Basic Research
Copyright ©The Author(s) 2004. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Oct 1, 2004; 10(19): 2831-2835
Published online Oct 1, 2004. doi: 10.3748/wjg.v10.i19.2831
Effects of herbal compound 861 on human hepatic stellate cell proliferation and activation
Lin Wang, Jian Wang, Bao-En Wang, Pei-Gen Xiao, Yan-Jiang Qiao, Xue-Hai Tan
Lin Wang, Yan-Jiang Qiao, School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing 100102, China
Xue-Hai Tan, Jian Wang, Beijing Genomic Institute, Beijing 101300, China
Bao-En Wang, Liver Research Center, Beijing Friendship Hospital, Capital University of Medical Sciences, Beijing 100050, China
Pei-Gen Xiao, Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences, Beijing 100094, China
Author contributions: All authors contributed equally to the work.
Supported by the Fund of One Hundred Scientist Plan of Chinese Academy of Sciences and the Knowledge Innovation Program Foundation of Chinese Academy of Sciences, No. KSCX2-SW-207
Correspondence to: Dr. Xue-Hai Tan, Beijing Genomic Institute, Beijing 101300, China. tanxh@genomics.org.cn
Telephone: +86-10-80481755 Fax: +86-10-80498676
Received: March 23, 2004
Revised: April 9, 2004
Accepted: April 16, 2004
Published online: October 1, 2004
Abstract

AIM: To investigate the effects of herbal compound 861 (Cpd 861) on cell proliferation in human hepatic stellate cells (LX-2) and human hepatocellular liver carcinoma cells (HepG2), and expression of α-smooth muscle actin (α-SMA) in LX-2 cells.

METHODS: LX-2 and HepG2 cells were incubated with various concentrations of Cpd 861 (0.1-0.003 mg/mL) for 1, 2, 3, 5 and 7 d. Cell proliferation was analyzed by 3-(4, 5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium (MTS) assay. Effects of Cpd861 on the expression of α-SMA mRNA in LX-2 cells were measured by real-time quantitative PCR method using SYBR Green I technology.

RESULTS: Cpd 861, at 0.1 mg/mL, significantly inhibited LX-2 cell proliferation (15% decrease relative to control, P < 0.05) after 3 d of incubation. The inhibitory effects seemed to increase with the treatment time (25% decrease after 5 d of incubation and 35% decrease after 7 d of incubation, P < 0.01). However, Cpd 861 did not affect HepG2 cell proliferation at the same concentration used for LX-2 cells. The expression levels of α-SMA mRNA decreased significantly when LX-2 cells were exposed to Cpd 861 for 48 h (59% decrease relative to control, P < 0.05) or 72 h (60% decrease relative to control, P < 0.01).

CONCLUSION: Cpd 861 can significantly inhibit LX-2 cell proliferation in a dose-dependant manner, and reduce the expression levels of α-SMA mRNA in LX-2 cells. Since hepatic cell proliferation and high level of α-SMA are associated with liver fibrosis, the results suggest that Cpd 861 may be useful in the treatment of this disease.

Keywords: $[Keywords]