Suppr超能文献

一条离体人体动脉的α-肾上腺素能受体反应与血压

Alpha-adrenoceptor responses of an isolated human artery and blood pressure.

作者信息

Wyse D G

机构信息

Department of Medicine (Cardiology), University of Calgary, Alta., Canada.

出版信息

J Vasc Res. 1995 Jan-Feb;32(1):66-78. doi: 10.1159/000159079.

Abstract

This cross-sectional study examined responses of the isolated cystic artery to 3 alpha-adrenoceptor agonists and the effects of 2 antagonists in relation to subjects' blood pressures. Potency of the 3 amines studied was: alpha-methylnorepinephrine > norepinephrine > phenylephrine. Responses to clonidine were trivial (< 5% of maximum) and remained < 25% of maximum in the presence of subthreshold concentrations of angiotensin II. A weak trend for increased potency of alpha-methylnorepinephrine was noted in arteries of subjects with higher blood pressures (r = 0.268, p = 0.027). There was no relationship between blood pressure and pA2 for yohimbine. The pA2 for prazosin could not be calculated because of a decline in maximal responses but prazosin was clearly more potent than yohimbine. The decline in maximal responses to norepinephrine and phenylephrine after prazosin treatment was related to subjects' diastolic blood pressures (r = -0.400, p = 0.003). There were no significant relationships between these measurements of vascular responsiveness and a family history of hypertension. There were also no significant relationships between these measurements of vascular responsiveness and plasma norepinephrine levels, alpha 2-adrenoceptor binding or platelets of beta 2-adrenoceptor binding of lymphocytes. The major postjunctional alpha-adrenoceptors in this artery are of the alpha 1 type. The data suggest that differences in potency of alpha-adrenoceptor agonists in relation to blood pressure may be due to differences in the alpha 2-adrenoceptor but are not likely due to a difference in binding to the receptor itself.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

这项横断面研究检测了孤立的胆囊动脉对3种α-肾上腺素能受体激动剂的反应以及2种拮抗剂在受试者血压方面的作用。所研究的3种胺类的效力为:α-甲基去甲肾上腺素>去甲肾上腺素>去氧肾上腺素。可乐定的反应很轻微(<最大反应的5%),在存在阈下浓度的血管紧张素II时,反应仍<最大反应的25%。在血压较高的受试者的动脉中,观察到α-甲基去甲肾上腺素效力增加的微弱趋势(r = 0.268,p = 0.027)。血压与育亨宾的pA2之间没有关系。由于最大反应下降,哌唑嗪的pA2无法计算,但哌唑嗪显然比育亨宾更有效。哌唑嗪治疗后去甲肾上腺素和去氧肾上腺素最大反应的下降与受试者的舒张压有关(r = -0.400,p = 0.003)。这些血管反应性测量值与高血压家族史之间没有显著关系。这些血管反应性测量值与血浆去甲肾上腺素水平、α2-肾上腺素能受体结合或淋巴细胞β2-肾上腺素能受体结合的血小板之间也没有显著关系。这条动脉中主要的节后α-肾上腺素能受体是α1型。数据表明,α-肾上腺素能受体激动剂效力与血压的差异可能归因于α2-肾上腺素能受体的差异,但不太可能是由于与受体本身结合的差异。(摘要截断于250字)

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验