Protective mechanism of Salvia miltiorrhiza on carbon tetrachloride-induced acute hepatotoxicity in rats

被引:0
作者
Lee, TY
Mai, LM
Wang, GJ
Chiu, JH
Lin, YL
Lin, HC
机构
[1] Taipei 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 Yang Ming Univ, Inst Anat, Taipei 112, Taiwan
[4] Natl Res Inst Chinese Med, Taipei, Taiwan
关键词
Salvia miltiorrhiza; carbon tetrachloride; cytochrome P450; glutathione; nitric oxide;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The purpose of this study was to investigate the possible mechanisms of Salvia miltiorrhiza (Sm) in carbon tetrachloride (CCl4)-induced acute hepatotoxicity in rats. Male Wistar rats received a single dose Of CCl4 (2 ml/kg in corn oil, intraperitoneally). Three hours after CCl4 intoxication, rats received either Sm (100mg/kg) or silymarin (100mg/kg) by gastrogavage twice a day for 2 consecutive days. CCl4-induced liver damage was shown by significant elevation of serum aminotransferase levels. Additionally, a significant decrease was observed in hepatic microsomal P450 2E1 protein content and hepatic concentrations of antioxidant enzymes. In contrast, rats given both Sm and silymarin supplement had less elevation of serum aminotransferase concentrations associated with less severe lobular damage of hepatocytes than rats receiving CCl4 alone. Sm administration restored the reduction of hepatic microsomal P450 2E1 protein content as well as inducing an increase in hepatic glutathione concentration. On the other hand, administration of silymarin resulted in an elevation of hepatic superoxide dismutase levels. Moreover, both Sm and silymarin treatment inhibited the elevation of hepatic inducible nitric oxide (iNOS) protein content and nitrite concentration in liver homogenate 24 h after CCl4 intoxication. We concluded that administration of Sm is effective in amelioration of CCl4-induced hepatotoxicity. This effect may be due to its ability to decrease the metabolic activation Of CCl4 by an increase in P450 2E1 protein content and its antioxidant activity associated with less increase in hepatic NOS protein content.
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页码:202 / 210
页数:9
相关论文
共 40 条
[1]  
AEBI H, 1984, METHOD ENZYMOL, V105, P121
[2]  
Al-Shabanah OA, 1999, LIFE SCI, V66, P265
[3]   Interleukin-1 and nitric oxide protect against tumor necrosis factor alpha-induced liver injury through distinct pathways [J].
Bohlinger, I ;
Leist, M ;
Barsig, J ;
Uhlig, S ;
Tiegs, G ;
Wendel, A .
HEPATOLOGY, 1995, 22 (06) :1829-1837
[4]   Silymarin retards collagen accumulation in early and advanced biliary fibrosis secondary to complete bile duct obliteration in rats [J].
Boigk, G ;
Stroedter, L ;
Herbst, H ;
Waldschmidt, J ;
Riecken, EO ;
Schuppan, D .
HEPATOLOGY, 1997, 26 (03) :643-649
[5]   Reduction of carbon tetrachloride-induced rat liver injury by IRFI 042, a novel dual vitamin E-like antioxidant [J].
Campo, GM ;
Squadrito, F ;
Ceccarelli, S ;
Calò, M ;
Avenoso, A ;
Campo, S ;
Squadrito, G ;
Altavilla, D .
FREE RADICAL RESEARCH, 2001, 34 (04) :379-+
[6]   TUMOR-NECROSIS-FACTOR-ALPHA AND NITRIC-OXIDE PRODUCTION IN ENDOTOXIN-PRIMED RATS ADMINISTERED CARBON-TETRACHLORIDE [J].
CHAMULITRAT, W ;
BLAZKA, ME ;
JORDAN, SJ ;
LUSTER, MI ;
MASON, RP .
LIFE SCIENCES, 1995, 57 (24) :2273-2280
[7]  
CHEN WZ, 1984, ACTA PHARM SIN, V19, P876
[8]  
CONNOR HD, 1990, MOL PHARMACOL, V37, P443
[9]   PREVENTION OF CARBON TETRACHLORIDE-INDUCED RAT-LIVER INJURY BY SOLUBLE TUMOR-NECROSIS-FACTOR RECEPTOR [J].
CZAJA, MJ ;
XU, J ;
ALT, E .
GASTROENTEROLOGY, 1995, 108 (06) :1849-1854
[10]   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