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作 者:徐尚忠[1,2,3] 张翼[1,2,3] 任建英[1,2,3] 周兆年
机构地区:[1]上海市徐汇区中心医院心血管病研究室 [2]河北医科大学生理学教研室 [3]中国科学院上海生理研究所
出 处:《中国药理学报》1997年第6期518-518,共1页Acta Pharmacologica Sinica
摘 要:目的:研究小檗碱(Ber)对心室肌细胞钙通道的影响.方法:全细胞膜片箝技术.结果:Ber(10,30μmol·L-1)使豚鼠心室肌细胞L型钙流由1400±247pA分别减至978±204pA及617±23pA(n=5,P<005),抑制效应呈浓度依赖及非频率依赖,其电流-电压曲线的峰值下降.Ber(10μmol·L-1)使L型钙流失活曲线的最大半激活电压由-278mV变为-342mV,斜率因子由922变为1303,对激活曲线无影响.Ber(10,30μmol·L-1)使T型钙流峰值由加药前的154±80pA降至101±78pA及48±45pA(n=8,P<005).结论:Ber对L和T型钙通道均有抑制作用.IM: To study the effects of berberine (Ber) on L ( I Ca,L ) and T type ( I Ca,T ) channels in isolated guinea pig ventricular myocytes. METHODS: Using whole cell patch clamp recording technique. RESULTS: Ber 10, 30 μmol·L -1 inhibited the I Ca, L from 1400±247 pA to 978±204 pA ( n =5 cells of 5 guinea pigs, P <0 05), and to 664±179 pA ( n =5, P <0 01), respectively. The inhibitory effect was concentration dependent and non frequency dependent. The peak value of I Ca,L in the current voltage relationship was decreased. Ber affected the inactivation kinetics of I Ca,L . The half activation potential ( V 0 5 ) was shifted from -27 8 mV to -34 2 mV and the slope factor (κ) was changed from 9 22 into 13 03. Ber did not affect the activation kinetics. Ber 10 and 30 μmol·L -1 also inhibited I Ca,T (from 154±80 pA to 101±78 pA, and to 48±45 pA, n =8 cells of 5 guinea pigs, P <0 05).CONCLUSION: Ber possessed blocking effects on both L and T type calcium channels.
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