Skip to main content
Log in

Do invading leucocytes contribute to the decrease in glutathione concentrations indicating oxidative stress in exercised muscle, or are they important for its recovery?

  • Original Articles
  • Published:
European Journal of Applied Physiology and Occupational Physiology Aims and scope Submit manuscript

Abstract

Mice were subjected to one session of strenuous running exercise and their soleus muscles were examined in respect of changes in ultrastructure and to their concentration of reduced glutathione [GSH] which are indicators of oxidative stress. It was hypothesized that invading leucocytes contributed to oxidative stress and they were functionally inhibited in one experimental group by the administration of colchicine. Exercise led to an immediate decrease in [GSH] of about 60%, which slowly recovered during 96 h after exercise. With the administration of colchicine after exercise, [GSH] was higher than in the untreated exercise group 48 h after exercise, indicating an inhibition of the ability of leucocytes to produce oxidative stress. However, at 96 h after exercise, [GSH] was lower in the treated exercise group than in the untreated group. The morphological evaluation of the percentage of affected fibres showed that the invasion of leucocytes increased muscle fibre damage. The results suggested that invading leucocytes enhanced production of reactive species of oxygen that may have participated in inducing muscle damage. However, inhibition of leucocyte invasion did not permit their scavenger action of removing cell debris, which appeared to produce even more oxidative stress in the muscle.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Alessio H, Goldfarb A (1988) Lipid peroxidation and scavenger enzymes during exercise: adaptative response to training. J Appl Physiol 64:1333–1336

    Google Scholar 

  • Appell HJ, Soares JM, Duarte JA (1992) Exercise, muscle damage and fatigue. Sports Med 13:108–115

    Google Scholar 

  • Armstrong RB (1990) Initial events in exercise-induced muscular injury. Med Sci Sports Exerc 22:429–435

    Google Scholar 

  • Armstrong RB, Ogilvie RW, Schwane JA (1983) Eccentric exercise-induced injury to rat skeletal muscle. J Appl Physiol 54:80–93

    Google Scholar 

  • Bousquet E, Santagati NA, Lancetta T (1989) Determination of glutathione in biological tissues by high-performance liquid chromatography with electrochemical detection. J Pharmacol Biomed Anal 7:643–647

    Google Scholar 

  • Cannon JG, Orencole SF, Fielding RA, Meydani M, Meydani SN, Fiatarone MA, Blumberg JB, Evans WJ (1990) Acute phase response in exercise: interaction of age and vitamin E on neutrophils and muscle enzyme release. Am J Physiol 28:R1214-R1219

    Google Scholar 

  • Cochrane C (1991) Cellular injury by oxidants. Am J Med 91 [Suppl 3C]:23S-30S

    Google Scholar 

  • Dargel R (1992) Lipid peroxidation — a common pathogenetic mechanisms? Exp Toxicol Pathol 44:169–181

    Google Scholar 

  • Duarte JA, Soares JMC, Appell HJ (1992) Nifedipine diminishes exercise-induced muscle damage in mouse. Int J Sports Med 13:274–277

    Google Scholar 

  • Evans WJ, Cannon JG (1991) The metabolic effects of exerciseinduced muscle damage. In: Holloszy J (ed) Exercise and sports sciences reviews, vol. 19. Williams and Wilkins, Baltimore, pp 99–125

    Google Scholar 

  • Ferrari R, Ceconi C, Curello S, Cargnoni A, Alfieri O, Pardini A, Marzollo P, Visioli O (1991) Oxygen free radicals and myocardial damage: protective role of thiol-containing agents. Am J Med 91 [Suppl 3c]:95S-105S

    Google Scholar 

  • Hammeren J, Powers S, Lawler J, Criswell D, Martin D, Lowenthal D, Pollock M (1992) Exercise training-induced alterations in skeletal muscle oxidative and antioxidant enzyme activity in senescent rats. Int J Sports Med 13:412–416

    Google Scholar 

  • Henson PM, Johnston RB (1987) Tissue injury in inflamation. J Clin Invest 79:669–664

    Google Scholar 

  • Jenkins RR (1988) Free radical chemistry. Relationship to exercise. Sports Med 5:156–170

    Google Scholar 

  • Kondo Y, Honda S, Nakajima M, Miyahana K, Hayashi M, Shinagawa Y, Sato S, Inoue K, Nito S, Ariyuki F (1992) Micronucleus test with vincristine sulfate and colchicine in peripheral blood reticulolytes of mice using acridine orange supravital staining. Mutat Res 278:187–191

    Google Scholar 

  • Kuipers H, Drukker J, Frederik PM, Geurten P, Von Kranenburg G (1983) Muscle degeneration after exercise in rats. Int J Sports Med 4:45–51

    Google Scholar 

  • Laughlin MH, Simpson T, Sexton WL, Browns OR, Smith JK, Korthuis RJ (1990) Skeletal muscle oxidative capacity, antioxidant enzymes, and exercise training. J Appl Physiol 68:2337–2343

    Google Scholar 

  • Lew H, Pyke S, Quintanilha A (1985) Role of liver in exerciseinduced increases in plasma concentrations of reduced glutathione in rats. FEBS Lett 185:262–266

    Google Scholar 

  • Lew H, Pyke S, Quintanilha A (1987) The effects of physical exercise on the antioxidative capacity of the liver. Bioelectrochem Bioenerg 18:231–246

    Google Scholar 

  • Newham DJ, Jones DA, Clarkson PM (1987) Repeated highforce eccentric exercise: effects on muscle pain and damage. J Appl Physiol 63:1381–1386

    Google Scholar 

  • Numan I, Hassan M, Stohs S (1990) Protective effects of antioxidants against endrin-induced lipid peroxidation, glutathione depletion, and lethality in rats. Arch Environ Contam Toxicol 19:302–306

    Google Scholar 

  • Quintanilha A (1988) Oxidative effects of physical exercise. In: Quintanilha A (ed) Reactive oxygen species in chemistry, biology, and medicine. Plenum Press, New York, pp 187–195

    Google Scholar 

  • Reed DJ (1990) Glutathione: toxicological implications. Ann Rev Pharmacol Toxicol 30:603–631

    Google Scholar 

  • Salminen A (1985) Lysosomal changes in skeletal muscle during the repair of exercise injuries in muscle fibres. Acta Physiol Scand [Suppl] 539:1–31

    Google Scholar 

  • Salminen A, Vihko V (1983a) Lipid peroxidation in exercise myopathy. Exp Mol Pathol 38:380–388

    Google Scholar 

  • Salminen A, Vihko V (1983b) Endurance training reduces the susceptibility of mouse skeletal muscle to lipid peroxidation in vitro. Acta Physiol Scand 117:109–113

    Google Scholar 

  • Schmalbruch H (1976) The morphology of regeneration of skeletal muscles in the rat. Tissue Cell 8:673–692

    Google Scholar 

  • Starnes J, Cantu G, Farrrar R, Kehrer J (1989) Skeletal muscle lipid peroxidation in exercised and food-restricted rats during aging. J Appl Physiol 67:69–75

    Google Scholar 

  • Stauber WT, Fritz VK, Vogelbach DW, Dahlmann B (1988) Characterization of muscles injured by forced lengthening. I. Cellular infiltrates. Med Sci Sports Exerc 20:345–353

    Google Scholar 

  • Uhlig S, Wendel A (1992) The physiological consequences of glutathione variations. Life Sci 51:1083–1094

    Google Scholar 

  • Wallace SL, Omokoku B, Ertel NH (1970) Colchicine plasma levels. Implications as to pharmacology and mechanism of action. Am J Med 48:443–448

    Google Scholar 

  • Weiss SJ (1986) Oxygen, ischemia and inflammation. Acta Physiol Scand [Suppl] 584:9–37

    Google Scholar 

  • Zerba E, Komorowski TE, Faulkner JA (1990) Free radical injury to skeletal muscles of young, adult and old mice. Am J Physiol 258:C429-C435

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Duarte, J.A., Carvalho, F., Bastos, M.L. et al. Do invading leucocytes contribute to the decrease in glutathione concentrations indicating oxidative stress in exercised muscle, or are they important for its recovery?. Europ. J. Appl. Physiol. 68, 48–53 (1994). https://doi.org/10.1007/BF00599241

Download citation

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00599241

Key words

Navigation