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四氧嘧啶糖尿病大鼠离体灌注心脏的心脏功能

Cardiac performance of isolated perfused hearts from alloxan diabetic rats.

作者信息

Miller T B

出版信息

Am J Physiol. 1979 Jun;236(6):H808-12. doi: 10.1152/ajpheart.1979.236.6.H808.

Abstract

Acute alloxan diabetes (3 days) in the rat resulted in a decreased ability of the isolated perfused working heart to respond to increased atrial filling pressure with normal systolic (aortic) pressure development, using a physiologic concentration of glucose (5 mM) as substrate. The diabetic heart also exhibited impaired cardiac output, which could be attributed entirely to decreased aortic output without any apparent effect on coronary flow. This decrease in ventricular performance was accompanied by a 40% reduction in glucose uptake and a 20% reduction in tissue ATP concentrations even though perfusate glucose levels remained at or near physiologic levels. Perfusion of hearts with 5 mM glucose plus 10(-8) M insulin, with 10 or 30 mM glucose, or 1 mM octanoate reversed the diabetes-related decrease in systolic pressure development, cardiac output, and tissue ATP content. These data demonstrate that the defect in cardiac performance with increased work loads associated with acute insulin deficiency is due to the relative inability of the heart to utilize physiologic concentrations of glucose as substrate for energy production.

摘要

大鼠急性四氧嘧啶糖尿病(3天)导致离体灌注工作心脏在以生理浓度葡萄糖(5 mM)为底物时,对增加的心房充盈压产生正常收缩期(主动脉)压力的反应能力下降。糖尿病心脏还表现出心输出量受损,这完全可归因于主动脉输出减少,而对冠状动脉血流无明显影响。心室功能的这种下降伴随着葡萄糖摄取减少40%和组织ATP浓度降低20%,尽管灌注液葡萄糖水平保持在或接近生理水平。用5 mM葡萄糖加10(-8) M胰岛素、10或30 mM葡萄糖或1 mM辛酸灌注心脏可逆转与糖尿病相关的收缩压发展、心输出量和组织ATP含量的下降。这些数据表明,与急性胰岛素缺乏相关的工作负荷增加时心脏功能的缺陷是由于心脏相对无法利用生理浓度的葡萄糖作为能量产生的底物。

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