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大鼠血管组胺受体的特性研究

Characterization of vascular histamine receptors in the rat.

作者信息

Powell J R, Shamel L B

出版信息

Br J Pharmacol. 1979 Aug;66(4):517-20. doi: 10.1111/j.1476-5381.1979.tb13688.x.

Abstract

1 In the rat the decrease in blood pressure caused by histamine involves activation of both H1- and H2-receptors. Since arterial pressure measurements alone do not permit the separation of responses into cardiac and vascular components, the following experiments were undertaken to study vascular histamine receptors. 2 Vascular responses were studied in the autoperfused hindquarters of anaesthetized rats. Intra-arterial histamine caused vasodilatation which was only partially attenuated by treatment with mepyramine, an H1-receptor antagonist. Treatment with metiamide, the H2-receptor antagonist, did not affect vasodilatation caused by histamine but did attenuate vasodilatation which persisted after mepyramine. 3 Intra-arterial 4-methylhistamine, an H2-receptor agonist, caused vasodilatation which was reduced by metiamide. The H1-receptor agonist, 2-(2-pyridyl)ethylamine also caused vasodilatation which was blocked by mepyramine. 4 It is concluded that in the rat, histamine causes vasodilatation mediated by both H1- and H2-receptors.

摘要
  1. 在大鼠中,组胺引起的血压下降涉及H1和H2受体的激活。由于仅通过测量动脉血压无法将反应区分为心脏和血管成分,因此进行了以下实验以研究血管组胺受体。2. 在麻醉大鼠的自体灌注后肢中研究血管反应。动脉内注射组胺引起血管舒张,用H1受体拮抗剂美吡拉敏治疗只能部分减弱这种舒张。用H2受体拮抗剂甲硫米特治疗并不影响组胺引起的血管舒张,但确实减弱了美吡拉敏治疗后持续存在的血管舒张。3. 动脉内注射H2受体激动剂4-甲基组胺引起血管舒张,甲硫米特可使其减弱。H1受体激动剂2-(2-吡啶基)乙胺也引起血管舒张,美吡拉敏可阻断这种舒张。4.得出结论,在大鼠中,组胺通过H1和H2受体介导引起血管舒张。

相似文献

1
Characterization of vascular histamine receptors in the rat.大鼠血管组胺受体的特性研究
Br J Pharmacol. 1979 Aug;66(4):517-20. doi: 10.1111/j.1476-5381.1979.tb13688.x.
8
Histamine H1- and H2-receptors in the gastrointestinal circulation.胃肠道循环中的组胺H1和H2受体。
Naunyn Schmiedebergs Arch Pharmacol. 1980 Jun;312(2):123-9. doi: 10.1007/BF00569720.

本文引用的文献

2
Receptors mediating some actions of histamine.介导组胺某些作用的受体。
Br J Pharmacol Chemother. 1966 Aug;27(2):427-39. doi: 10.1111/j.1476-5381.1966.tb01674.x.

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