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组胺对人离体肺动脉和静脉作用的研究。

Studies on the effect of histamine in isolated human pulmonary arteries and veins.

作者信息

Mikkelsen E, Sakr A M, Jespersen L T

出版信息

Acta Pharmacol Toxicol (Copenh). 1984 Feb;54(2):86-93. doi: 10.1111/j.1600-0773.1984.tb01900.x.

Abstract

The effect of histamine (0.01-200 microM) was studied in isolated human pulmonary vessels. Histamine induced concentration dependent contractions in both arteries and veins. In veins the maximal response to histamine was lower than in arteries. Histamine and 2-methyl-histamine had a dual action in both arteries and veins clearly demonstrated in vessels precontracted with potassium. In these vessels histamine and 2-methyl-histamine induced relaxation at low concentrations and contractions at high concentrations. Veins were more sensitive to the relaxant effect of histamine than arteries. Mepyramine eliminated the dual action of 2-methyl-histamine and histamine and unveiled a mepyramine resistant relaxation at the highest histamine concentrations used which was resistant to the effect of cimetidine and metiamide. The H2 receptor agonist dimaprit (10-400 microM) induced a slight relaxation in both arteries and veins that could be eliminated by metiamide (100 microM). The results show that histamine has a dual action in human pulmonary vessels which includes a contractile effect mediated via H1 receptors and a relaxant response partly mediated through H1 receptors and partly via unspecific mechanisms. However, an H2 mediated relaxant effect cannot be excluded.

摘要

在离体的人肺血管中研究了组胺(0.01 - 200微摩尔)的作用。组胺在动脉和静脉中均诱导浓度依赖性收缩。在静脉中,对组胺的最大反应低于动脉。组胺和2 - 甲基组胺在动脉和静脉中均有双重作用,这在预先用钾收缩的血管中得到了明确证明。在这些血管中,组胺和2 - 甲基组胺在低浓度时诱导舒张,在高浓度时诱导收缩。静脉对组胺的舒张作用比动脉更敏感。美吡拉敏消除了2 - 甲基组胺和组胺的双重作用,并在所用的最高组胺浓度下揭示了一种对西咪替丁和甲硫米特作用有抗性的美吡拉敏抗性舒张。H2受体激动剂二甲双胍(10 - 400微摩尔)在动脉和静脉中均诱导轻微舒张,这种舒张可被甲硫米特(100微摩尔)消除。结果表明,组胺在人肺血管中具有双重作用,包括通过H1受体介导的收缩作用和部分通过H1受体以及部分通过非特异性机制介导的舒张反应。然而,不能排除H2介导的舒张作用。

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