Planta Med 2006; 72(13): 1250-1253
DOI: 10.1055/s-2006-947223
Letter
© Georg Thieme Verlag KG Stuttgart · New York

A Ginsenoside Metabolite, 20-O-β-D-Glucopyranosyl-20(S)-protopanaxadiol, Triggers Apoptosis in Activated Rat Hepatic Stellate Cells via Caspase-3 Activation

Eun-Jeon Park1 , Yu-Zhe Zhao1 , Jaebaek Kim2 , Dong Hwan Sohn1
  • 1Department of Pharmacy, Wonkwang University, Iksan, Jeonbuk, Republic of Korea
  • 2Wonkwang Pharmaceutical Co., Ltd., Iksan, Jeonbuk, Republic of Korea
Further Information

Publication History

Received: June 1, 2006

Accepted: July 2, 2006

Publication Date:
18 September 2006 (online)

Abstract

We investigated the apoptotic effects of the protopanaxadiol ginsenosides, Rb1 and Rb2, and their intestinal bacterial metabolite, 20-O-β-D-glucopyranosyl-20(S)-protopanaxadiol (M1), and of the protopanaxatriol ginsenoside, Rg1, and its intestinal bacterial metabolite, 20(S)-protopanaxatriol, in activated rat hepatic stellate cells (HSCs) transformed by Simian virus 40 (T-HSC/Cl-6). As HSCs play a central role in liver fibrosis, agents that selectively induce apoptosis of HSCs could be used to treat this disease. Apoptosis was measured using cell viability tests, DNA fragmentation analysis, and immunoblot analysis of poly(ADP-ribose) polymerase cleavage. M1 (40 μM for 24 h) significantly induced apoptosis in activated rat HSCs. M1 induced apoptosis in a dose-dependent manner as shown by DNA fragmentation, an increased population of cells in the sub-G1 phase, and reduced mitochondrial transmembrane potential. M1 induced caspase-3 activity in a dose- and time-dependent manner. A specific inhibitor of caspase-3 prevented induction of apoptosis by M1 as shown by DNA fragmentation analysis. It is concluded that M1 induces apoptosis in T-HSC/Cl-6 cells via caspase-3 activation.

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Prof. Dong Hwan Sohn

Department of Pharmacy

Wonkwang University

Iksan

Jeonbuk 570-749

Republic of Korea

Fax: +82-63-854-6038

Email: dhsohn@wonkwang.ac.kr

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