Radke K J, Selkurt E E, Willis L R
Ren Physiol. 1985;8(2):100-11. doi: 10.1159/000173041.
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.
在麻醉犬身上研究了H1和H2受体在介导组胺对肾血流动力学和肾小管功能影响中的作用。将组胺直接注入肾动脉,可导致肾血管阻力降低、肾总血流量增加,而平均动脉血压或肾小球滤过率无显著变化。组胺的这些血流动力学效应被H2受体拮抗剂西咪替丁抑制,但未被H1受体拮抗剂曲吡那敏抑制。组胺还导致尿流分数以及钠和钙的排泄分数增加,同时尿/血浆渗透压降低。组胺的这些肾小管效应被曲吡那敏和西咪替丁两者拮抗。组胺诱导的钾排泄分数增加仅被曲吡那敏阻断。这些结果表明:(1)H1和H2受体均介导组胺对尿液稀释和肾小管重吸收的作用;(2)H2受体介导组胺对肾血流动力学的作用,表明肾血管系统中存在H2受体;(3)H1受体可能存在于肾小管中。