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丙泊酚对离体大鼠主动脉血管平滑肌功能的影响。

Effects of propofol on vascular smooth muscle function in isolated rat aorta.

作者信息

Mimaroglu C, Utkan T, Kaya T, Kafali H, Sarioglu Y

机构信息

Department of Anesthesiology, Cumhuriyet University, Sivas, Turkey.

出版信息

Methods Find Exp Clin Pharmacol. 1994 May;16(4):257-61.

PMID:8051985
Abstract

This study was undertaken to determine the direct actions of propofol, and whether propofol exerts any action on basal endothelium-derived relaxing factor release and vasodilator effect of acetylcholine on phenylephrine-induced contractile responses in isolated rat aortic rings. This compound is known to produce a fall in blood pressure in man and animals, and it has been suggested that the hypotension may result from a direct vasodilator action on the veins and arterioles. In this study, propofol did not induce any contractile response in aortic rings at various concentrations (10(-8)-10(-4) M). Propofol did not significantly alter phenylephrine-induced contractions at lower concentrations (10(-8)-10(-6) M) but at higher concentrations (10(-5)-10(-4) M) the depression caused by propofol was significant in both endothelium-intact and -denuded rings. Pretreatment of the endothelium-intact rings with propofol (10(-6) and 10(-5) M) produced a reduction in the relaxant effect of acetylcholine. The results obtained in this study demonstrate that clinically relevant concentrations of propofol (10(-6) M or less) have no direct vasodilator effects and that it reduces endothelium-dependent relaxation to acetylcholine.

摘要

本研究旨在确定丙泊酚的直接作用,以及丙泊酚是否对基础内皮衍生舒张因子的释放以及乙酰胆碱对苯肾上腺素诱导的离体大鼠主动脉环收缩反应的舒张作用产生影响。已知该化合物可使人和动物的血压下降,有人认为低血压可能是由于其对静脉和小动脉的直接舒张血管作用所致。在本研究中,不同浓度(10(-8)-10(-4)M)的丙泊酚均未在主动脉环中诱导任何收缩反应。较低浓度(10(-8)-10(-6)M)的丙泊酚对苯肾上腺素诱导的收缩无显著影响,但在较高浓度(10(-5)-10(-4)M)时,丙泊酚对完整内皮和去内皮环的抑制作用均显著。用丙泊酚(10(-6)和10(-5)M)预处理完整内皮环可降低乙酰胆碱的舒张作用。本研究结果表明,临床相关浓度的丙泊酚(10(-6)M或更低)无直接舒张血管作用,且会降低对乙酰胆碱的内皮依赖性舒张作用。

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