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在正常血压和高血压老龄大鼠的血管中,缓激肽诱导的血管舒张转变为血管收缩反应。

Bradykinin-induced vasodilation is changed to a vasoconstrictor response in vessels of aged normotensive and hypertensive rats.

作者信息

Mantelli L, Amerini S, Ledda F

机构信息

Department of Pharmacology, University of Florence, Italy.

出版信息

Inflamm Res. 1995 Feb;44(2):70-3. doi: 10.1007/BF01793215.

Abstract

The vascular response to bradykinin was investigated in mesenteric vascular bed preparations preconstricted with methoxamine, obtained from 2- and 18-month old normotensive (WKY) and spontaneously hypertensive (SHR) rats. In preparations from young normotensive rats bradykinin (1 nm-10 microM) produced an endothelium-dependent vasorelaxant effect which was greatly reduced by the B2 receptor antagonist Ac-D-Arg[Hyp3,D-Phe7,Leu8]-bradykinin (1 microM), and was unaffected by the B1 receptor antagonist des-Arg9,[Leu8]-bradykinin (1 microM). The degree of vasodilation was similar in preparations from age-matched SHR rats. In vessels obtained from old animals bradykinin induced an endothelium-independent vasoconstrictor response; this effect was more pronounced in preparations from SHR than in those from WKY rats. The vasoconstriction was unaffected by both B1 and B2 receptor antagonists, and was abolished by 3 microM indomethacin. We conclude that the vasorelaxant effect of bradykinin in vessels of young animals is due to stimulation of B2 receptors. This vasodilating response can be converted by aging to a vasoconstriction and is probably due to the release of a prostanoid product; moreover it is more pronounced in spontaneously hypertensive animals.

摘要

在从2月龄和18月龄正常血压(WKY)大鼠及自发性高血压(SHR)大鼠获取的、用甲氧明预收缩的肠系膜血管床制备物中,研究了血管对缓激肽的反应。在年轻正常血压大鼠的制备物中,缓激肽(1 nM - 10 μM)产生内皮依赖性血管舒张作用,该作用被B2受体拮抗剂Ac-D-Arg[Hyp3,D-Phe7,Leu8]-缓激肽(1 μM)显著减弱,且不受B1受体拮抗剂去-Arg9,[Leu8]-缓激肽(1 μM)影响。年龄匹配的SHR大鼠制备物中的血管舒张程度相似。在老年动物获取的血管中,缓激肽诱导内皮非依赖性血管收缩反应;该效应在SHR大鼠的制备物中比在WKY大鼠的制备物中更明显。血管收缩不受B1和B2受体拮抗剂影响,且被3 μM吲哚美辛消除。我们得出结论,缓激肽在年轻动物血管中的血管舒张作用是由于B2受体的刺激。这种血管舒张反应可因衰老转变为血管收缩,可能是由于一种前列腺素产物的释放;此外,在自发性高血压动物中更明显。

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