Objective To investigate the effects of propofol on the isolated rat aorta to explore the relationship between propofol and ATP-sensitive K + channel(K ATP ) and the mechanisms. Methods The effects of propofol and DMSO on norepinephrine (NE)-induced vasoconstriction were determined in the isolated rat aortic rings under varied circumstances:in calciferous or noncalciferous K-H solutions,with or without intact endothelium,in the presence or absence of glibenclamide(the specific antagonist of K ATP ). Results DMSO showed no obvious effects in all of the experimental conditions. Propofol at 100 μg·ml -1 dilated the NE-pretreated aorta by 58%(P0.01). This effect was also observed in noncalciferous solution and in ex-endothelium condition,and could be partially antagonised by glibenclamide(P0.01).Conclusions The vasodilatory effect of propofol on isolated rat aortic rings is related to the modulation of K ATP ,through which the extracellular Ca 2+ influx and/or the release of intracellular Ca 2+ are depressed. The drug acts directly on the vascular smooth muscle,which may be independent of intact endothelium and extracellular Ca 2+ .