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工作跳跃中葡萄糖灌注大鼠心脏代谢的计算机模拟。

Computer simulation of metabolism of glucose-perfused rat heart in a work-jump.

作者信息

Achs M J, Garfinkel D, Opie L H

出版信息

Am J Physiol. 1982 Sep;243(3):R389-99. doi: 10.1152/ajpregu.1982.243.3.R389.

Abstract

A computer model of glycolysis, the tricarboxylic acid cycle, and related amino acid metabolism, is described for a glucose-perfused experimental rat heart preparation suddenly switched from low work load (Langendorff perfusion) to high work load (left atrial perfusion). Glycolytic intermediate measurements suggest activation of phosphofructokinase within a few seconds. This activation, and also that of other glycolytic enzymes, is calculated as due to a sharp increase in cytoplasmic Mg2+ level, which overcomes the inhibitory effects of a rapid fall in cytoplasmic pH to 6.77 (calculated from a rapid fall in creatine phosphate). Increased glycolytic substrate is initially supplied by glycogenolysis mediated by phosphorylase b (activated by an early rise in cytoplasmic AMP), followed by increased glucose uptake from the perfusate. Testable predictions are made by the model, especially that lactate production rate should peak early. Additional experiments are described that verify these predictions and fill gaps in the original measurements. The role of modeling in interpreting such experiments is discussed.

摘要

本文描述了一个关于糖酵解、三羧酸循环及相关氨基酸代谢的计算机模型,该模型针对的是一个葡萄糖灌注的实验大鼠心脏标本,该标本突然从低工作负荷(Langendorff灌注)切换至高工作负荷(左心房灌注)。糖酵解中间产物的测量结果表明,磷酸果糖激酶在几秒钟内被激活。这种激活以及其他糖酵解酶的激活,据计算是由于细胞质中Mg2+水平急剧上升所致,这克服了细胞质pH值迅速降至6.77(根据磷酸肌酸的迅速下降计算得出)所产生的抑制作用。增加的糖酵解底物最初由磷酸化酶b介导的糖原分解提供(由细胞质中AMP的早期升高激活),随后是从灌注液中摄取更多葡萄糖。该模型做出了可检验的预测,特别是乳酸产生率应在早期达到峰值。文中还描述了额外的实验,这些实验验证了这些预测并填补了原始测量中的空白。讨论了建模在解释此类实验中的作用。

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