Regulation of pyruvate dehydrogenase complex activity during myocardial ischemia.

Advances in myocardiology Pub Date : 1985-01-01
T C Vary, P J Randle
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Abstract

The effect of ischemia on the concentration of active pyruvate dehydrogenase (PDH) complex has been investigated in glucose-perfused hearts of normal rats fed a normal diet or a high-fat diet or starved for 48 hr and in hearts from alloxan-diabetic rats. Global ischemia induced by low flow (approximately equal to 1 ml/min) lowered the concentration of active complex under most conditions employed. Parallel studies of the effect of anoxia and of potassium arrest of the heart indicated that the effect of low-flow ischemia may result from decreased mechanical activity of the heart as a consequence of tissue hypoxia; the enzymatic mechanism may be activation of PDH kinase by increased reduction of mitochondrial NAD. In hearts of normal rats fed a normal diet, global ischemia induced by zero flow increased the concentration of active complex. Evidence is given that this may result from a combination of anoxia and acidosis. In aerobic perfusions, concentrations of active complex were ranked in the order: normal diet greater than high-fat diet greater than 48-hr starved greater than alloxan-diabetic. This order was maintained when the concentration of active complex was lowered by global ischemia induced by zero flow.

心肌缺血时丙酮酸脱氢酶复合物活性的调节。
研究了在正常饮食或高脂肪饮食或饥饿48小时的正常大鼠和四氧嘧啶糖尿病大鼠的心脏中,缺血对活性丙酮酸脱氢酶(PDH)复合物浓度的影响。在大多数情况下,低流量(约等于1 ml/min)引起的全身缺血降低了活性复合物的浓度。对心脏缺氧和钾停搏影响的平行研究表明,低流量缺血的影响可能是由于组织缺氧导致心脏机械活动下降所致;酶促机制可能是通过增加线粒体NAD的减少激活PDH激酶。在正常饮食的正常大鼠心脏中,零流量引起的全身缺血增加了活性复合物的浓度。有证据表明,这可能是由缺氧和酸中毒共同造成的。在有氧灌注中,活性复合物的浓度按顺序排列:正常饮食大于高脂肪饮食大于48小时饥饿大于四氧嘧啶糖尿病。当零流量引起的全身缺血降低活性复合物的浓度时,这一顺序仍保持不变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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