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组胺H1和H2受体对犬肠道循环的血管舒张作用。

Histamine H1- and H2-receptor vasodilation of canine intestinal circulation.

作者信息

Pawlik W, Tague L L, Tepperman B L, Miller T A, Jacobson E D

出版信息

Am J Physiol. 1977 Sep;233(3):E219-24. doi: 10.1152/ajpendo.1977.233.3.E219.

Abstract

Studies were conducted in anesthetized dogs to determine whether the mesenteric vasodilator response to histamine is mediated by H1 receptors alone or whether H2 receptors are also involved in the response. Evidence favoring a role for both receptors included: 1) the vasodilator response to histamine was inhibited by either the H1-receptor antagonist, tripelennamine, or the H2-receptor antagonist, metiamide; 2) both the H1 agonist, 2-methylhistamine, and the H2 agonist, 4-methylhistamine, induced dilator responses in the mesenteric circulation; and 3) two temporal patterns of vasodilation could be distinguished, namely a transient spike and subsequent fade of blood flow (seen with either the H1 agonist or with histamine after H2-receptor blockade) and a sustained and stable increase in flow (seen with either the H2 agonist or with histamine after H1 blockade). Metiamide appeared to be a potent inhibitor of the mesenteric vasodilator response to histamine at least equal to tripelennamine.

摘要

在麻醉犬身上进行了多项研究,以确定肠系膜对组胺的血管舒张反应是否仅由H1受体介导,或者H2受体是否也参与了该反应。支持两种受体都起作用的证据包括:1)组胺的血管舒张反应可被H1受体拮抗剂曲吡那敏或H2受体拮抗剂甲硫米特抑制;2)H1激动剂2-甲基组胺和H2激动剂4-甲基组胺均可在肠系膜循环中诱导舒张反应;3)可以区分出两种血管舒张的时间模式,即血流的短暂峰值和随后的衰减(H2受体阻断后用H1激动剂或组胺可见)以及血流的持续稳定增加(H1阻断后用H2激动剂或组胺可见)。甲硫米特似乎是肠系膜对组胺血管舒张反应的一种有效抑制剂,其效力至少与曲吡那敏相当。

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