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缺血性心脏中碳水化合物和脂肪酸代谢的限速步骤。

Rate-limiting steps of carbohydrate and fatty acid metabolism in ischemic hearts.

作者信息

Neely J R, Rovetto M J, Whitmer J T

出版信息

Acta Med Scand Suppl. 1976;587:9-15. doi: 10.1111/j.0954-6820.1976.tb05861.x.

Abstract

Control of glycolysis and fatty acid oxidation in ischemic myocardium was studied in isolated working rat hearts. Coronary flow was reduced to the whole heart. In ischemic tissue, oxygen consumption, glycolysis and fatty acid oxidation all decreased in proportion to the restriction in coronary flow. Inhibition of glycolysis developed at the level of glyceraldehyde-3-phosphate dehydrogenase. Restricted flux through this step appeared to result from accumulation of lactate, H+ and NADH. The rate of glycolysis was inversely related to accumulation of lactate. Additions of high levels of lactate to the perfusate inhibited glycolysis in aerobic, anoxic and ischemic hearts. The mechanism of this effect of lactate in anaerobic hearts is unknown, but does not appear to be related to pH changes. Oxidation of fatty acids was restricted at the level of beta-oxidation and high levels of both long-chain acyl CoA and carnitine derivatives accumulated.

摘要

在离体工作大鼠心脏中研究了缺血心肌中糖酵解和脂肪酸氧化的调控。冠状动脉血流减少至整个心脏。在缺血组织中,耗氧量、糖酵解和脂肪酸氧化均与冠状动脉血流受限成比例下降。糖酵解在甘油醛-3-磷酸脱氢酶水平受到抑制。通过这一步骤的通量受限似乎是由于乳酸、H⁺和NADH的积累所致。糖酵解速率与乳酸积累呈负相关。向灌注液中添加高水平乳酸可抑制有氧、缺氧和缺血心脏中的糖酵解。乳酸在无氧心脏中的这种作用机制尚不清楚,但似乎与pH变化无关。脂肪酸氧化在β-氧化水平受到限制,长链酰基辅酶A和肉碱衍生物的高水平均积累。

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