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作 者:王淑英[1] 王建刚[1] 李艳[1] 路西明[1] 吴银萍
机构地区:[1]洛阳医学高等专科学校药理教研室
出 处:《河南医学研究》1999年第1期11-12,共2页Henan Medical Research
基 金:河南省科委资助
摘 要:目的:探讨脑脉舒宁降压作用的机理。方法:采用大鼠胸主动脉条测定脑脉舒宁对去甲肾上腺素(NE)、CaCl2的量效曲线以及对单剂量氯化钾所致收缩的影响。结果:脑脉舒宁能使NE、CaCl2的量效曲线右移,最大反应压低,呈非竞争性拮抗;同时也可抑制高钾去极化引起的血管条收缩。结论:脑脉舒宁松弛血管平滑肌的作用与拮抗Ca2+有关。Objective: To explore the mechanism blood lowering effect of Naomaishuning.Methods: The effect of Naomaishuning on the contraction isolated rat aortic strips induced by calcium,norepinephrine and potassium.Results: The results showed that Naomaishuning shifted the cumulative concentration response curves for CaCl 2 and norepinephrine to right,and depressed their maximal responses.It appeared that the Naomaishuning was noncompetitive antagonist to CaCl 2 and norepinephrine,Naomaishuning also inhibited the contration of aortic strips evoked by single dose of KCl.Conclusion:The results suggested that Naomaishuning block calcium channels.
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