Constantin-Teodosiu D, Cederblad G, Hultman E
Department of Clinical Chemistry, Huddinge University Hospital, Karolinska Institute, Sweden.
J Appl Physiol (1985). 1992 Dec;73(6):2403-7. doi: 10.1152/jappl.1992.73.6.2403.
Seven subjects cycled to exhaustion [58 +/- 7 (SE) min] at approximately 75% of their maximal oxygen uptake (VO2max). Needle biopsy samples were taken from the quadriceps femoris muscle at rest, after 3, 10, and 40 min of exercise, at exhaustion, and after 10 min of recovery. After 3 min of exercise, a nearly complete transformation of the pyruvate dehydrogenase complex (PDC) into active form had occurred and was maintained throughout the exercise period. The total in vitro activated PDC was unchanged during exercise. The muscle concentration of acetyl-CoA increased from a resting value of 8.4 +/- 1.0 to 31.6 +/- 3.3 mumol/kg dry wt at exhaustion and that of acetylcarnitine from 2.9 +/- 0.7 to 15.6 +/- 1.6 mmol/kg dry wt. This was accompanied by corresponding decreases in reduced CoA (CoASH) from 45.3 +/- 3.1 to 25.9 +/- 3.1 mumol/kg dry wt and in free carnitine from 18.8 +/- 0.7 to 5.7 +/- 0.5 mmol/kg dry wt. Acetyl group accumulation, in the form of acetyl-CoA and acetylcarnitine, was maintained throughout exercise to exhaustion while the glycogen content decreased by 90%. This suggests that availability of acetyl groups was not limiting to exercise performance despite the nearly total depletion of the glycogen store. The increased acetyl-CoA-to-CoASH ratio during exercise caused inhibition of neither the PDC transformation nor the calculated catalytic activity of active PDC.
七名受试者以约75%的最大摄氧量(VO2max)进行自行车运动直至力竭[58±7(标准误)分钟]。在静息状态、运动3分钟、10分钟和40分钟后、力竭时以及恢复10分钟后,从股四头肌采集针吸活检样本。运动3分钟后,丙酮酸脱氢酶复合体(PDC)几乎完全转变为活性形式,并在整个运动期间保持。运动过程中体外总活性PDC不变。乙酰辅酶A的肌肉浓度从静息值8.4±1.0增加到力竭时的31.6±3.3μmol/kg干重,乙酰肉碱的浓度从2.9±0.7增加到15.6±1.6mmol/kg干重。与此同时,还原型辅酶A(CoASH)从45.3±3.1降至25.9±3.1μmol/kg干重,游离肉碱从18.8±0.7降至5.7±0.5mmol/kg干重。以乙酰辅酶A和乙酰肉碱形式存在的乙酰基积累在整个运动至力竭过程中持续存在,而糖原含量下降了90%。这表明尽管糖原储备几乎完全耗尽,但乙酰基的可用性并不限制运动表现。运动期间乙酰辅酶A与CoASH比值的增加既未抑制PDC的转变,也未抑制活性PDC的计算催化活性。