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内源性阿片类物质与高血压的发病机制

Endogenous opiates and the pathogenesis of hypertension.

作者信息

Szilagyi J E

机构信息

Department of Pharmacology, University of Houston, Texas 77204-5515.

出版信息

Clin Exp Hypertens A. 1989;11(1):1-24. doi: 10.3109/10641968909035287.

Abstract

Opiates are now known to be important modulators of cardiovascular function in both the normotensive and hypertensive states. There is accumulating evidence that endogenous opiates are elevated in models of hypertension of various etiologies including genetic and renovascular hypertension. Early evidence for elevated opiates in hypertension arose from observations that hypertensive humans and rats with genetic or experimental hypertension exhibited hypoalgesia in various tests of pain sensitivity. Because pain and cardiovascular regulatory systems have in common a number of brain loci, cardiovascular effects of opiates and opiate blockade were studied. These studies have shown that opiate blockade can attenuate the development of hypertension and reduce blood pressure in chronic hypertension possibly via actions on the baroreflexes and/or by modulating the centrally mediated pressor actions of angiotensin II.

摘要

目前已知阿片类药物在正常血压和高血压状态下都是心血管功能的重要调节因子。越来越多的证据表明,在包括遗传性高血压和肾血管性高血压在内的各种病因所致的高血压模型中,内源性阿片类物质水平升高。高血压患者以及患有遗传性或实验性高血压的大鼠在各种疼痛敏感性测试中表现出痛觉减退,由此得出了高血压患者体内阿片类物质水平升高的早期证据。由于疼痛和心血管调节系统在许多脑区存在共同之处,因此对阿片类药物及其阻断作用的心血管效应进行了研究。这些研究表明,阿片类药物阻断可能通过作用于压力感受器反射和/或调节血管紧张素II的中枢介导升压作用,来减弱高血压的发展并降低慢性高血压患者的血压。

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