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兔心房中H和H2组胺受体的证据。

Evidence for both H and H2-histamine receptors in rabbit atria.

作者信息

Srivastava R D

出版信息

Indian J Physiol Pharmacol. 1980 Jan-Mar;24(1):37-42.

PMID:7364459
Abstract

Spontaneously beating isolated atria of rabbits responded to histamine (0.5-16 micrograms/ml) with positive chrono- and inotropism. However, the inotropic response was greater than chronotropic one. The concentration-response curve of histamine for chronotropic effect was markedly shifted to the right in the presence of 0.5 micrograms/ml metiamide (H2-receptor antagonist), which per se augmented the control contractile amplitude in all the experiments. The rightward shift of chronotropic concentration response curve with mepyramine (H1-antagonist) was, however, moderate. On the contrary, the inotropic concentration response curve of histamine was shifted to much greater extent to right with mepyramine (0.62 micrograms/ml) than with metiamide, thus suggesting a greater share of H1 than H2-receptors in the mediation of positive inotropic effect of histamine. The chronotropic effect appears to be mediated predominently by H2-receptors. Unlike metiamide, mepyramine did not alter the spontaneous frequency or amplitude of contraction. The present study, thus lends support for dual histamine receptors in rabbit atria.

摘要

家兔离体自发搏动心房对组胺(0.5 - 16微克/毫升)呈现正性变时和变力作用。然而,变力反应大于变时反应。在存在0.5微克/毫升甲硫米特(H2受体拮抗剂)时,组胺变时效应的浓度 - 反应曲线显著右移,而甲硫米特本身在所有实验中均增加了对照收缩幅度。用美吡拉敏(H1拮抗剂)时,变时浓度反应曲线的右移则较为适度。相反,组胺的变力浓度反应曲线在使用美吡拉敏(0.62微克/毫升)时比使用甲硫米特时右移程度更大,这表明在组胺正性变力作用的介导中,H1受体比H2受体起更大作用。变时效应似乎主要由H2受体介导。与甲硫米特不同,美吡拉敏不改变自发频率或收缩幅度。因此,本研究支持家兔心房中存在双重组胺受体。

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