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三七中分离得到的人参二醇皂苷对细胞内、外钙的影响

[Effects of panaxadiol saponins isolated from Panax notoginseng on intracellular and extracellular calcium].

作者信息

Dan H X, Zhang B H, Xie S R, Yao J A, Jia J N

机构信息

Department of Pharmacology, School of Basic Medical Sciences, Beijing Medical University, China.

出版信息

Zhongguo Yao Li Xue Bao. 1993 Nov;14 Suppl:S22-5.

PMID:8010067
Abstract

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+.

摘要

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。

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