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强心药物的历史视角。

Historical perspectives on inotropic agents.

作者信息

Farah A E

出版信息

Circulation. 1986 Mar;73(3 Pt 2):III4-9.

PMID:3510779
Abstract

Although early experiments in animals and humans suggested that digitalis glycosides increased cardiac output only in the failing heart, later studies showed that these cardiotonic agents increase intraventricular systolic pressure and decrease relaxation time in the normal animal. The controversy concerning the peripheral vascular or direct cardiac effects of digitalis was finally resolved when new methods were applied to the study of the effects of this drug on intraventricular pressures and cardiac contractile force. Other positive inotropic agents, such as the adrenergic agonists, have also been tested for the treatment of heart failure. However, during long-term oral or intravenous therapy, the effectiveness of these drugs appears to diminish. Clinical studies of glucagon, a polypeptide with positive inotropic and chronotropic effects, have revealed its potential for causing side effects and its reduced activity in patients with chronic heart failure. With the discovery of several new types of inotropic agents, i.e., the bipyridines and the imidazole and benzimidazole derivatives, interest in revising our therapeutic approach to congestive heart failure has increased. This review discusses recent developments in this area.

摘要

尽管早期在动物和人体上进行的实验表明,洋地黄糖苷仅能增加衰竭心脏的心输出量,但后来的研究显示,这些强心剂能增加正常动物的心室内收缩压并缩短舒张时间。当新的方法被应用于研究洋地黄对心室内压和心脏收缩力的影响时,关于洋地黄的外周血管作用或直接心脏作用的争议最终得以解决。其他正性肌力药物,如肾上腺素能激动剂,也已被测试用于治疗心力衰竭。然而,在长期口服或静脉治疗期间,这些药物的有效性似乎会降低。对胰高血糖素(一种具有正性肌力和变时作用的多肽)的临床研究表明,它有引起副作用的可能性,且在慢性心力衰竭患者中的活性降低。随着几种新型正性肌力药物的发现,即双吡啶类以及咪唑和苯并咪唑衍生物,人们对修订我们治疗充血性心力衰竭的方法的兴趣增加了。这篇综述讨论了该领域的最新进展。

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