Cocaine-induced hypertension: Role of the peripheral sympathetic system

被引:15
作者
Mo, W
Arruda, JAL
Dunea, G
Singh, AK
机构
[1] Hektoen Inst Med Res, Chicago, IL 60612 USA
[2] Cook Cty Hosp, Div Nephrol, Chicago, IL 60612 USA
[3] Univ Illinois, Nephrol Sect, Chicago, IL 60612 USA
关键词
cocaine; hypertension; vasoconstriction; norepinephrine; prazosin; clonidine;
D O I
10.1006/phrs.1999.0503
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cocaine causes hypertension at least in part by stimulating the sympathetic nervous system, but it is not clear if this effect is centrally or peripherally mediated. To address this issue we studied the vasoconstrictive effect of cocaine in vivo and in isolated artery segments. In vivo cocaine increased mean arterial blood pressure (MAP) by 40 mmHg within 1 min of administration. Pretreatment with prazosin blocked this response by 62%. With clonidine the pre-cocaine MAP was lower and the hypertensive effect of cocaine was blocked by 50%, indicating an important role for central alpha-adrenergic mechanisms. In isolated rat carotid arteries cocaine-induced vasoconstriction was completely blocked by prazosin, phentolamine, and 6-hydroxydopamine, indicating a clear role for a peripheral effect. However, the relative contribution of the central alpha-adrenergic mechanism to the total vasoconstrictive response of cocaine was not clarified. (C) 1999 Academic Press.
引用
收藏
页码:139 / 145
页数:7
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