组胺和抗组胺药对大鼠体内二氧化碳动力学的影响。

Physiological chemistry and physics Pub Date : 1981-01-01
J C Russell, M M Chambers
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引用次数: 0

摘要

我们研究了chlorpheniramine(一种H1组胺抑制剂)和metiamide(一种H2抑制剂)在存在和不存在组胺的情况下对大鼠二氧化碳14C脉冲标记反应的影响。单独使用氯苯那敏或甲氨酰胺对胃静脉/动脉比值(VG/A)或外周静脉/动脉比值(Vp/A)均无影响。与没有药物存在的情况一样,在脉冲标记后,Vp/A随着时间的推移而上升,达到1.15-1.20。在存在或不存在抑制剂的情况下,预先存在的稳定状态组胺输注的存在不会引起比例的变化。抑制剂确实完全消除了与脉冲标记一致的组胺输注起始引起的VG/A和Vp/A的振荡。结果表明组胺的作用主要是通过H1受体介导的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of histamine and antihistamines on the kinetics of carbon dioxide in the rat.

We have investigated the effects of chlorpheniramine (an H1 histamine inhibitor) and metiamide (an H2 inhibitor) on response to 14C pulse-labeling of carbon dioxide in the rat in the presence and absence of histamine. Neither chlorpheniramine nor metiamide alone had any effect upon the gastric venous/arterial ratio (VG/A) or the peripheral venous/arterial ratio (Vp/A). As in the case with no drug present, Vp/A rose with time following pulse-labeling to a value of 1.15-1.20. The presence of a preexisting steady-state infusion of histamine caused no changes in the ratios in the presence or absence of the inhibitors. The inhibitors did completely abolish the oscillations of both VG/A and Vp/A caused by initiation of histamine infusion coincident with the pulse-labeling. The results suggest that the histamine effects are largely mediated through H1 receptors.

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