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H1和H2组胺受体在生理性血管舒张反应中的作用。

Participation of H1 and H2 histamine receptors in physiological vasodilator responses.

作者信息

Powell J R, Brody M J

出版信息

Am J Physiol. 1976 Oct;231(4):1002-9. doi: 10.1152/ajplegacy.1976.231.4.1002.

Abstract

Histamine causes vasodilation in the dog by activation of H1 and H2 receptors blocked by mepyramine and metiamide, respectively. Experiments were conducted in anesthetized dogs to determine the participation of H1 and H2 receptors in several forms of physiological dilatation. Mepyramine attenuated both histamine-induced and active-reflex dilatation in the hindlimb. Metiamide caused a further reduction in both sets of dilatation. Neither single nor combined antihistamines reduced dilatation due to exercise or after temporary occlusion of the circulation in the hindlimb. Poststimulation dilatation in the gracilis muscle was partially attenuated by metiamide or mepyramine. Neither dilatation caused by sympathetic nerve stimulation in the hindpaw nor dilatation in the gracilis muscle caused by compound 48/80 was reduced by mepyramine. Following combined H1- and H2-receptor blockade, portions of both types of dilatation were reduced. These data provide evidence for the participation of both types of histamine receptor in active reflex dilatation, low-frequency neurogenic dilatation, dilatation caused by compound 48/80, and poststimulation dilatation. Neither type of histamine receptor appears to be involved in reactive hyperemia or dilatation caused by exercise.

摘要

组胺通过激活分别被美吡拉敏和甲硫咪特阻断的H1和H2受体,引起犬的血管舒张。在麻醉犬身上进行了实验,以确定H1和H2受体在几种生理性扩张形式中的参与情况。美吡拉敏减弱了组胺诱导的和后肢主动反射性扩张。甲硫咪特使这两种扩张进一步减弱。无论是单独使用还是联合使用抗组胺药,都不能减轻运动或后肢循环暂时阻断后引起的扩张。甲硫咪特或美吡拉敏使股薄肌刺激后扩张部分减弱。美吡拉敏不能减轻后爪交感神经刺激引起的扩张,也不能减轻48/80化合物引起的股薄肌扩张。联合阻断H1和H2受体后,两种类型的扩张部分都有所减少。这些数据为两种类型的组胺受体参与主动反射性扩张、低频神经源性扩张、48/80化合物引起的扩张和刺激后扩张提供了证据。两种类型的组胺受体似乎都不参与运动引起的反应性充血或扩张。

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