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硝基血管扩张剂。关于老药的新观点。

The nitrovasodilators. New ideas about old drugs.

作者信息

Harrison D G, Bates J N

机构信息

Department of Internal Medicine, Emory University School of Medicine, Atlanta, GA 30322.

出版信息

Circulation. 1993 May;87(5):1461-7. doi: 10.1161/01.cir.87.5.1461.

Abstract

The nitrovasodilators are a diverse group of pharmacological agents that produce vascular relaxation by releasing nitric oxide. The mechanisms by which these compounds release nitric oxide vary, depending on their chemical structure. Compounds with lower oxidation states of nitrogen such as nitroprusside, nitrosamines, and nitrosothiols release nitric oxide nonenzymatically. In the case of nitroprusside, this involves a one-electron reduction that may occur upon exposure to a variety of reducing agents and tissues such as vascular smooth muscle membranes. In the case of the organic nitrates, which have higher oxidation states of nitrogen, the release of nitric oxide in vascular tissue occurs predominantly by a poorly understood enzymatic process. This interesting property of nitroglycerin is important because it "targets" its effect to vascular tissues that are capable of this enzymatic process. In the case of the coronary circulation, nitroglycerin predominantly dilates the larger coronary arteries while having a minimal effect on coronary resistance vessels < 100 microns in diameter. This prevents the development of coronary steal, which is often encountered with agents that produce intense vasodilation of the coronary resistance vessels. In this review, the mechanisms by which the nitrovasodilators (particularly nitroglycerin) release nitric oxide will be considered, and recent studies of nitroglycerin bioconversion in various-sized coronary vessels will be discussed in detail.

摘要

硝基血管扩张剂是一类多样的药理剂,它们通过释放一氧化氮来产生血管舒张作用。这些化合物释放一氧化氮的机制各不相同,取决于它们的化学结构。氮氧化态较低的化合物,如硝普钠、亚硝胺和亚硝基硫醇,非酶促释放一氧化氮。就硝普钠而言,这涉及单电子还原,可能在暴露于多种还原剂和组织(如血管平滑肌膜)时发生。对于氮氧化态较高的有机硝酸盐,血管组织中一氧化氮的释放主要通过一个了解甚少的酶促过程发生。硝酸甘油的这一有趣特性很重要,因为它将其作用“靶向”到能够进行这种酶促过程的血管组织。在冠状动脉循环中,硝酸甘油主要扩张较大的冠状动脉,而对直径小于100微米的冠状动脉阻力血管影响极小。这可防止出现冠状动脉窃血现象,而这种现象在能使冠状动脉阻力血管产生强烈血管舒张作用的药物中经常出现。在本综述中,将探讨硝基血管扩张剂(特别是硝酸甘油)释放一氧化氮的机制,并详细讨论硝酸甘油在各种大小冠状动脉血管中的生物转化的最新研究。

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