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正性肌力药物作用机制的选择性更新。

Selective updates on mechanisms of action of positive inotropic agents.

作者信息

Grupp G

机构信息

Department of Physiology and Biophysics, University of Cincinnati, College of Medicine, Ohio 45267.

出版信息

Mol Cell Biochem. 1987 Aug;76(2):97-112. doi: 10.1007/BF00223475.

Abstract

Several extensive reviews concerning the actions of new positive inotropic agents in the treatment of congestive heart failure, often with reference to their mechanism of action, have recently been published. Each of them has presented specific points of view. This review will place special emphasis on the significance of intracellular sodium activity for the modulation of myocardial inotropy; the continuing importance, after a 200 year history, of the use of cardiac glycosides as strong inotropic agents; the emerging significance of the phosphoinositide (PIP2) pathway to provide additional second messengers for the modulation and regulation of cardiac inotropy; the contribution of the alpha 1-adrenergic system to cardiac inotropy; the increasing awareness of the significant involvement of adenosine and its antagonists in cardiac function; and the increasing realization that myocardial tissues are not homogeneous, i.e., that in many species the atrial and ventricular tissues are using different, even opposite mechanisms in the generation of their functional responses.

摘要

最近发表了几篇关于新型正性肌力药物治疗充血性心力衰竭作用的广泛综述,这些综述常常涉及它们的作用机制。每一篇都提出了特定的观点。本综述将特别强调细胞内钠活性对心肌收缩力调节的重要性;经过200年的历史,强心苷作为强效正性肌力药物使用的持续重要性;磷酸肌醇(PIP2)途径对于为心肌收缩力的调节和调控提供额外第二信使的新出现的重要性;α1-肾上腺素能系统对心肌收缩力的贡献;对腺苷及其拮抗剂在心脏功能中显著参与的认识不断增加;以及越来越意识到心肌组织并非均质的,即,在许多物种中,心房和心室组织在产生其功能反应时使用不同甚至相反的机制。

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