Fujiwara T, Chiba S
1st Department of Internal Medicine, Shinshu University School of Medicine, Nagano, Japan.
Eur J Pharmacol. 1994 Jun 13;258(3):195-205. doi: 10.1016/0014-2999(94)90481-2.
The vascular responsiveness to histamine, 2-pyridylethylamine and dimaprit was investigated in isolated and perfused atherosclerotic rabbit common carotid arteries enclosed by a hollow silastic collar. The constrictor effects of histamine were significantly enhanced in atherosclerotic arteries, although those of 2-pyridylethylamine were not changed. The dilator effects of histamine and dimaprit, which were completely inhibited after pretreatment with cimetidine, were not influenced by removal of the endothelium but significantly depressed in atherosclerotic arteries. The dose-response curves for histamine in the control group pretreated with cimetidine were shifted to the left and responses reached almost the same level as those of the atherosclerotic group. From these results, it is concluded that histamine-induced vasoconstrictions are enhanced in atherosclerotic arteries, and that the mechanism of the hyperreactivity to histamine might be an attenuation of the vasodilatations mediated via histamine H2 receptors in vascular smooth muscle.
在被中空硅橡胶套包围的离体灌流动脉粥样硬化兔颈总动脉中,研究了对组胺、2-吡啶乙胺和地马普明的血管反应性。尽管2-吡啶乙胺对动脉粥样硬化动脉的收缩作用未改变,但组胺的收缩作用在动脉粥样硬化动脉中显著增强。组胺和地马普明的舒张作用在用西咪替丁预处理后被完全抑制,不受内皮去除的影响,但在动脉粥样硬化动脉中显著降低。用西咪替丁预处理的对照组中组胺的剂量-反应曲线向左移动,反应达到与动脉粥样硬化组几乎相同的水平。从这些结果得出结论,组胺诱导的血管收缩在动脉粥样硬化动脉中增强,并且对组胺高反应性的机制可能是血管平滑肌中通过组胺H2受体介导的血管舒张减弱。