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钙通道阻滞剂对阿霉素处理的离体成年心肌细胞的急性作用。

Acute effect of calcium channel blockers on adriamycin exposed isolated adult cardiocytes.

作者信息

Maisch B, Gregor O, Zeuss M, Kochsiek K

出版信息

Basic Res Cardiol. 1985 Nov-Dec;80(6):626-35. doi: 10.1007/BF01907861.

Abstract

When tested with isolated, calcium-resistant resting rat cardiocytes in an in vitro assay system, adriamycin exerted a dose-dependent cytotoxic effect which could easily be assessed by the ATP depletion of the heart cells and the loss of vitality as monitored by morphological changes (blebbing, spherical contraction). Apart from extremely high non pharmacological concentrations of verapamil and diltiazem, both calcium antagonists left the cardiocytes intact and without loss of internal ATP when given alone to the medium. Coincubation of adriamycin and verapamil or diltiazem did not increase adriamycin toxicity to the cardiocytes; instead a remarkable ATP preservation by verapamil could be demonstrated when both drugs (adriamycin and verapamil) were incubated simultaneously with the heart cells. This acute protective effect was limited in time and could no longer be detected after 9 hours. Diltiazem in coincubation experiments exerted neither a toxic nor an acute protective effect on adriamycin-exposed heart cells.

摘要

在体外分析系统中,用分离出的对钙有抗性的静止大鼠心肌细胞进行测试时,阿霉素呈现出剂量依赖性细胞毒性作用,这可以通过心肌细胞的ATP耗竭以及通过形态学变化(起泡、球形收缩)监测的活力丧失来轻松评估。除了极高的非药理学浓度的维拉帕米和地尔硫䓬外,这两种钙拮抗剂单独加入培养基时,心肌细胞保持完整且内部ATP没有损失。阿霉素与维拉帕米或地尔硫䓬共同孵育不会增加阿霉素对心肌细胞的毒性;相反,当两种药物(阿霉素和维拉帕米)与心肌细胞同时孵育时,可以证明维拉帕米能显著保存ATP。这种急性保护作用在时间上是有限的,9小时后就不再能检测到。在共同孵育实验中,地尔硫䓬对暴露于阿霉素的心肌细胞既没有毒性作用也没有急性保护作用。

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