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肽类和非肽类对离体动脉平滑肌的作用:内皮的作用

Effects of peptides and non-peptides on isolated arterial smooth muscles: role of endothelium.

作者信息

D'Orléans-Juste P, Dion S, Mizrahi J, Regoli D

出版信息

Eur J Pharmacol. 1985 Aug 7;114(1):9-21. doi: 10.1016/0014-2999(85)90515-1.

Abstract

Peptides and non-peptides acting as vasoconstrictors or vasodilators have been tested in dog isolated carotid arteries with and without endothelium and in the presence and absence of a variety of antagonists and inhibitors of endogenous substances. It has been found that substance P and several other tachykinins, bradykinin, neurotensin, bombesin and acetylcholine relax the isolated artery only when the endothelium is present, while VIP, isopropylnoradrenaline, adenosine, histamine, prostaglandins E1 and E2, glucagon and insulin relax and angiotensin, vasopressin, oxytocin, 5-HT and noradrenaline contract the isolated vessel, no matter whether the endothelium is present or not. Peptide and non-peptide antagonists have been used with success to show that vasoconstrictors and vasodilators act on specific receptors, since their effects are reduced in the presence of antagonists, specific for one or another of the various agents. Inhibitors of the arachidonic acid cascade only reduce the effect of acetylcholine, suggesting that at least two different mechanisms are involved in the endothelium-mediated relaxation of arterial smooth muscles to peptide and non-peptide agents. The results summarised in this paper suggest that the site of action of several vasodilators is the endothelium, while other vasodilators and all the vasoconstrictors influence the arterial vessels tone presumably by acting on the smooth muscle cells.

摘要

作为血管收缩剂或血管舒张剂的肽类和非肽类物质,已在有内皮和无内皮的犬离体颈动脉中进行了测试,且测试是在存在和不存在多种内源性物质拮抗剂和抑制剂的情况下进行的。已发现,只有在内皮存在时,P物质和其他几种速激肽、缓激肽、神经降压素、蛙皮素和乙酰胆碱才能使离体动脉舒张,而血管活性肠肽、异丙去甲肾上腺素、腺苷、组胺、前列腺素E1和E2、胰高血糖素和胰岛素则能使离体血管舒张,血管紧张素、血管加压素、催产素、5-羟色胺和去甲肾上腺素则能使离体血管收缩,无论内皮是否存在。肽类和非肽类拮抗剂已成功用于表明血管收缩剂和血管舒张剂作用于特定受体,因为在存在针对各种药物中某一种的拮抗剂时,它们的作用会减弱。花生四烯酸级联反应的抑制剂仅能降低乙酰胆碱的作用,这表明动脉平滑肌对肽类和非肽类药物的内皮介导舒张至少涉及两种不同机制。本文总结的结果表明,几种血管舒张剂的作用部位是内皮,而其他血管舒张剂和所有血管收缩剂可能是通过作用于平滑肌细胞来影响动脉血管张力。

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