Exercise training protects against contraction-induced lipid peroxidation in the diaphragm

被引:46
作者
Vincent, HK [1 ]
Powers, SK [1 ]
Demirel, HA [1 ]
Coombes, JS [1 ]
Naito, H [1 ]
机构
[1] Univ Florida, Ctr Exercise & Sport Sci, Gainesville, FL 32611 USA
关键词
fatigue; antioxidant enzymes; nonprotein thiols; lipid peroxidation; oxidative stress;
D O I
10.1007/s004210050505
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Endurance exercise training promotes a small but significant increase in antioxidant enzyme activity in the costal diaphragm (DIA) of rodents. It is unclear if these training-induced improvements in muscle antioxidant capacity are large enough to reduce oxidative stress during prolonged contractile activity. To test the hypothesis that training-related increases in DIA antioxidant capacity reduces contraction-induced lipid peroxidation. we exercise trained adult female Sprague-Dawley (n = 7) rats on a motor-driven treadmill for 12 weeks at approximate to 75% maximal O-2 consumption (90 min/day). Control animals (n = 8) remained sedentary during the same 12-week period. After training, DIA strips from animals in both experimental groups were excised and subjected to an in vitro fatigue contractile protocol in which the muscle was stimulated for 60 min at a frequency of 30 Hz, every 2 s with a train duration of 330 m. Compared to the controls, endurance training resulted in an increase (P < 0.05) in diaphragmatic non-protein thiols and in the activity of the antioxidant enzyme superoxide dismutase. Following. the contractile protocol, lipid peroxidation was significantly lower (P < 0.05) in the trained DIA compared to the controls. These data support the hypothesis that endurance exercise training-induced increases in DIA antioxidant capacity protect the muscle against contractile-related oxidative stress.
引用
收藏
页码:268 / 273
页数:6
相关论文
共 31 条
[1]   LIPID-PEROXIDATION AND SCAVENGER ENZYMES DURING EXERCISE - ADAPTIVE RESPONSE TO TRAINING [J].
ALESSIO, HM ;
GOLDFARB, AH .
JOURNAL OF APPLIED PHYSIOLOGY, 1988, 64 (04) :1333-1336
[2]   RESISTIVE BREATHING ACTIVATES THE GLUTATHIONE REDOX CYCLE AND IMPAIRS PERFORMANCE OF RAT DIAPHRAGM [J].
ANZUETO, A ;
ANDRADE, FH ;
MAXWELL, LC ;
LEVINE, SM ;
LAWRENCE, RA ;
GIBBONS, WJ ;
JENKINSON, SG .
JOURNAL OF APPLIED PHYSIOLOGY, 1992, 72 (02) :529-534
[3]   THE SPECTRAL DISTRIBUTION OF THE INTRINSIC RADIATIVE RECOMBINATION IN SILICON [J].
RUFF, M ;
FICK, M ;
LINDNER, R ;
ROSSLER, U ;
HELBIG, R .
JOURNAL OF APPLIED PHYSICS, 1993, 74 (01) :267-274
[4]   DETERMINATION OF METABOLIC AND HEART-RATE RESPONSES OF RATS TO TREADMILL EXERCISE [J].
BROOKS, GA ;
WHITE, TP .
JOURNAL OF APPLIED PHYSIOLOGY, 1978, 45 (06) :1009-1015
[5]   HYDROXYLATION OF SALICYLATE BY THE IN-VITRO DIAPHRAGM - EVIDENCE FOR HYDROXYL RADICAL PRODUCTION DURING FATIGUE [J].
DIAZ, PT ;
SHE, ZW ;
DAVIS, WB ;
CLANTON, TL .
JOURNAL OF APPLIED PHYSIOLOGY, 1993, 75 (02) :540-545
[6]  
DU Y, 1991, American Review of Respiratory Disease, V143, pA560
[7]  
FLOHE L, 1984, METHOD ENZYMOL, V105, P114
[8]   MUSCULAR ENLARGEMENT AND NUMBER OF FIBERS IN SKELETAL-MUSCLES OF RATS [J].
GOLLNICK, PD ;
TIMSON, BF ;
MOORE, RL ;
RIEDY, M .
JOURNAL OF APPLIED PHYSIOLOGY, 1981, 50 (05) :936-943
[9]  
GREEN H, 1986, J NEUROL SCI, V84, P157
[10]   EXTREME ENDURANCE TRAINING AND FIBER TYPE ADAPTATION IN RAT DIAPHRAGM [J].
GREEN, HJ ;
PLYLEY, MJ ;
SMITH, DM ;
KILE, JG .
JOURNAL OF APPLIED PHYSIOLOGY, 1989, 66 (04) :1914-1920