莪术醇对大鼠十二指肠平滑肌收缩的影响  

Effects of curcumol on contraction of duodenal smooth muscle in rats

作　　者：金龙[1] 马建秀[1] 马艳庆[1] JIN Long;MA Jian xiu;MA Yan qing(Medical College of Northwest Minzu University, Lanzhou730030, China)

机构地区：[1]西北民族大学医学院,兰州甘肃730030

出　　处：《中国药理学通报》2017年第12期1717-1720,共4页Chinese Pharmacological Bulletin

基　　金：2016年度中央高校基本科研业务经费专项资金项目(No31920160066)

摘　　要：目的观察莪术醇(curcumol)对大鼠离体十二指肠平滑肌收缩活动的影响,并探讨其可能的作用机制。方法制作大鼠离体十二指肠标本,用恒温灌流的方法,使用BL-420F生物机能实验系统观察不同浓度莪术醇对大鼠离体十二指肠平滑肌收缩的影响。选取一定浓度莪术醇分别与阿托品、异丙肾上腺素、去甲肾上腺素、无钙Krebs液、维拉帕米共同孵育,观察其对平滑肌收缩的作用。结果莪术醇可兴奋离体十二指肠平滑肌,使其收缩振幅和张力明显增大,该作用可被阿托品、异丙肾上腺素、去甲肾上腺素、维拉帕米部分拮抗。结论莪术醇具有明显促进大鼠离体十二指肠平滑肌收缩的作用,其可能是通过兴奋M受体、抑制α和β受体、促进外钙内流实现。AimTo investigate the effects of curcumol on the contractile activity of isolated duodenal smooth muscle in rats and explore its underlying mechanisms.MethodsThe isolated duodenum specimens of rats were made.The effects of different concentrations of curcumol on the contraction of isolated duodenal smooth muscle were observed using BL420F biological and functional experimental system with constant temperature perfusion method.A certain concentration of curcumol was combined with atropine,isoproterenol,norepinephrine,calcium free Krebs solution,verapamil respectively to observe its effect on smooth muscle contraction.ResultsCurcumol could stimulate duodenal smooth muscle in vitro,and increase its contractile amplitude and tension significantly.It could be antagonized partly by atropine,isoprenaline,norepinephrine,verapamil.ConclusionCurcumol can promote the contraction of isolated duodenal smooth muscle in rats,which may be achieved by stimulating M receptor,inhibitingαandβreceptors,and promoting the extracellular calcium influx.

关 键 词：莪术醇 十二指肠平滑肌 M受体 Β受体 Α受体 CA2+ 大鼠 

分 类 号：R-332[医药卫生] R284.1