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5-羟色胺1受体介导的牛离体肺动脉血管收缩:血管内皮及张力的影响

5-HT1-receptor-mediated vasoconstriction in bovine isolated pulmonary arteries: influences of vascular endothelium and tone.

作者信息

MacLean M R, Clayton R A, Hillis S W, McIntyre P D, Peacock A J, Templeton A G

机构信息

Institute of Physiology, University of Glasgow, UK.

出版信息

Pulm Pharmacol. 1994 Feb;7(1):65-72. doi: 10.1006/pulp.1994.1007.

Abstract

Vasoconstrictor responses to 5-hydroxytryptamine (5-HT) and the 5-HT1D receptor agonist sumatriptan were studied in isolated bovine pulmonary artery rings. The effects of the antagonists, ketanserin (5-HT2A-receptors) and methiothepin (5-HT1- and 5-HT2A-receptors) on these responses were determined. The influences of vascular tone and the effect of removal of the vascular endothelium and pretreatment with the inhibitor of nitric oxide synthase, N omega-nitro-L-arginine methylester, were also studied. In the absence of tone, in the majority of vessels, sumatriptan did not induce significant contractions. 5-HT-induced responses were concentration-dependent and ketanserin and methiothepin antagonized these in a competitive fashion. Removal of the endothelium or inclusion of L-NAME potentiated responses to sumatriptan. The sensitivity to sumatriptan was increased by L-NAME only in the presence of the endothelium whilst maximum responses to sumatriptan were potentiated in both unrubbed and rubbed vessels. Removal of the endothelium and/or inclusion of L-NAME had no significant effect on responses to 5-HT. U46619-induced tone markedly increased sumatriptan-induced responses which were competitively antagonized by methiothepin but were relatively resistant to ketanserin, verifying activation of a 5-HT1D receptor. Responses to 5-HT were also potentiated and competitively antagonized by ketanserin, and further antagonized by methiothepin. With tone present, lower concentrations of 5-HT were ketanserin-resistant and methiothepin-sensitive, indicating activation of a 5-HT1-like receptor.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在离体牛肺动脉环中研究了对5-羟色胺(5-HT)和5-HT1D受体激动剂舒马曲坦的血管收缩反应。测定了拮抗剂酮色林(5-HT2A受体)和甲硫噻平(5-HT1和5-HT2A受体)对这些反应的影响。还研究了血管张力的影响、去除血管内皮的作用以及用一氧化氮合酶抑制剂Nω-硝基-L-精氨酸甲酯预处理的效果。在无张力状态下,在大多数血管中,舒马曲坦未引起明显收缩。5-HT诱导的反应呈浓度依赖性,酮色林和甲硫噻平以竞争性方式拮抗这些反应。去除内皮或加入L-NAME可增强对舒马曲坦的反应。仅在内皮存在时,L-NAME可增加对舒马曲坦的敏感性,而在未摩擦和摩擦的血管中,对舒马曲坦的最大反应均增强。去除内皮和/或加入L-NAME对5-HT诱导的反应无显著影响。U46619诱导的张力显著增加舒马曲坦诱导的反应,这些反应被甲硫噻平竞争性拮抗,但对酮色林相对耐药,证实了5-HT1D受体的激活。对5-HT的反应也被酮色林增强并竞争性拮抗,进一步被甲硫噻平拮抗。在有张力的情况下,较低浓度的5-HT对酮色林耐药而对甲硫噻平敏感,表明激活了一种5-HT1样受体。(摘要截短于250字)

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