VO2 max is unaffected by altering the temporal pattern of stimulation frequency in rat hindlimb in situ

被引:14
作者
Hepple, RT
Krause, DJ
Hagen, JL
Jackson, CC
机构
[1] Univ Calgary, Fac Kinesiol, Calgary, AB T2N 1N4, Canada
[2] Univ Calgary, Fac Med, Calgary, AB T2N 1N4, Canada
关键词
maximal O-2 uptake; aerobic metabolism; anaerobic metabolism; lactate;
D O I
10.1152/japplphysiol.00058.2003
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
It might be anticipated that fatiguing contractions would impair the aerobic metabolic response in skeletal muscle if significant fatigue developed before full activation of aerobic metabolism. On the basis of this premise, we examined two groups of rats to test the hypothesis that a gradual increase in stimulation frequency would yield a higher maximal O-2 uptake ((V) over dot O-2 max) than beginning immediately with an intense stimulation frequency because of a slower progression of fatigue under the former conditions. In one group of animals, the distal hindlimb muscles were electrically stimulated at a frequency of 60 tetani/min for 4 min (F-60; n = 6 rats); in the other group, the muscles were incrementally stimulated for 1 min at each of 7.5, 15, 30, and 60 tetani/min and for 2 min at 90 tetani/ min (F-Inc; n = 5 rats). Despite large differences in rate of fatigue [time to 60% of initial force was 47 +/- 3 (SE) vs. 188 +/- 1 s in F-60 and F-Inc, respectively] and the time at which (V) over dot O-2 max occurred (120 +/- 15 vs. 264 +/- 6 s), (V) over dot O-2 max was not different (419 +/- 24 vs. 381 +/- 44 mumol . min(-1) . 100 g(-1)). Furthermore, time x tension integral at (V) over dot O-2 max (3.82 +/- 0.41 vs. 4.07 +/- 0.31 N . s) and peak lactate efflux ( 910 +/- 45 vs. 800 +/- 98 mumol . min(-1) . 100 g(-1)) were not different between groups. Thus our results show that the more rapid progression of fatigue in F60 did not compromise the aerobic metabolic response in electrically stimulated rat hindlimb muscles. However, in both groups, O-2 uptake and lactate efflux declined after (V) over dot O-2 max was attained in similar proportion to a further fall in force, suggesting that ongoing fatigue with intense contractions reduced ATP demand below that requiring maximal aerobic and glycolytic metabolic responses once (V) over dot O-2 max was reached.
引用
收藏
页码:705 / 711
页数:7
相关论文
共 29 条
[1]   PRELOAD RELEASE INCREASES BLOOD-FLOW AND DECREASES FATIGUE DURING REPETITIVE ISOTONIC MUSCLE CONTRACTIONS [J].
AMEREDES, BT ;
BRECHUE, WF ;
STAINSBY, WN .
JOURNAL OF APPLIED PHYSIOLOGY, 1994, 77 (06) :2641-2647
[2]  
ARMSTRONG RB, 1984, AM J ANAT, V171, P259, DOI 10.1002/aja.1001710303
[3]   MODELING THE EFFECTS OF HYPOXIA ON ATP TURNOVER IN EXERCISING MUSCLE [J].
ARTHUR, PG ;
HOGAN, MC ;
BEBOUT, DE ;
WAGNER, PD ;
HOCHACHKA, PW .
JOURNAL OF APPLIED PHYSIOLOGY, 1992, 73 (02) :737-742
[4]   THE EFFECTS ON THE RESPIRATION AND PERFORMANCE DURING EXERCISE OF ADDING OXYGEN TO THE INSPIRED AIR [J].
BANNISTER, RG ;
CUNNINGHAM, DJC .
JOURNAL OF PHYSIOLOGY-LONDON, 1954, 125 (01) :118-137
[5]   TRANSPORT OF ENERGY IN MUSCLE - THE PHOSPHORYLCREATINE SHUTTLE [J].
BESSMAN, SP ;
GEIGER, PJ .
SCIENCE, 1981, 211 (4481) :448-452
[6]   BLOOD-FLOW ELEVATION INCREASES VO2 MAXIMUM DURING REPETITIVE TETANIC CONTRACTIONS OF DOG MUSCLE INSITU [J].
BRECHUE, WF ;
AMEREDES, BT ;
ANDREW, GM ;
STAINSBY, WN .
JOURNAL OF APPLIED PHYSIOLOGY, 1993, 74 (04) :1499-1503
[7]   ANALYSIS OF METABOLIC CONTROL - NEW INSIGHTS USING SCALED CREATINE-KINASE MODEL [J].
CONNETT, RJ .
AMERICAN JOURNAL OF PHYSIOLOGY, 1988, 254 (06) :R949-R959
[8]   Inhibition of creatine kinase reduces the rate of fatigue-induced decrease in tetanic [Ca2+]i in mouse skeletal muscle [J].
Dahlstedt, AJ ;
Westerblad, H .
JOURNAL OF PHYSIOLOGY-LONDON, 2001, 533 (03) :639-649
[9]   Role of myoplasmic phosphate in contractile function of skeletal muscle: studies on creatine kinase-deficient mice [J].
Dahlstedt, AJ ;
Katz, A ;
Westerblad, H .
JOURNAL OF PHYSIOLOGY-LONDON, 2001, 533 (02) :379-388
[10]   CELLULAR MECHANISMS OF MUSCLE FATIGUE [J].
FITTS, RH .
PHYSIOLOGICAL REVIEWS, 1994, 74 (01) :49-94