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克罗卡林与吡那地尔对犬冠状动脉机械活性及⁸⁶Rb外流影响的比较。

Comparison of effects of cromakalim and pinacidil on mechanical activity and 86Rb efflux in dog coronary arteries.

作者信息

Masuzawa K, Asano M, Matsuda T, Imaizumi Y, Watanabe M

机构信息

Department of Pharmacology, Nagoya City University Medical School, Japan.

出版信息

J Pharmacol Exp Ther. 1990 May;253(2):586-93.

PMID:2160002
Abstract

Effects of two K+ channel openers, cromakalim and pinacidil, on mechanical activity and on 86Rb efflux were compared in strips of dog coronary arteries. Cromakalim and pinacidil produced the relaxation in 20.9 mM K(+)-contracted strips with a pD2 of 6.53 and 5.95, respectively. In 65.9 mM K(+)-contracted strips, high concentrations of pinacidil, but not cromakalim, produced relaxation. Ca+(+)-induced contractions in 80 mM K(+)-depolarized strips were also inhibited by pinacidil but not by cromakalim. Glibenclamide, a blocker of ATP-regulated K+ (KATP) channels, competitively antagonized the relaxant responses to cromakalim with a pA2 value of 7.62. However, the antagonism by glibenclamide of the relaxant responses to pinacidil was not a typical competitive type, suggesting the contribution of other effects than the KATP channel opening activity to the relaxant effects of pinacidil. In resting strips preloaded with 86Rb, cromakalim and pinacidil increased the basal 86Rb efflux in a dose-dependent manner. The increase in the 86Rb efflux induced by cromakalim was greater than that by pinacidil. When the effects of cromakalim and pinacidil on the 86Rb efflux were determined in the 20.9 or 65.9 mM K(+)-contracted strips, both drugs increased the 86Rb efflux. Under the same conditions nifedipine, a Ca(+)+ channel blocker, produced the relaxation that is accompanied by the decrease in 86Rb efflux. The increase in the 86Rb efflux induced by cromakalim was much greater than that by pinacidil.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在犬冠状动脉条上比较了两种钾通道开放剂——克罗卡林和吡那地尔对机械活性及86Rb外流的影响。克罗卡林和吡那地尔使20.9 mM K⁺收缩条产生松弛,其pD2分别为6.53和5.95。在65.9 mM K⁺收缩条中,高浓度的吡那地尔可产生松弛,而克罗卡林则不能。80 mM K⁺去极化条中Ca²⁺诱导的收缩也被吡那地尔抑制,但未被克罗卡林抑制。格列本脲是ATP调节钾(KATP)通道的阻滞剂,以pA2值7.62竞争性拮抗对克罗卡林的松弛反应。然而,格列本脲对吡那地尔松弛反应的拮抗并非典型的竞争类型,提示除KATP通道开放活性外,其他效应也参与了吡那地尔的松弛作用。在预先加载86Rb的静息条中,克罗卡林和吡那地尔以剂量依赖性方式增加基础86Rb外流。克罗卡林诱导的86Rb外流增加大于吡那地尔。当在20.9或65.9 mM K⁺收缩条中测定克罗卡林和吡那地尔对86Rb外流的影响时,两种药物均增加86Rb外流。在相同条件下,钙通道阻滞剂硝苯地平产生松弛并伴有86Rb外流减少。克罗卡林诱导的86Rb外流增加远大于吡那地尔。(摘要截断于250字)

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