Effects of prior exercise and a low-carbohydrate diet on muscle sarcoplasmic reticulum function during cycling in women

被引:19
作者
Duhamel, T. A. [1 ]
Green, H. J. [1 ]
Perco, J. G. [1 ]
Ouyang, J. [1 ]
机构
[1] Univ Waterloo, Dept Kinesiol, Waterloo, ON N2L 3G1, Canada
关键词
Ca2+ release; Ca2+ uptake; Ca2+ -ATPase activity; vastus lateralis; submaximal; female;
D O I
10.1152/japplphysiol.00052.2006
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The effects of exercise and diet on sarcoplasmic reticulum Ca2+-cycling properties in female vastus lateralis muscle were investigated in two groups of women following four different conditions. The conditions were 4 days of a low-carbohydrate (Lo CHO) and glycogen-depleting exercise plus a Lo CHO diet ( Ex + Lo CHO) ( experiment 2) and 4 days of normal CHO ( Norm CHO) and glycogen-depleting exercise plus Norm CHO ( Ex + Norm CHO) ( experiment 1). Peak aerobic power (Vo(2) (peak)) was 38.1 +/- 1.4 (SE); n = 9 and 35.6 +/- 1.4 ml (.) kg(-1) (.) min (-1); n = 9, respectively. Sarcoplasmic reticulum properties measured in vitro in homogenates (mu mol (.) g protein(-1) (.) min(-1)) indicated exercise-induced reductions ( P < 0.05) in maximal Ca2+-ATPase activity (0 > 30, 60 min > fatigue), Ca2+ uptake (0 > 30 > 60 min, fatigue), and Ca2+ release, both phase 1 (0 > 30 > 60 min, fatigue) and phase 2 (0 > 30, 60 min, fatigue; 30 min > fatigue) in Norm CHO. Exercise was without effect in altering the Hill slope (n(H)), defined as the slope of relationship between Ca2+-ATPase activity and Ca2+ concentration. No differences were observed between Norm CHO and Ex + Norm CHO. Compared with Norm CHO, Lo CHO resulted in a lower (P < 0.05) Ca2+ uptake, phase 1 Ca2+ release (0 > 30 min), and nH. Ex + Lo CHO resulted in a greater ( P < 0.05) Ca2+ uptake and nH compared with Lo CHO. The results demonstrate that Lo CHO alone can disrupt SR Ca2+ cycling and that, with the exception of Ca2+ release, a glycogen-depleting session of exercise before Lo CHO can reverse the effects.
引用
收藏
页码:695 / 706
页数:12
相关论文
共 51 条
[1]   DIET MUSCLE GLYCOGEN AND PHYSICAL PERFORMANCE [J].
BERGSTROM, J ;
HERMANSEN, L ;
HULTMAN, E ;
SALTIN, B .
ACTA PHYSIOLOGICA SCANDINAVICA, 1967, 71 (2-3) :140-+
[2]  
BERGSTROM J, 1962, SCAND J CLIN LAB INV, V14, P1
[3]   Impaired calcium pump function does not slow relaxation in human skeletal muscle after prolonged exercise [J].
Booth, J ;
McKenna, MJ ;
Ruell, PA ;
Gwinn, TH ;
Davis, GM ;
Thompson, MW ;
Harmer, AR ;
Hunter, SK ;
Sutton, JR .
JOURNAL OF APPLIED PHYSIOLOGY, 1997, 83 (02) :511-521
[4]   EFFECTS OF EXERCISE OF VARYING DURATION ON SARCOPLASMIC-RETICULUM FUNCTION [J].
BYRD, SK ;
BODE, AK ;
KLUG, GA .
JOURNAL OF APPLIED PHYSIOLOGY, 1989, 66 (03) :1383-1389
[5]   Effects of reduced muscle glycogen concentration on force, Ca2+ release and contractile protein function in intact mouse skeletal muscle [J].
Chin, ER ;
Allen, DG .
JOURNAL OF PHYSIOLOGY-LONDON, 1997, 498 (01) :17-29
[6]   GLYCOGEN PHOSPHOROLYSIS CAN FORM A METABOLIC SHUTTLE TO SUPPORT CA2+ UPTAKE BY SARCOPLASMIC-RETICULUM MEMBRANES IN SKELETAL-MUSCLE [J].
CUENDA, A ;
NOGUES, M ;
GUTIERREZMERINO, C ;
DEMEIS, L .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1993, 196 (03) :1127-1132
[7]   MODULATION BY PHOSPHORYLATION OF GLYCOGEN PHOSPHORYLASE-SARCOPLASMIC RETICULUM INTERACTION [J].
CUENDA, A ;
CENTENO, F ;
GUTIERREZMERINO, C .
FEBS LETTERS, 1991, 283 (02) :273-276
[8]   INTERACTION BETWEEN GLYCOGEN-PHOSPHORYLASE AND SARCOPLASMIC-RETICULUM MEMBRANES AND ITS FUNCTIONAL IMPLICATIONS [J].
CUENDA, A ;
NOGUES, M ;
HENAO, F ;
GUTIERREZMERINO, C .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (20) :11998-12004
[9]   The creatine kinase system is essential for optimal refill of the sarcoplasmic reticulum Ca2+ store in skeletal muscle [J].
de Groof, AJC ;
Fransen, JAM ;
Errington, RJ ;
Willems, PHGM ;
Wieringa, B ;
Koopman, WJH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (07) :5275-5284
[10]   Metabolic and sarcoplasmic reticulum Ca2+ cycling responses in human muscle 4 days following prolonged exercise [J].
Duhamel, TA ;
Green, HJ ;
Perco, JG ;
Ouyang, J .
CANADIAN JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY, 2005, 83 (07) :643-655