Liu Q Y, Karpinski E, Pang P K
Department of Physiology, University of Alberta, Edmonton, Canada.
J Cardiovasc Pharmacol. 1992 Oct;20(4):513-9. doi: 10.1097/00005344-199210000-00001.
Tetrandrine, a putative Ca2+ channel blocker, is extracted from the Chinese medicinal herb, Radix stephania tetrandrae. In the present study, the whole-cell version of the patch clamp technique was used to investigate the effects of tetrandrine on both T and L calcium channel currents in primary cultured neonatal rat ventricular cells. We show that tetrandrine inhibits both T and L calcium channel currents in ventricular cells. This inhibition of inward Ca2+ currents is concentration dependent and reversible. Tetrandrine does not shift the I-V relationship of the calcium currents. These results clearly demonstrate that tetrandrine acts as a calcium channel antagonist in ventricular cells. Previous data show that tetrandrine may be regarded as a wide-spectrum calcium channel antagonist.
粉防己碱是一种公认的钙离子通道阻滞剂,从中药粉防己中提取。在本研究中,采用膜片钳技术的全细胞模式,研究粉防己碱对原代培养新生大鼠心室肌细胞T型和L型钙通道电流的影响。我们发现粉防己碱可抑制心室肌细胞的T型和L型钙通道电流。这种对内向钙离子电流的抑制呈浓度依赖性且可逆。粉防己碱不改变钙电流的I-V关系。这些结果清楚地表明,粉防己碱在心室肌细胞中作为钙通道拮抗剂发挥作用。先前的数据表明,粉防己碱可被视为一种广谱钙通道拮抗剂。