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[血管再通的犬心脏梗死区和梗死前区游离核苷酸及多胺的比活性和含量变化]

[Changes in the specific activity and content of free nucleotides and polyamines of the infarct and pre-infarct area of the revascularized dog heart].

作者信息

Casti A, Reali N, Corsi M, Pasquinelli V

出版信息

Ateneo Parmense Acta Biomed. 1975 May-Jun;46(3):135-47.

PMID:1156462
Abstract

Changes on specific radioactivity and levels of free nucleotides and polyamines in infarcted and borderline tissue of reperfused dog heart. The changes on specific radioactivity and levels of free nucleotides and polyamines, spermine and spermidine, of reperfused heart show a different behaviour of the anoxic myocardium. An increase of both specific activity and levels of free nucleotides and polyamines after 30 minutes of ischemia is observed. A longer period of anoxia (6 hours) causes a decreased synthesis and concentration of free nucleotides and polyamines. A remarkable recovery of specific activity of these compounds after reperfusion is noted. The borderline tissue shows a similar behaviour but with smaller changes. Therefore, in our experimental conditions, ischemia does not cause an irreversible alteration in protein synthesis mechanism of myocardial cells. In addition, the reperfusion may cause a recovery of biochemical mechanisms that control the functional capacity of the cell. The polyamine changes may postulate a central role of these amines in both anoxic and reperfused heart.

摘要

再灌注犬心脏梗死及边缘组织中比放射性、游离核苷酸和多胺水平的变化。再灌注心脏的比放射性、游离核苷酸和多胺(精胺和亚精胺)水平的变化显示出缺氧心肌的不同行为。缺血30分钟后观察到游离核苷酸和多胺的比活性及水平均增加。较长时间的缺氧(6小时)会导致游离核苷酸和多胺的合成及浓度降低。再灌注后这些化合物的比活性有显著恢复。边缘组织表现出类似行为,但变化较小。因此,在我们的实验条件下,缺血不会导致心肌细胞蛋白质合成机制发生不可逆改变。此外,再灌注可能导致控制细胞功能能力的生化机制恢复。多胺的变化可能表明这些胺类在缺氧和再灌注心脏中都起着核心作用。

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