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作 者:庞敏霞[1] 余芳[1] 陈素红[2] 苏洁[1] 陈琦[1] 吕圭源[1]
机构地区:[1]浙江中医药大学,杭州310053 [2]温州医学院,温州325035
出 处:《中药药理与临床》2013年第5期118-121,共4页Pharmacology and Clinics of Chinese Materia Medica
基 金:国家自然科学基金(81274123);国家"重大新药创制"科技重大专项(2011ZX09101-002-07;2009ZX09502-016);浙江省卫生高层次创新人才培养工程项目(浙卫发[2010]190号)
摘 要:目的:观察复方菊明对大鼠离体胸主动脉环收缩作用的影响。方法:采用离体血管张力实验法,观察复方菊明、维拉帕米(Ver)和生理盐水对NA、高K+液引起的主动脉环收缩的影响,以及对NA诱导的主动脉环依赖细胞内钙与外钙收缩的影响。结果:复方菊明(4.0mg/ml^8.0mg/ml)和Ver能拮抗NA(2.37μmol/l)和KCl(2.37μmol/l)诱导的主动脉环收缩作用,生理盐水无影响。在相同的浓度下,复方菊明拮抗NA诱导的主动脉环收缩作用比对KCl诱导的主动脉环收缩的拮抗作用强。此外,复方菊明(5.0mg/ml)对NA诱导的依赖细胞内钙、外钙的收缩均有抑制,Ver对NA诱导的依赖细胞内钙的收缩有抑制作用、对依赖细胞外钙的收缩没有影响;生理盐水组给药前后没有变化。结论:复方菊明具有直接舒张血管作用,能阻断受体依赖性钙通道(ROC)和电压依赖性钙通道(VDC),其降压机制可能通过阻断ROC,抑制内钙释放外钙内流,从而降低胞内Ca2+浓度,发挥降压作用。To investigate the effect of Compound flos Chrysanthemi indici and Semen eassiae (FJM) in contracting isolated thoracic a orta tings in the rats. Method: Isolated vascular tension experiment were operated to respectively observe the effect of FJM, Ver, NS on aorta rings contraction induced by NA and high level of K +. Also, study its effect on intracellular and extracellular Ca^2+ -dependent aorta rings contraction, induced by NA. Result: FJM(4.0mg/ml ~ 8.0mg/ml)and Ver could inhibit the contraction of aortic ring evoked by NA(2. 37 μmol/l)or KCI (40mmol/1) (P 〈 0.01 ), NS has no inhibition. In the same concentrations, the inhibition effect of aortic ring evoked by NA is more obvious than that evoked by KC1. FJM (5.0mg/ml)could also inhibit intraeellular and extracellular Ca^2+ -dependent contraction, induced by NA(P 〈0.01 ). Ver(5 x 10-3 mg/ml)could inhibit intracellular Ca^2+-dependem contraction, induced by NA. NS shows no change. Conclusion: FJM could directly constrict blood vessels. Inhibition of receptor operated calcium channel(ROC) and voltage-depend ent calcium channel(VDC)were also observed. The mechanism of antihypertensive possibly due to block ROC and inhibit internal Ca^2+ re- lease and external Ca^2 + influx, therefore reduce Ca^2+ concentration in the cell.
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