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猫和大鼠肠系膜循环中的组胺受体。

Histamine receptors in mesenteric circulation of the cat and rat.

作者信息

Guth P H, Smith E

出版信息

Am J Physiol. 1978 Apr;234(4):E370-4. doi: 10.1152/ajpendo.1978.234.4.E370.

Abstract

This study was designed to ascertain the types and functions of histamine receptors in the mesenteric circulation of the cat and rat. Superior mesenteric artery (SMA) flow was measured via an electromagnetic probe in the cat and intestinal submucosal arteriolar diameter by an image-splitting in vivo microscopy technique in the cat and rat. Histamine infusion into the SMA caused dose-dependent decreases in mesenteric vascular resistance. Mepyramine, an H1 receptor antagonist (H1A), inhibited this effect, displacing the histamine dose-response curve to the right. Metiamide, an H2 receptor antagonist (H2A), alone had no effect, but in the presence of H1A caused further displacement of the curve to the right. In both the cat and the rat, histamine superfusion dilated the submucosal arterioles. H1A attenuated this effect. H2A alone had no effect, but in the presence of H1A there was nearly complete inhibition of the histamine effect. In conclusion, both H1 and H2 histamine receptors, both subserving vasodilatation, are present in the mesenteric circulation and the H1 receptor effect predominates.

摘要

本研究旨在确定猫和大鼠肠系膜循环中组胺受体的类型和功能。通过电磁探头测量猫的肠系膜上动脉(SMA)血流量,并利用图像分割活体显微镜技术测量猫和大鼠的肠黏膜下小动脉直径。向SMA内注入组胺可引起肠系膜血管阻力呈剂量依赖性降低。H1受体拮抗剂(H1A)美吡拉敏可抑制这种效应,使组胺剂量反应曲线右移。H2受体拮抗剂(H2A)甲硫咪特单独使用无作用,但在存在H1A时可使曲线进一步右移。在猫和大鼠中,组胺灌流均可使黏膜下小动脉扩张。H1A可减弱这种效应。H2A单独使用无作用,但在存在H1A时,组胺效应几乎完全被抑制。总之,肠系膜循环中同时存在H1和H2组胺受体,二者均参与血管舒张,且H1受体效应占主导。

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