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作 者:孙成文[1] 赵春燕[1] 钟国赣[1] 王晓明[1] 江岩[1] 杨世杰[1]
机构地区:[1]白求恩医科大学生理教研室,白求恩医科大学生理中心实验室,白求恩医科大学药理教研室
出 处:《基础医学与临床》1994年第4期46-50,共5页Basic and Clinical Medicine
摘 要:应用细胞封接式膜片钳方法,在Wistar大鼠的单个心室肌细胞上,观察了人参二醇组皂甙Rc(ginsenoside-Rc),Rd(ginsenoside-Rd)200μg/ml对钙通道单通道活动的影响,并与钙通道阻滞剂异搏定37.5μg/ml、钙通道激动剂BAYK8644μmmol/L对照,证明Rc对钙通道有阻滞作用;而Rd则无此作用。用电子自旋共振法(electronspinresonance,ESR)测定了培养心肌细胞的自由基含量,Rc30μg/ml能显著抑制黄嘌呤0.42mmol/L-黄嘌呤氧化酶5.3nmol/L所致的自由基含量的增多:而Rd30μg/ml对其影响则不明显。he effects of Rc, Rd 200μg/ml to single Ca2+channel on ventricular myocar-diocytes of Wistar rats Were recorded using the cell-attached configuration of thepatch clamp technique,and compared with calcium channel blocker verapamil 37.5μg/ml and calcium channel activator BAY K 8644 5μmmol/ml. Panaxadiol saponinmonomer Rc 200μg/ml inhibited the activities of T,L and B type of calciumchannel significantly,whill Rd 200μg/ml have no this effect. Electron spin reso-nance was used to measure the free radical contents of the cultured cardiomyocytes.Rc 30 μg/ml signif icantly reduce the increased free radical content indued by xanth-ine 0.42mmol/L-xanthine oxidase 5. 3nmol/L, but Rd 30μbg/ml no this effect.
分 类 号:R282.710.5[医药卫生—中药学]
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