摘要
目的:观察独活肠吸收液对大鼠离体胸主动脉环的舒张作用及其舒张机制。方法:应用外翻肠囊法制备独活含药肠吸收液,采用离体血管环技术制备大鼠胸主动脉环,使用累积加药法分别检测独活肠吸收液对PE、KCl刺激的内皮完整与去内皮胸主动脉环张力的影响,并探讨其Ca2+调节机制。结果:独活肠吸收液能够浓度依赖性地舒张PE、KCl引起的内皮完整与去内皮血管环收缩,内皮完整组与去内皮组最大舒张率比较差异无统计学意义。对PE或KCL预收缩的血管,独活肠吸收液均能抑制Ca Cl2所致最大收缩效应。结论:独活肠吸收液对PE、KCl引起的血管收缩均具有较好的舒张作用并呈剂量依赖性,其作用机制与抑制细胞外Ca2+内流密切相关。
Objective: To observe the vasodilatation effect of intestinal absorption solution of Angelica Pubescens on thoracic aorta and its related mechanism. Methods: Intestinal absorption solution of Angelica Pubescens was prepared by everted gut sac method in vitro. To investigate the influence and the calcium-related mechanisms of intestinal absorption solution of Angelica Pubescens on endothelium intact or endothelium denuded with PE and KCl. Results: Intestinal absorption solution of Angelica Pubescens could produce relaxation of thoracic aortic rings pre-contracted by PE and KCl with endothelium intact or denuded in a dose dependent manner. There was no significant difference between the endothelium intact group and the endothelium denuded group. Intestinal absorption solution of Angelica Pubescens inhibit Ca Cl2-induced maximum contraction effect. Conclusion: Intestinal absorption solution of Angelica Pubescens shows vasodilator effects on a dose-dependent manner. The vasodilatation effect is mediated by inhibition of extracellular Ca2 +influx.
引文
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