Your browser doesn't support javascript.
loading
Hepatoprotective mechanisms of Yan-gan-wan.
Yang, Melissa D; Deng, Qing-Gao; Chen, Shuang; Xiong, Shigang; Koop, Dennis; Tsukamoto, Hidekazu.
Afiliação
  • Yang MD; Research Center for Alcoholic Liver and Pancreatic Diseases and Department of Pathology, Keck School of Medicine of the University of Southern California, VA Greater Los Angeles Healthcare System, 1333 San Pablo Street, MMR-412, Los Angeles, CA 90089-9141, USA.
Hepatol Res ; 32(4): 202-12, 2005 Aug.
Article em En | MEDLINE | ID: mdl-16107322
ABSTRACT
BACKGROUND AND

AIMS:

A herbal prescription, Yan-gan-wan (YGW), has been known to offer hepatoprotective effects in Asian countries for years. This study investigated its mechanisms of action.

METHODS:

The effects of YGW on CCl(4) induced liver damage were tested in mice and cultured hepatocytes. Microarray analysis screened genes affected by YGW. YGWs effects on the expression of cytochrome P450 (CYP) 2E1 and other isozymes were determined. YGWs effects on TNFalpha expression and NF-kappaB activation in Kupffer cells (KC), and TNFalpha promoter activity in RAW264.7 cells, were also assessed.

RESULTS:

Administration of YGW reduced the plasma ALT, centrilobular necrosis, neutrophilic infiltration, and TNFalpha mRNA in the livers of mice acutely given CCl(4). The in vivo herb treatment reduced ALT release and necrosis of isolated hepatocytes directly exposed to CCl(4). Microarray analysis demonstrated marked reductions in CYP4A10 and 4A14 by YGW but no changes in other CYP isozymes as confirmed by immunoblot analysis. The herb treatment suppressed LPS-stimulated TNFalpha release in vivo and by cultured KC. Direct addition of the aqueous herb extract suppressed NF-kappaB activation by KC and TNFalpha promoter activity in RAW cells under LPS stimulation. This activity to suppress TNFalpha expression was largely separated into gel filtration fractions with the molecular size of 102-107Da. YGW also attenuated liver fibrosis induced by chronic treatment of CCl(4) or porcine serum.

CONCLUSIONS:

The protective effects of YGW on CCl(4) hepatotoxicity are due in part to inhibition of KC NF-kappaB activation and TNFalpha expression by small water soluble molecules, and may also be related to suppressed hepatic expression of CYP4A10 and 4A14 that are considered as alternative prooxidant cytochromes.
Buscar no Google
Base de dados: MEDLINE Idioma: En Revista: Hepatol Res Ano de publicação: 2005 Tipo de documento: Article País de afiliação: Estados Unidos
Buscar no Google
Base de dados: MEDLINE Idioma: En Revista: Hepatol Res Ano de publicação: 2005 Tipo de documento: Article País de afiliação: Estados Unidos