组胺H1和H2受体在犬肾中的作用。

Renal physiology Pub Date : 1985-01-01 DOI:10.1159/000173041
K J Radke, E E Selkurt, L R Willis
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引用次数: 14

摘要

研究了H1和H2受体介导组胺对麻醉犬肾血流动力学和肾小管功能的影响。组胺直接输注肾动脉后,肾血管阻力降低,肾总血流量增加,平均动脉血压和肾小球滤过率均无明显变化。组胺的这些血流动力学作用可被h2受体拮抗剂西咪替丁抑制,但不能被h1受体拮抗剂三烯胺抑制。组胺也引起尿流量增加,钠和钙的排泄增加,同时尿/血浆渗透压降低。三烯胺和西咪替丁均可拮抗组胺的这些管状作用。组胺引起的钾的部分排泄增加仅被三烯胺阻断。以上结果表明:(1)H1和H2受体均介导组胺对尿稀释和肾小管重吸收的影响;(2) H2受体介导组胺对肾血流动力学的影响,表明H2受体存在于肾血管中;(3)H1受体可能存在于肾小管中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The role of histamine H1 and H2 receptors in the canine kidney.

The functional role of H1 and H2 receptors in mediating the effects of histamine on renal hemodynamics and tubular function was investigated in anesthetized dogs. Histamine, infused directly into the renal artery, caused decreases in renal vascular resistance and increases in total renal blood flow without significant changes in mean arterial blood pressure or glomerular filtration rate. These hemodynamic effects of histamine were inhibited by the H2-receptor antagonist, cimetidine, but not by the H1-receptor antagonist, tripelennamine. Histamine also caused increases in fractional urine flow and the fractional excretion of sodium and calcium with a concomitant decrease in urine/plasma osmolality. These tubular effects of histamine were antagonized by both tripelennamine and cimetidine. Histamine-induced increases in the fractional excretion of potassium were blocked only by tripelennamine. These results suggest that (1) both H1 and H2 receptors mediate the effects of histamine on urinary dilution and tubular reabsorption; (2) H2 receptors mediate the effects of histamine on renal hemodynamics, indicating that H2 receptors are present in the renal vasculature, and (3) H1 receptors may exist in the renal tubules.

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