柠檬酸循环
生物化学
焊剂(冶金)
骨骼肌
丙酮酸羧化酶
柠檬酸合酶
糖酵解
代谢途径
新陈代谢
生物
磷酸烯醇式丙酮酸羧化酶
酶
丙酮酸脱氢酶复合物
化学
内分泌学
有机化学
作者
Martin J. Gibala,Martin E. Young,H. Taegtmeyer
出处
期刊:Acta Physiologica Scandinavica
[Wiley]
日期:2000-04-01
卷期号:168 (4): 657-665
被引量:169
标识
DOI:10.1046/j.1365-201x.2000.00717.x
摘要
Efficient energy transfer in heart and skeletal muscle requires a series of moiety‐conserved cycles. The intermediaries of the metabolic cycles are finely regulated to maintain a dynamic state of equilibrium. In heart muscle, depletion of the citric acid cycle (TCA cycle) through a block of 2‐oxoglutarate dehydrogenase results in a rapid decline of contractile function, which is reversed by the addition of substrates promoting flux through the carboxylating enzymes, malic enzyme, pyruvate carboxylase and propionyl‐CoA carboxylase. Anaplerosis describes a pathway, which replenishes a metabolic cycle. We show that enzymes for anaplerosis of the TCA cycle are expressed in heart and skeletal muscles. The role of anaplerosis of the TCA cycle in skeletal muscle is not entirely clear, but there is substantial evidence for its operational control during exercise. While the anaplerotic flux of carbon into the TCA cycle exceeds the removal of cycle intermediates, this process is only transient and reverses with prolonged exercise. It remains to be determined, however, whether the initial increase in TCA cycle intermediates is obligatory in order to attain high rates of TCA cycle flux, or primarily reflects a mass action phenomenon owing to increased substrate availability for anaplerotic pathways.
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