Li Q P, Liu T P
Department of Pharmacology, Nanjing Medical College, China.
Zhongguo Yao Li Xue Bao. 1992 Sep;13(5):407-11.
The effect of tetrandrine (Tet), a calcium antagonist, on the maximal upstroke velocity (Vmax) of depolarization in K(+)-depolarized guinea pig papillary muscles was studied by standard microelectrode method with computer. The results showed that: (1) the resting block of Tet on Vmax was concentration dependent; (2) the drug (50 or 100 mumol.L-1) caused a marked frequency-dependent block of Vmax, which accounted for 65 +/- 8% of total block at a concentration of 100 mumol.L-1 and the pacing frequency of 0.3 Hz; (3) the recovery kinetics of Vmax could be characterized as a biexponential function, of which the second phase was prolonged by the drug; (4) compared with verapamil, nitrendipine, and diltiazem, the above-mentioned effects of Tet on Vmax were similar to those of diltiazem. These results suggest that Tet can block calcium channel in both frequency-dependent and frequency-independent manner, mainly the former.
采用标准微电极方法结合计算机,研究了钙拮抗剂粉防己碱(Tet)对钾离子去极化豚鼠乳头肌动作电位最大除极速度(Vmax)的影响。结果表明:(1)Tet对Vmax的静息阻滞呈浓度依赖性;(2)该药物(50或100μmol·L-1)引起Vmax明显的频率依赖性阻滞,在浓度为100μmol·L-1、起搏频率为0.3Hz时,频率依赖性阻滞占总阻滞的65±8%;(3)Vmax的恢复动力学可表征为双指数函数,药物可延长其第二相;(4)与维拉帕米、尼群地平和地尔硫䓬相比,Tet对Vmax的上述作用与地尔硫䓬相似。这些结果提示,Tet可通过频率依赖性和非频率依赖性方式阻断钙通道,主要以前者为主。