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豚鼠心脏中的H1和H2受体:一项电生理学研究。

H1- and H2-receptors in the guinea-pig heart: an electrophysiological study.

作者信息

Amerini S, Franconi F, Ledda F, Mantelli L, Mugelli A

出版信息

Agents Actions. 1982 Apr;12(1-2):131-8. doi: 10.1007/BF01965123.

Abstract

The mechanical and electrophysiological effects of 2-pyridylethylamine (PEA) and 4-methylhistamine (4MeH) in different sections of guinea-pig heart were examined. 4MeH produced a dose-dependent increase in contractility in the right ventricle and the right atrium, and a decrease in functional refractory period (FRP) in all the sections studied; the action potential duration was decreased and the plateau phase was usually heightened in both atria and the ventricle. These effects were consistently antagonized by cimetidine. PEA-induced changes in contractility, FRP and the action potential profile were studied in the presence of cimetidine. Triprolidine antagonized PEA effects on FRP and the action potential profile only in the left atrium. The results obtained are discussed in terms of the functional role of both H1 and H2 receptors in the various guinea-pig heart sections.

摘要

研究了2-吡啶乙胺(PEA)和4-甲基组胺(4MeH)对豚鼠心脏不同部位的机械和电生理效应。4MeH使右心室和右心房的收缩力呈剂量依赖性增加,并使所有研究部位的功能不应期(FRP)缩短;心房和心室的动作电位时程均缩短,平台期通常升高。这些效应均被西咪替丁持续拮抗。在西咪替丁存在的情况下,研究了PEA引起的收缩力、FRP和动作电位形态的变化。曲普利啶仅在左心房拮抗PEA对FRP和动作电位形态的作用。根据H1和H2受体在豚鼠心脏不同部位的功能作用对所得结果进行了讨论。

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