TETRANDRINE - A NOVEL CALCIUM-CHANNEL ANTAGONIST INHIBITS TYPE-I CALCIUM CHANNELS IN NEUROBLASTOMA-CELLS

被引:42
作者
LIU, QY
KARPINSKI, E
RAO, MR
PANG, PKT [1 ]
机构
[1] UNIV ALBERTA,FAC MED,DEPT PHYSIOL,EDMONTON T6G 2H7,ALBERTA,CANADA
[2] NANJING MED COLL,DEPT CARDIOVASC PHARMACOL,NANJING,PEOPLES R CHINA
关键词
TETRANDRINE; TYPE-I CALCIUM CURRENT; NEUROBLASTOMA CELL;
D O I
10.1016/0028-3908(91)90030-F
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Tetrandrine, an alkaloid isolated from the Chinese herb, Radix stephaniae tetrandrae, has been used clinically as a hypotensive agent for a long time. Recently, several studies have demonstrated that tetrandrine behaves like a calcium entry blocker. In the present investigation, the whole cell version of the patch clamp technique was used to study the effect of tetrandrine on the type I (transient inward) calcium current in neuroblastoma cells. These results showed that tetrandrine inhibited the transient inward current, without affecting the channel kinetics. The effects of tetrandrine were dose-dependent and reversible but did not depend on the frequency of stimulation (use-dependence) or the membrane potential. These data clearly demonstrate that tetrandrine is a novel and potent antagonist of the transient inward current in neuroblastoma cells.
引用
收藏
页码:1325 / 1331
页数:7
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