Long-term administration of Salvia miltiorrhiza ameliorates carbon tetrachloride-induced hepatic fibrosis in rats

被引:38
作者
Lee, TY
Wang, GJ
Chiu, JH
Lin, HC
机构
[1] Vet Gen Hosp, Dept Med, Div Gastroenterol, Taipei 11217, Taiwan
[2] Natl Yang Ming Univ, Sch Med, Inst Tradit Med, Taipei 112, Taiwan
[3] Natl Res Inst Chinese Med, Taipei, Taiwan
关键词
D O I
10.1211/0022357022098
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Carbon tetrachloride (CCl4) is metabolized by cytochrome P450 to form a reactive trichloromethyl radical that triggers a chain of lipid peroxidation. These changes lead to cell injury, and chronic liver injury leads to excessive deposition of collagen in liver, resulting in liver fibrosis. The aim of this study was to evaluate the effects of long-term Salvia miltiorrhiza administration in CCl4-induced hepatic injury in rats. Salvia miltiorrhiza (10, 25 or 50 mg kg(-1) twice a day) was given for 9 weeks, beginning at the same time as the injections Of CCl4. Rats receiving CCl4 alone showed a decreased hepatic glutathione level and an increased glutathione-S-transferase content. The hepatic thiobarbituratic acid-reactive substance levels were increased. CCl4 also caused a prominent collagen deposition in liver histology that was further supported by the increased hepatic mRNA expression of transforming growth factor-beta1, tissue inhibitor of metallproteinase-1 and procollagen 1. Salvia miltiorrhiza administration led to a dose-dependent increase in hepatic glutathione levels and a decrease in peroxidation products. Additionally, it reduced the mRNA expression of markers for hepatic fibrogenesis. In conclusion, long-term administration of Salvia miltiorrhiza in rats ameliorated the CCl4-induced hepatic injury that probably related to a reduced oxidant stress and degree of hepatic fibrosis.
引用
收藏
页码:1561 / 1568
页数:8
相关论文
共 34 条
[1]   A SYSTEMATIC-APPROACH FOR DESIGN AND PLANNING OF MECHANICAL ASSEMBLIES [J].
CHEN, CLP ;
WICHMAN, CA .
AI EDAM-ARTIFICIAL INTELLIGENCE FOR ENGINEERING DESIGN ANALYSIS AND MANUFACTURING, 1993, 7 (01) :19-36
[2]  
CONNOR HD, 1990, MOL PHARMACOL, V37, P443
[3]   Glutathione levels discriminate between oxidative stress and transforming growth factor-β signaling in activated rat hepatic stellate cells [J].
De Bleser, PJ ;
Xu, GX ;
Rombouts, K ;
Rogiers, V ;
Geerts, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (48) :33881-33887
[4]   VITAMIN-A POTENTIATION OF CARBON-TETRACHLORIDE HEPATOTOXICITY - ROLE OF LIVER MACROPHAGES AND ACTIVE OXYGEN SPECIES [J].
ELSISI, AED ;
EARNEST, DL ;
SIPES, IG .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1993, 119 (02) :295-301
[5]   LIPID-PEROXIDATION MEASURED AS THIOBARBITURIC ACID-REACTIVE SUBSTANCES IN TISSUE-SLICES - CHARACTERIZATION AND COMPARISON WITH HOMOGENATES AND MICROSOMES [J].
FRAGA, CG ;
LEIBOVITZ, BE ;
TAPPEL, AL .
FREE RADICAL BIOLOGY AND MEDICINE, 1988, 4 (03) :155-161
[6]   Molecular regulation of hepatic fibrosis, an integrated cellular response to tissue injury [J].
Friedman, SL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (04) :2247-2250
[7]   Effects of S-adenosylmethionine on lipid peroxidation and liver fibrogenesis in carbon tetrachloride-induced cirrhosis [J].
Gasso, M ;
Rubio, M ;
Varela, G ;
Cabre, M ;
Caballeria, J ;
Alonso, E ;
Deulofem, R ;
Camps, J ;
Gimenez, A ;
Pajares, M ;
Pares, A ;
Mato, JM ;
Rodes, J .
JOURNAL OF HEPATOLOGY, 1996, 25 (02) :200-205
[8]  
Herbst H, 1997, AM J PATHOL, V150, P1647
[9]   The protective effects of PMC against chronic carbon tetrachloride-induced hepatotoxicity in vivo [J].
Hsiao, G ;
Lin, YH ;
Lin, CH ;
Chou, DS ;
Lin, WC ;
Sheu, JR .
BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2001, 24 (11) :1271-1276
[10]  
Huang YL, 2000, J DENT RES, V79, P214