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钙离子载体A23187(钙霉素)对豚鼠心房的正性肌力和变时作用。

Positive inotropic and chronotropic effects of the calcium ionophore A23187 (calimycin) on guinea-pig atria.

作者信息

Himmel H M, Siess M

机构信息

Department of Pharmacology, University of Tübingen, F.R.G.

出版信息

Basic Res Cardiol. 1988 Mar-Apr;83(2):167-75. doi: 10.1007/BF01907271.

Abstract

The inotropic and chronotropic effects of the calcium ionophore A23187 (calimycin = CA) in isolated, superfused, electrically driven, auxotonically contracting left and spontaneously beating right guinea-pig atria were examined at different Ca2+ concentrations. 10(-6) to 10(-5) mol/l CA shows significantly positive inotropic and chronotropic effects. The inotropic effect of CA can be significantly diminished by relatively high concentrations of Ca2+ channel antagonists and relatively low concentrations of ryanodine. The positive chronotropic effect of CA can be reduced slightly, but significantly, by beta-adrenoceptor antagonists and histamine H2-receptor antagonists. From this we infer that the positive inotropic effect of CA is mainly due to the release of Ca2+ from cardiac sarcoplasmic reticulum, whereas catecholamine and histamine release appear to contribute to the positive chronotropic effect of the ionophore.

摘要

在不同钙离子浓度下,研究了钙离子载体A23187(钙霉素=CA)对分离的、经超灌流、电驱动、等长收缩的豚鼠左心房以及自发搏动的右心房的变力性和变时性作用。10(-6)至10(-5)mol/l的CA显示出显著的正性变力性和变时性作用。相对高浓度的钙通道拮抗剂和相对低浓度的ryanodine可显著减弱CA的变力性作用。β-肾上腺素能受体拮抗剂和组胺H2受体拮抗剂可使CA的正性变时性作用略有但显著降低。由此我们推断,CA的正性变力性作用主要是由于心肌肌浆网释放钙离子,而儿茶酚胺和组胺释放似乎对离子载体的正性变时性作用有贡献。

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