO and phagocytes in skeletal muscle have also been reported to be potentially responsible for generating ROS in response to exercise [77]. Here, it is necessary to substantiate the role of ROS in sports medicine and in exercise-induced effects.

ROS form as a natural by-product of normal energy metabolism. They have been considered as toxic molecules due to their high reactivity to most of the biological macromolecules, which generally include DNA damage, oxidations of polyunsaturated fatty acids and amino acids,

As aerobic exercise will undoubtedly increase the metabolic rate in the body, the harmful effects of exercise and exercise-induced ROS are well documented. Exercise localized to a peripheral muscle group in COPD patients has been shown to induce systemic oxidative stress [118]. Acute exercise-induced oxidative stress contributes to post-exercise proteinuria in untrained rats [119]. A maximal bicycle exercise results in DNA strand breaks and oxidative DNA damage [120]. High-competition swimming imposes high and sustained oxidative and proteolytic stress on adolescents, which may increase potential risk of cardiovascular disease in the future [121]. A run-to-exhaustion exercise leads to an increase in oxidative damage of

In summary, strenuous exercise under conditions of disease or overtraining would signifi‐ cantly elevate respiration rate, lead to a dramatic and sustained increase in ROS that is more than the antioxidant defence system can scavenge, and eventually result in oxidative stress and damage to physiological functions. Therefore, though regular exercise is important to improve cardiorespiratory fitness, extreme or exhaustive physical activities should be avoided,

There is growing evidence for the healthy role of exercise. Some studies indicate its beneficial effect is associated with the attenuation of oxidative stress. It is reported that regular training can ameliorate ethanol-induced oxidative injury in the liver [123], endurance training may attenuate exercise-induced oxidative stress [25], and chronic exercise can improve antioxidant status and induce a reduction in arterial hypertension development in rats [124]. Athletes

Early studies in this area have focused on the oxidative damage induced by augmented formation of ROS. Subsequent data, however, have shown that ROS also participate in redox regulation, and it has been widely accepted that the moderate concentrations of ROS *in vivo* function as regulatory mediators in signalling processes and as initiators in re-establishing ''redox homeostasis" [129, 130]. There are now a significant number of studies suggesting that regular exercise can enhance the capacity of antioxidant defence systems to lower oxidative stress or the levels of ROS. In this context, some researchers have begun to speculate a positive role of a transient high level of ROS induced by exercise. This hypothesis has been confirmed in a rat diaphragm. In this study, fibre bundles from a rat diaphragm were incubated with exogenous catalase or SOD to decrease the tissue level of ROS, and then the peak twitch stress, time-to-peak tension and half-relaxation time were measured. The results showed that either selective removal of H2O2 with catalase or selective removal of superoxide anions with SOD depressed submaximal contractile activities in a dose-dependent way [131]. These findings indicate the ROS present in non-fatigued muscle can promote excitation-contraction coupling and are responsible for optimal contractile function [131]. Subsequently, many studies have documented a role of ROS as second messengers responsible for the prevention of diseases by stimulating antioxidant response [128], or other adaptations to exercise by activating useful cellular redox signalling pathways including peroxisome proliferator-activated receptorgamma coactivator-1alpha [132], mitogen-activated protein kinase and NFκB [115, 133].

Moreover, it is now clear that ROS not only play an important role in regulating muscle contractile activity, but are also involved in promoting muscle regeneration in recovery from muscle damage [134], improving insulin sensitivity [135], and mediating the vasodilatory response during exercise [136]. As a result, ROS generated in response to exercise and other physiological or pathological stimuli might be important signalling molecules rather than solely by-products of energy metabolism.

#### **4.3. Current understanding**

Thanks to evidence gathered over the last three decades, we now understand the effects of exercise and the role of exercise-induced ROS more clearly. During exercise, although oxygen consumption in the body increases more than tenfold, the intracellular H2O2 concentrations in skeletal muscle induced by contractile activities only increase by approximately 100 nM [78]. This modest increase of H2O2 can only be enough to assume the functions of the signalling molecule and to stimulate some of the adaptations of muscle to exercise. ROS are not only toxic but also involved in cell signalling and in regulating several redox-sensitive transcription factors [115, 132, 133]. An inhibition of ROS generation would also modify cellular redox signalling pathways associated with adaptations to exercise [115, 132, 133]. It is now clear that physical activities cause oxidative stress only when exhaustive. ROS induced by moderate exercise may serve as signalling molecules to increase the expression of cytoprotective proteins and to maintain some other normal functions. Habitual and regular exercise is a useful strategy for improving physical fitness and reducing mortality risk.

muscles in aged rodents [140]. Although the most widely studied antioxidants are vitamin E and ascorbic acid (vitamin C), the effects on suppressing exercise-induced oxidative stress have also demonstrated in other antioxidants, including β-carotene [141], N-acetylcysteine (NAC) [142], L-arginine [143], coenzyme Q [144], α-lipoic acid [145], resveratrol [146], several other compounds [147, 148], selenium [149], teas [150], and concentrates from fruit, berry and

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However, many studies show that the administration of antioxidants, alone or in combination, does not significantly affect exercise-induced oxidative stress [134, 152-157]. Several observa‐ tions even indicate an increase of oxidative stress following antioxidant supplementation preor post-exercise, especially with high doses [158-162]. Moreover, some investigations that have confirmed the beneficial effects of antioxidants on oxidative stress did not demonstrate a significant improvement in performance [163] or the functions related to pain and muscle damage [151]. Therefore, the health-promoting effects of antioxidants should be explored in

The role of antioxidant supplementation in protecting against fatigue remains highly contro‐ versial. One reason for this controversy is the lack of strong evidence for oxidative stress involved in muscle fatigue. Some studies have displayed an association between oxidative stress and muscle fatigue [164, 165], and the anabolic androgenic steroid stanozolol, a drug used in sport to enhance muscle mass and strength and to increase muscle fatigue resistance, can protect against acute exercise-induced oxidative stress by reducing mitochondrial ROS production [13]. However, the association has been challenged by other observations that suggest that graded exercise to fatigue does not promote an increase in oxidative stress in the blood of exercise-trained heart transplant recipients [58], and an enhanced running time to exhaustion does not lead to attenuation of lipid peroxidation [166]. As a result, although NAC supplementation has been reported to improve muscle fatigue in rats [167], it does not affect the time to fatigue in a group of untrained men [168], or in those participating in submaximal

The processes of force production during repetitive eccentric exercise have been widely accepted to result in muscle damage, which is specifically the case when the exercise is unaccustomed. Given that high levels of ROS generated during contractile activities may contribute to the muscle damage (for reviews, see [170, 171]), and antioxidants may scavenge ROS, the potential preventive effects of antioxidant supplementation on muscle damage have been explored in depth, with variations in dosage, timing and duration of administration. Most of the research has focused on the effects of vitamin C and E. Some studies do find some protecting role of the two antioxidants against oxidative stress, while there is no strong evidence for their role in preventing muscle damage (for reviews, see[172]). However, some findings do not support a major role for antioxidant supplementation to reduce markers of oxidative stress [134, 152, 173, 174]. There appears to be no independent or combined effect of

vegetable [151].

more detail.

cycling exercises [169].

**5.2. Antioxidant supplementation and fatigue**

**5.3. Antioxidant supplementation and muscle damage**

## **5. Antioxidant supplementation in exercise: Beneficial or detrimental?**

ROS are unavoidable by-products of energy metabolism, and cells continuously generate ROS in metabolic processes. High metabolic rates during exercise have led to the assumption that exercise leads to excessive production of ROS in skeletal muscle, which is associated with muscle damage and impaired muscle function. As a result, the supplementation of antioxi‐ dants may offer some protection against exercise-induced oxidative damage, and improve muscle function and physical performance. In this context, numerous antioxidants are marketed, and antioxidant supplementation has become very common with athletes or other physically active individuals. However, there is not enough scientific evidence to support their efficacy and long-term safety.

#### **5.1. Antioxidant supplementation and oxidative stress**

The majority of studies have illustrated that antioxidants attenuate the oxidative stress induced by exercise, although oxidative stress is estimated through measuring its indirect outcomes, such as by-products of lipid peroxidation, protein oxidation and DNA damage. A study by Alessio *et al.* tested the effects of vitamin C supplementation for one day and two weeks on oxidative stress in subjects with or without exercise. When the subjects were at rest, they found that vitamin C supplementations did not affect the levels of TBARS or oxygen radical absorb‐ ance capacity, but with the same subjects after 30 minutes of exercise, the supplementation did prevent the increase of oxidative stress [137]. Oral ingestion of vitamin C has been reported to effectively prevent exercise-induced lipid peroxidation in patients with type 1 diabetes mellitus [138]. The supplementation of vitamin E can diminish the increase of lipid hydroper‐ oxides and TBARS in the plasma and muscle fibres of rats following aerobic exercise [139]. The combined administration of vitamin E and C improves indices of oxidative stress associated with repetitive loading exercise and aging, and ameliorates the positive work output of muscles in aged rodents [140]. Although the most widely studied antioxidants are vitamin E and ascorbic acid (vitamin C), the effects on suppressing exercise-induced oxidative stress have also demonstrated in other antioxidants, including β-carotene [141], N-acetylcysteine (NAC) [142], L-arginine [143], coenzyme Q [144], α-lipoic acid [145], resveratrol [146], several other compounds [147, 148], selenium [149], teas [150], and concentrates from fruit, berry and vegetable [151].

However, many studies show that the administration of antioxidants, alone or in combination, does not significantly affect exercise-induced oxidative stress [134, 152-157]. Several observa‐ tions even indicate an increase of oxidative stress following antioxidant supplementation preor post-exercise, especially with high doses [158-162]. Moreover, some investigations that have confirmed the beneficial effects of antioxidants on oxidative stress did not demonstrate a significant improvement in performance [163] or the functions related to pain and muscle damage [151]. Therefore, the health-promoting effects of antioxidants should be explored in more detail.

## **5.2. Antioxidant supplementation and fatigue**

**4.3. Current understanding**

180 Current Issues in Sports and Exercise Medicine

efficacy and long-term safety.

for improving physical fitness and reducing mortality risk.

**5.1. Antioxidant supplementation and oxidative stress**

Thanks to evidence gathered over the last three decades, we now understand the effects of exercise and the role of exercise-induced ROS more clearly. During exercise, although oxygen consumption in the body increases more than tenfold, the intracellular H2O2 concentrations in skeletal muscle induced by contractile activities only increase by approximately 100 nM [78]. This modest increase of H2O2 can only be enough to assume the functions of the signalling molecule and to stimulate some of the adaptations of muscle to exercise. ROS are not only toxic but also involved in cell signalling and in regulating several redox-sensitive transcription factors [115, 132, 133]. An inhibition of ROS generation would also modify cellular redox signalling pathways associated with adaptations to exercise [115, 132, 133]. It is now clear that physical activities cause oxidative stress only when exhaustive. ROS induced by moderate exercise may serve as signalling molecules to increase the expression of cytoprotective proteins and to maintain some other normal functions. Habitual and regular exercise is a useful strategy

**5. Antioxidant supplementation in exercise: Beneficial or detrimental?**

ROS are unavoidable by-products of energy metabolism, and cells continuously generate ROS in metabolic processes. High metabolic rates during exercise have led to the assumption that exercise leads to excessive production of ROS in skeletal muscle, which is associated with muscle damage and impaired muscle function. As a result, the supplementation of antioxi‐ dants may offer some protection against exercise-induced oxidative damage, and improve muscle function and physical performance. In this context, numerous antioxidants are marketed, and antioxidant supplementation has become very common with athletes or other physically active individuals. However, there is not enough scientific evidence to support their

The majority of studies have illustrated that antioxidants attenuate the oxidative stress induced by exercise, although oxidative stress is estimated through measuring its indirect outcomes, such as by-products of lipid peroxidation, protein oxidation and DNA damage. A study by Alessio *et al.* tested the effects of vitamin C supplementation for one day and two weeks on oxidative stress in subjects with or without exercise. When the subjects were at rest, they found that vitamin C supplementations did not affect the levels of TBARS or oxygen radical absorb‐ ance capacity, but with the same subjects after 30 minutes of exercise, the supplementation did prevent the increase of oxidative stress [137]. Oral ingestion of vitamin C has been reported to effectively prevent exercise-induced lipid peroxidation in patients with type 1 diabetes mellitus [138]. The supplementation of vitamin E can diminish the increase of lipid hydroper‐ oxides and TBARS in the plasma and muscle fibres of rats following aerobic exercise [139]. The combined administration of vitamin E and C improves indices of oxidative stress associated with repetitive loading exercise and aging, and ameliorates the positive work output of

The role of antioxidant supplementation in protecting against fatigue remains highly contro‐ versial. One reason for this controversy is the lack of strong evidence for oxidative stress involved in muscle fatigue. Some studies have displayed an association between oxidative stress and muscle fatigue [164, 165], and the anabolic androgenic steroid stanozolol, a drug used in sport to enhance muscle mass and strength and to increase muscle fatigue resistance, can protect against acute exercise-induced oxidative stress by reducing mitochondrial ROS production [13]. However, the association has been challenged by other observations that suggest that graded exercise to fatigue does not promote an increase in oxidative stress in the blood of exercise-trained heart transplant recipients [58], and an enhanced running time to exhaustion does not lead to attenuation of lipid peroxidation [166]. As a result, although NAC supplementation has been reported to improve muscle fatigue in rats [167], it does not affect the time to fatigue in a group of untrained men [168], or in those participating in submaximal cycling exercises [169].

#### **5.3. Antioxidant supplementation and muscle damage**

The processes of force production during repetitive eccentric exercise have been widely accepted to result in muscle damage, which is specifically the case when the exercise is unaccustomed. Given that high levels of ROS generated during contractile activities may contribute to the muscle damage (for reviews, see [170, 171]), and antioxidants may scavenge ROS, the potential preventive effects of antioxidant supplementation on muscle damage have been explored in depth, with variations in dosage, timing and duration of administration. Most of the research has focused on the effects of vitamin C and E. Some studies do find some protecting role of the two antioxidants against oxidative stress, while there is no strong evidence for their role in preventing muscle damage (for reviews, see[172]). However, some findings do not support a major role for antioxidant supplementation to reduce markers of oxidative stress [134, 152, 173, 174]. There appears to be no independent or combined effect of vitamin C, vitamin E and other antioxidants supplementation on facilitating recovery of muscle function after exercise-induced muscle damage [152], protecting against the delayed onset of muscle soreness and markers of muscle damage [173], or attenuating muscular damage induced by exhaustive exercise such as a marathon run [174]. On the contrary, a number of investigations suggest that the administration of antioxidants may promote cellular damage [161], transiently increase tissue damage [162], and hinder the recovery of muscle damage [134]. Therefore, recent studies have cast doubt on the benign effects of antioxidant supplementation.

buffering capacity enhancement is a physiological mechanism to explain exercise-induced physical fitness [130]. This hypothesis seems to be a good framework to illustrate the role of

The Positive and Negative Aspects of Reactive Oxygen Species in Sports Performance

http://dx.doi.org/10.5772/53360

183

Hormesis is basically characterized by biphasic dose-response –low-dose stimulation and high-dose inhibition [175-177]. This is often used to refer to the beneficial effects of low doses of potentially harmful substances [175-177]. As described in section 2, exercise is associated with the increased generation of ROS. This may be the reason for early studies considering aerobic exercise as a mild oxidative stressor [139, 178]. Indeed, sustained high doses of ROS are unquestionably deleterious, whereas a large amount of evidence emerging in recent years has suggested that a mild increase of ROS may evoke a cellular adaptive response to exercise.

More than two decades ago, Sterling and Eyer coined the term allostasis from the Greek "allo" meaning "variable", and "stasis" meaning "stable". Thus, allostasis means "remaining stable by being variable" [179], that is, maintaining stability through a multi-point. Since in organ‐ isms, especially in higher animals, the stability of the internal milieu is associated with many rhythms, such as daily rhythm of body temperature, daily rhythmic secretion of serotonin, melatonin and other hormones, and many other rhythms, allostasis should be a more accurate concept than homeostasis (remaining stable by staying the same). Although there is no evidence at present to show that redox *in vivo* remains stable by being variable, numerous studies have suggested that the increased formation of ROS, whether induced by aging, exercise, or other stress conditions, is initiated to re-establish "redox homeostasis" (for review, see [129]). From a rigorous scientific point of view, the term "redox homeostasis" used here

Based on the multi-point property of allostasis, we have postulated the allostatic system as a special "buffering system": it has a basal level and certain buffering capacity that can maintain dynamic stability. Therefore, we have coined the term "allostatic buffering capacity (ABC)" with five components: basal level, peak level, buffering range, increase rate and recovery rate, to give a good picture of the capacity of an allostatic system to maintain dynamic stability. The action model of exercise on ABC has also been addressed. For more details, readers are

Regular exercise can promote mitochondrial biogenesis and enhance muscle oxidative capacity [180, 181], and the molecular signals are mainly the increased ROS, such as H2O2 [180, 181]. In addition, exercise training has been reported to decrease ROS production through

Therefore, ROS-induced response has the typical bi-phasic features of hormesis.

**6.2. ROS-induced enhancement of allostatic buffering capacity**

ROS in exercise-induced physical fitness.

*6.2.1. ROS and allostatic buffering capacity*

should be replaced by "redox allostasis".

recommended to read our review published in 2009 [130].

*6.2.2. Present evidence of exercise-induced ROS to enhance redox ABC*

**6.1. Exercise, ROS and hormesis**

## **5.4. Antioxidant supplementation and exercise performance**

Similar to equivocal effects of antioxidant administration on muscle damage, present results regarding the role of antioxidant supplementation in exercise performance are inconsistent. There is some evidence to display that the supplementation of antioxidant can benefit exercise performance, while the majority of studies do not support it. Even the combined supplemen‐ tation of vitamins E, C, NAC, coenzyme Q10, polyprenols and other antioxidants in different subject populations and exercise protocols fails to improve exercise performance. Moreover, there is increasing evidence suggesting a deleterious effect of antioxidant supplementation on exercise performance. For more details on this issue, readers are recommended to read an excellent recently published review by Peternelj and Coombes [136].

#### **5.5. Current understanding**

ROS formation during exercise may have dual effects. High levels of ROS produced during strenuous exercise may be related to oxidative damage and impaired muscle function. However, the moderate or transient high levels of ROS induced by exercise may act as signalling molecules to stimulate adaptive responses through redox-sensitive signalling pathways to maintain cellular redox homeostasis during exercise. This scenario explains why subjects involved in exercise training have shown an increase of resistance to oxidative stress under a wide range of physiological and pathological stresses.

Although the majority of studies on the supplementation of antioxidants have supported their beneficial effects on attenuating exercise-induced oxidative stress, there is limited evidence for antioxidant treatment offering any protection against exercise-induced muscular function damage or exercise performance. A plausible explanation is that the attenuation of ROS by antioxidant supplementation may block some useful cell signalling pathways and gene expression involved in adaptations to exercise, which may preclude the health-promoting effects of exercise in subjects.

## **6. The mechanism of ROS for exercise-induced physical fitness**

Despite great progress made in sports medicine, the mechanism of exercise-induced physical fitness remains only partly understood. Combined with the hormetic characteristic of physical activity and the property of allostasis, we have assumed that hormesis-induced allostatic buffering capacity enhancement is a physiological mechanism to explain exercise-induced physical fitness [130]. This hypothesis seems to be a good framework to illustrate the role of ROS in exercise-induced physical fitness.

## **6.1. Exercise, ROS and hormesis**

vitamin C, vitamin E and other antioxidants supplementation on facilitating recovery of muscle function after exercise-induced muscle damage [152], protecting against the delayed onset of muscle soreness and markers of muscle damage [173], or attenuating muscular damage induced by exhaustive exercise such as a marathon run [174]. On the contrary, a number of investigations suggest that the administration of antioxidants may promote cellular damage [161], transiently increase tissue damage [162], and hinder the recovery of muscle damage [134]. Therefore, recent studies have cast doubt on the benign effects of antioxidant

Similar to equivocal effects of antioxidant administration on muscle damage, present results regarding the role of antioxidant supplementation in exercise performance are inconsistent. There is some evidence to display that the supplementation of antioxidant can benefit exercise performance, while the majority of studies do not support it. Even the combined supplemen‐ tation of vitamins E, C, NAC, coenzyme Q10, polyprenols and other antioxidants in different subject populations and exercise protocols fails to improve exercise performance. Moreover, there is increasing evidence suggesting a deleterious effect of antioxidant supplementation on exercise performance. For more details on this issue, readers are recommended to read an

ROS formation during exercise may have dual effects. High levels of ROS produced during strenuous exercise may be related to oxidative damage and impaired muscle function. However, the moderate or transient high levels of ROS induced by exercise may act as signalling molecules to stimulate adaptive responses through redox-sensitive signalling pathways to maintain cellular redox homeostasis during exercise. This scenario explains why subjects involved in exercise training have shown an increase of resistance to oxidative stress

Although the majority of studies on the supplementation of antioxidants have supported their beneficial effects on attenuating exercise-induced oxidative stress, there is limited evidence for antioxidant treatment offering any protection against exercise-induced muscular function damage or exercise performance. A plausible explanation is that the attenuation of ROS by antioxidant supplementation may block some useful cell signalling pathways and gene expression involved in adaptations to exercise, which may preclude the health-promoting

Despite great progress made in sports medicine, the mechanism of exercise-induced physical fitness remains only partly understood. Combined with the hormetic characteristic of physical activity and the property of allostasis, we have assumed that hormesis-induced allostatic

**6. The mechanism of ROS for exercise-induced physical fitness**

**5.4. Antioxidant supplementation and exercise performance**

excellent recently published review by Peternelj and Coombes [136].

under a wide range of physiological and pathological stresses.

supplementation.

182 Current Issues in Sports and Exercise Medicine

**5.5. Current understanding**

effects of exercise in subjects.

Hormesis is basically characterized by biphasic dose-response –low-dose stimulation and high-dose inhibition [175-177]. This is often used to refer to the beneficial effects of low doses of potentially harmful substances [175-177]. As described in section 2, exercise is associated with the increased generation of ROS. This may be the reason for early studies considering aerobic exercise as a mild oxidative stressor [139, 178]. Indeed, sustained high doses of ROS are unquestionably deleterious, whereas a large amount of evidence emerging in recent years has suggested that a mild increase of ROS may evoke a cellular adaptive response to exercise. Therefore, ROS-induced response has the typical bi-phasic features of hormesis.

## **6.2. ROS-induced enhancement of allostatic buffering capacity**

## *6.2.1. ROS and allostatic buffering capacity*

More than two decades ago, Sterling and Eyer coined the term allostasis from the Greek "allo" meaning "variable", and "stasis" meaning "stable". Thus, allostasis means "remaining stable by being variable" [179], that is, maintaining stability through a multi-point. Since in organ‐ isms, especially in higher animals, the stability of the internal milieu is associated with many rhythms, such as daily rhythm of body temperature, daily rhythmic secretion of serotonin, melatonin and other hormones, and many other rhythms, allostasis should be a more accurate concept than homeostasis (remaining stable by staying the same). Although there is no evidence at present to show that redox *in vivo* remains stable by being variable, numerous studies have suggested that the increased formation of ROS, whether induced by aging, exercise, or other stress conditions, is initiated to re-establish "redox homeostasis" (for review, see [129]). From a rigorous scientific point of view, the term "redox homeostasis" used here should be replaced by "redox allostasis".

Based on the multi-point property of allostasis, we have postulated the allostatic system as a special "buffering system": it has a basal level and certain buffering capacity that can maintain dynamic stability. Therefore, we have coined the term "allostatic buffering capacity (ABC)" with five components: basal level, peak level, buffering range, increase rate and recovery rate, to give a good picture of the capacity of an allostatic system to maintain dynamic stability. The action model of exercise on ABC has also been addressed. For more details, readers are recommended to read our review published in 2009 [130].

#### *6.2.2. Present evidence of exercise-induced ROS to enhance redox ABC*

Regular exercise can promote mitochondrial biogenesis and enhance muscle oxidative capacity [180, 181], and the molecular signals are mainly the increased ROS, such as H2O2 [180, 181]. In addition, exercise training has been reported to decrease ROS production through reducing the electronic leakage with better-regulated mitochondrial electron-transport chain [182] and a larger pool of functional mitochondria [183], which is critical to maintain health and delay the onset and progressive course of some diseases [184]. Moreover, the SOD activity has consistently been shown to increase with exercise in an intensity-dependent manner [185]. Long-term athletic training can increase the activity of proteasome complexes, which increase the degradation and turnover rate of oxidative modified proteins [186].

and transient high levels of ROS induced by physical exercise will introduce eustress *in vivo* and contribute to the hormesis-induced ABC enhancement, which benefits physical fitness. Further work is needed to substantiate the exact mechanisms of ROS in physical fitness.

> **After strenuous exercise**

**Endogenous or exogenous antioxidant defences**

http://dx.doi.org/10.5772/53360

185

**Enzymatic systems:** 

The Positive and Negative Aspects of Reactive Oxygen Species in Sports Performance

SODs, catalase, peroxidases, *etc.* **Non-enzymatic systems:**

carotene, polyphenols, *etc.*

NAC, thiols, vitamin C, vitamin E, β-

**Impaired physical fitness** 

**Accelerated aging / morbidity / mortality** 

**Cells in the immune system**

**Tissue damage**

**During or after strenuous exercise** 

**Energy depletion or Ischemia-reperfusion**

**Xanthine oxidase**

**During moderate exercise**

**Mitochondria**

**Weakened physical** 

**Promoted aging / morbidity / mortality**

**Acknowledgements**

ment.

**Aerobic metabolism**

**ROS**

**Less Adequate Optimal More**

**Weakened redox ABC Normal redox ABC Enhanced redox ABC Impaired redox ABC** 

**Figure 1. The sources and potential effects of reactive oxygen species (ROS)**. During or after exercise, ROS are generated as a result of aerobic metabolism in mitochondria, as well as from the activation of xanthine oxidase (XO). In addition, a variety of cells in the immune system can contribute to ROS production. A sophisticated enzymatic and non-enzymatic antioxidant defence system regulates overall ROS levels. Adequate ROS levels are necessary to main‐ tain redox allostatic buffering capacity (ABC). Optimal higher levels of ROS can enhance redox ABC, which improves physical fitness and subsequently delays the aging process and reduces morbidity or mortality of all-cause diseases. Lowering ROS levels below the allostatic set point may interrupt the physiological role of ROS in maintaining redox ABC and cellular adaption to exercise. Similarly, an excessive rise in ROS levels may also constitute a stress signal that

Very grateful to Dr. Dazhong Yin and Ms. Fang Lei for their constructive suggestions during preparation of the paper. This work has been supported by National Science Funds of China (30800207, 31271257) and Scientific Research Funds of Hunan Provincial Education Depart‐

**fitness** 

**Decelerated aging / morbidity / mortality**

**fitness Normal physical fitness Enhanced physical** 

**Normal aging / morbidity / mortality** 

damages redox ABC, and ultimately accelerate the aging process and age-related diseases.

These findings indicate that regular exercise can enhance the redox ABC through: (a) lowering the basal ROS level by reducing ROS production, decreasing resting respiration rate and reestablishing redox allostasis, (b) increasing the peak level and oxidative buffering range by promoting mitochondrial biogenesis, and (c) decreasing the oxidative stress rate and increas‐ ing recovery rate by re-establishing redox allostasis and enhancing the antioxidant defensive system and damage repair system. In contrast, intense and prolonged exercise may damage redox ABC.

## **7. Summary and perspectives**

Most currently available evidence clearly demonstrates that physical activity is associated with an increase of ROS generation in almost all studied cells, tissues and organs. There are many sites for producing ROS during or after exercise (Figure 1]. During moderate aerobic exercise, mitochondria are the predominant site for generating ROS. When energy depletion or ischemia-reperfusion occurs, especially during or after exhaustive exercise, XO may be an important site for ROS production. Macrophages, eosinophils, neutrophils and other cells in the immune system may also contribute to the ROS formation after exercise when tissue damage occurs. With the advance of analytical methods and techniques for assaying ROS *in situ*, more evidence would be produced to fully elucidate the mechanism and site of ROS formation during or after exercise.

ROS formation during exercise has dual effects. Based on the free radical theory of aging, ROS are toxic molecules due to their high reactivity to most biological macromolecules. Supple‐ mentation with antioxidants should offer some preventive effects against exercise-induced oxidative damage, and improve muscular function and physical performance. However, growing evidence shows that exercise-induced ROS may act as signalling molecules to mediate useful cellular adaption to exercise, mainly through regulating the expression of cytoprotective proteins and/or several redox-sensitive transcription factors. Although the supplementation of antioxidants may attenuate exercise-induced oxidative stress, there is insufficient evidence that it protects against exercise-induced muscular function damage or exercise performance.

Combined with the hormetic characteristic of exercise-induced ROS and the property of allostasis, hormesis-induced ABC enhancement should be a physiological mechanism to explain ROS-induced physical fitness (Figure 1). Different intensities or types of physical exercise would cause different levels of ROS generation. Too-small or too-large ROS will introduce too-weak eustress ("good stress") or too-strong distress ("bad stress") and result in allostasis load through weakening ABC or damaging ABC, respectively. However, moderate and transient high levels of ROS induced by physical exercise will introduce eustress *in vivo* and contribute to the hormesis-induced ABC enhancement, which benefits physical fitness. Further work is needed to substantiate the exact mechanisms of ROS in physical fitness.

**Figure 1. The sources and potential effects of reactive oxygen species (ROS)**. During or after exercise, ROS are generated as a result of aerobic metabolism in mitochondria, as well as from the activation of xanthine oxidase (XO). In addition, a variety of cells in the immune system can contribute to ROS production. A sophisticated enzymatic and non-enzymatic antioxidant defence system regulates overall ROS levels. Adequate ROS levels are necessary to main‐ tain redox allostatic buffering capacity (ABC). Optimal higher levels of ROS can enhance redox ABC, which improves physical fitness and subsequently delays the aging process and reduces morbidity or mortality of all-cause diseases. Lowering ROS levels below the allostatic set point may interrupt the physiological role of ROS in maintaining redox ABC and cellular adaption to exercise. Similarly, an excessive rise in ROS levels may also constitute a stress signal that damages redox ABC, and ultimately accelerate the aging process and age-related diseases.

## **Acknowledgements**

reducing the electronic leakage with better-regulated mitochondrial electron-transport chain [182] and a larger pool of functional mitochondria [183], which is critical to maintain health and delay the onset and progressive course of some diseases [184]. Moreover, the SOD activity has consistently been shown to increase with exercise in an intensity-dependent manner [185]. Long-term athletic training can increase the activity of proteasome complexes, which increase

These findings indicate that regular exercise can enhance the redox ABC through: (a) lowering the basal ROS level by reducing ROS production, decreasing resting respiration rate and reestablishing redox allostasis, (b) increasing the peak level and oxidative buffering range by promoting mitochondrial biogenesis, and (c) decreasing the oxidative stress rate and increas‐ ing recovery rate by re-establishing redox allostasis and enhancing the antioxidant defensive system and damage repair system. In contrast, intense and prolonged exercise may damage

Most currently available evidence clearly demonstrates that physical activity is associated with an increase of ROS generation in almost all studied cells, tissues and organs. There are many sites for producing ROS during or after exercise (Figure 1]. During moderate aerobic exercise, mitochondria are the predominant site for generating ROS. When energy depletion or ischemia-reperfusion occurs, especially during or after exhaustive exercise, XO may be an important site for ROS production. Macrophages, eosinophils, neutrophils and other cells in the immune system may also contribute to the ROS formation after exercise when tissue damage occurs. With the advance of analytical methods and techniques for assaying ROS *in situ*, more evidence would be produced to fully elucidate the mechanism and site of ROS

ROS formation during exercise has dual effects. Based on the free radical theory of aging, ROS are toxic molecules due to their high reactivity to most biological macromolecules. Supple‐ mentation with antioxidants should offer some preventive effects against exercise-induced oxidative damage, and improve muscular function and physical performance. However, growing evidence shows that exercise-induced ROS may act as signalling molecules to mediate useful cellular adaption to exercise, mainly through regulating the expression of cytoprotective proteins and/or several redox-sensitive transcription factors. Although the supplementation of antioxidants may attenuate exercise-induced oxidative stress, there is insufficient evidence that it protects against exercise-induced muscular function damage or exercise performance. Combined with the hormetic characteristic of exercise-induced ROS and the property of allostasis, hormesis-induced ABC enhancement should be a physiological mechanism to explain ROS-induced physical fitness (Figure 1). Different intensities or types of physical exercise would cause different levels of ROS generation. Too-small or too-large ROS will introduce too-weak eustress ("good stress") or too-strong distress ("bad stress") and result in allostasis load through weakening ABC or damaging ABC, respectively. However, moderate

the degradation and turnover rate of oxidative modified proteins [186].

redox ABC.

**7. Summary and perspectives**

184 Current Issues in Sports and Exercise Medicine

formation during or after exercise.

Very grateful to Dr. Dazhong Yin and Ms. Fang Lei for their constructive suggestions during preparation of the paper. This work has been supported by National Science Funds of China (30800207, 31271257) and Scientific Research Funds of Hunan Provincial Education Depart‐ ment.

## **List of abbreviations**

ROS: reactive oxygen species TBARS: thiobarbituric acid reactive substances MDA: malondialdehyde ESR: electron spin resonance EPR: electron paramagnetic resonance NO: nitric oxide BDNF: brain-derived neurotrophic factor UCP2: uncoupling protein 2 COPD: chronic obstructive pulmonary disease ATP: adenosine triphosphate XO: xanthine oxidase NFκB: nuclear factor kappaB NAC: N-acetylcysteine ABC: allostatic buffering capacity

## **Author details**

Guolin Li\*

Address all correspondence to: hnsdlgl@hunnu.edu.cn

College of Life Sciences, Hunan Normal University, Changsha, Hunan, China

## **References**

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pausal women with elevated blood pressure: a randomized controlled trial. JAMA:

The Positive and Negative Aspects of Reactive Oxygen Species in Sports Performance

http://dx.doi.org/10.5772/53360

187

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[2] Church TS, Earnest CP, Skinner JS, Blair SN. Effects of different doses of physical ac‐ tivity on cardiorespiratory fitness among sedentary, overweight or obese postmeno‐ pausal women with elevated blood pressure: a randomized controlled trial. JAMA: The Journal of the American Medical Association. 2007;297(19):2081-91.

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**List of abbreviations**

MDA: malondialdehyde

NO: nitric oxide

ROS: reactive oxygen species

186 Current Issues in Sports and Exercise Medicine

ESR: electron spin resonance

UCP2: uncoupling protein 2

ATP: adenosine triphosphate

NFκB: nuclear factor kappaB

ABC: allostatic buffering capacity

1995;273(14):1093-8.

XO: xanthine oxidase

NAC: N-acetylcysteine

**Author details**

Guolin Li\*

**References**

EPR: electron paramagnetic resonance

BDNF: brain-derived neurotrophic factor

COPD: chronic obstructive pulmonary disease

Address all correspondence to: hnsdlgl@hunnu.edu.cn

College of Life Sciences, Hunan Normal University, Changsha, Hunan, China

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[2] Church TS, Earnest CP, Skinner JS, Blair SN. Effects of different doses of physical ac‐ tivity on cardiorespiratory fitness among sedentary, overweight or obese postmeno‐

TBARS: thiobarbituric acid reactive substances


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**Chapter 7**

**Real and Simulated Altitude Training and Performance**

The use of altitude training to compliment normal training at sea level is widely used by coaches and athletes. There are a number of different altitude training models which range from living and training at moderate and high altitude to breathing hypoxic gas while living and training normally at sea level. In this chapter we will briefly overview the history of alti‐ tude training and touch on the science and practice of the various models of altitude train‐ ing. We also discuss the beneficial effects reported in the scientific literature and give firsthand accounts of the effectiveness of the various methods from high performance coaches. Benefits and drawbacks from each altitude method will be discussed along with advice on

Approximately 80% of the world's population lives at low altitude (< 500 m) [1] which has an optimal atmospheric pressure and oxygen concentration for the human body's function‐ ing. However as we ascend in altitude, the air volume expands due to the lowering of at‐ mospheric pressure, which results in the reduction of oxygen availability to the muscles. This drop in oxygen concentration results in decreased oxygen pressure in the inspired air (PIO2) and a subsequent drop in the amount of oxygen in the arterial blood (PaO2). A reduc‐ tion in the concentration of oxygen in the circulating arterial blood results in a decreased ability to extract oxygen for the working muscles and a reduced oxygen uptake. This re‐ duced oxygen uptake is a major problem for mountaineers at high altitude and is responsi‐ ble for the steady decline in maximal oxygen uptake (V˙ O2 max) and subsequent performance at high altitude. Traditional altitude training uses these oxygen concentration changes that occur with changes in elevation to induce beneficial adaptations in the per‐

Aviation physiology research has contributed significantly to the understanding of how the human body responds and adapts to a hypoxic (low oxygen concentration) environment. In

> © 2013 Hamlin et al.; licensee InTech. This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use,

© 2013 Hamlin et al.; licensee InTech. This is a paper distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

distribution, and reproduction in any medium, provided the original work is properly cited.

Michael J. Hamlin, Nick Draper and John Hellemans

Additional information is available at the end of the chapter

preparing athletes prior to altitude training.

formance of athletes either at altitude or closer to sea level.

http://dx.doi.org/10.5772/53724

**1. Introduction**

