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作 者:肖洪涛[1,2] 廖治[3] 韩彬[2] 陈淑杰[2] 莫正纪[2]
机构地区:[1]四川省医学科学院.四川省人民医院药剂科,成都610072 [2]四川大学华西药学院,成都610041 [3]四川省医学科学院.四川省人民医院妇产科,成都610072
出 处:《中国新药杂志》2009年第2期163-166,共4页Chinese Journal of New Drugs
摘 要:目的:评价盐酸戊乙奎醚对离体大鼠子宫收缩的影响。方法:采用乙酰胆碱(Ach)致大鼠离体子宫痉挛模型,测量给予盐酸戊乙奎醚后大鼠离体子宫条痉挛收缩的最大张力,用经典的Schild方法计算受试药的pA2值。实验同时使用非选择性胆碱受体阻滞剂阿托品和选择性M2受体阻滞剂加那胺(gallam ine)作阳性对照药。结果:盐酸戊乙奎醚的pA2值显著大于硫酸阿托品pA2值[(12.19±1.10)vs(9.36±2.30),P<0.05],与加那胺的pA2值接近(12.49±2.20)。盐酸戊乙奎醚对离体大鼠子宫抗Ach痉挛的松弛作用强度明显大于硫酸阿托品。结论:盐酸戊乙奎醚能有效地缓解离体大鼠子宫的痉挛状态。Objective: To investigate the effect of penehyclidine hydrochloride (PHC) on contraction in rat uterus. Methods: The contraction of isolated rat uterus was induced by acetylcholine. The maximum amplitude of contractions was measured after exposure to PHC, atropine (a non-selective M receptor antagonist) and gallamine (an M2 receptor antagonist). The pA2 value was determined by Schild assay. Results: According to pA2 values, the antagonizing effect of PHC on acetylcholine-induced contraction in isolated rat uterus was stronger than that of atropine [ (12.19±1.10) vs (9.36±2.30), P 〈0.05 ], and was similar to that of gallamine (12.49 ±2.20). Conclusion: PHC can effectively relieve uterus contraction in vitro.
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