Dan H X, Zhang B H, Xie S R, Yao J A, Jia J N
Department of Pharmacology, School of Basic Medical Sciences, Beijing Medical University, China.
Zhongguo Yao Li Xue Bao. 1993 Nov;14 Suppl:S22-5.
Panaxadiol saponins (PDS) contain saponins Panax notoginseng B1 and E. The spontaneous beating induced by isoproterenol in isolated rat right atria and the increase of contractile force induced by Ca2+ in isolated guinea pig colon were inhibited by PDS 75 and 150 micrograms.ml-1, respectively and perhexiline 6.25 and 12.5 mumol.L-1, respectively. It suggested that PDS could block the potential-dependent and receptor-operated calcium channel in smooth muscle. PDS 150 micrograms.ml-1 and perhexiline 6.25 mumol.L-1 depressed the contractile force induced by norepinephrine and Ca2+ in isolated rat aortic strips in Ca(2+)-free Krebs' solution. It suggested that PDS and perhexiline not only inhibited the release of intracellular Ca2+ but also blocked the inflow of extracellular Ca2+.
人参二醇皂苷(PDS)含有三七皂苷B1和E。在离体大鼠右心房中,75和150微克/毫升的PDS分别抑制了异丙肾上腺素诱导的自发搏动,在离体豚鼠结肠中,PDS分别抑制了由Ca2+诱导的收缩力增加,6.25和12.5微摩尔/升的哌克昔林也分别有此作用。这表明PDS可阻断平滑肌中的电压依赖性和受体操纵性钙通道。在无Ca2+的Krebs溶液中,150微克/毫升的PDS和6.25微摩尔/升的哌克昔林抑制了去甲肾上腺素和Ca2+在离体大鼠主动脉条中诱导的收缩力。这表明PDS和哌克昔林不仅抑制细胞内Ca2+的释放,还阻断细胞外Ca2+的流入。