Effect of Sho-saiko-to extract on hepatic inflammation and fibrosis in dimethylnitrosamine induced liver injury rats

被引:48
作者
Kusunose, M [1 ]
Qiu, B [1 ]
Cui, TL [1 ]
Hamada, A [1 ]
Yoshioka, S [1 ]
Ono, M [1 ]
Miyamura, M [1 ]
Kyotani, S [1 ]
Nishioka, Y [1 ]
机构
[1] Kochi Med Sch Hosp, Dept Pharm, Nanko Ku, Kochi 7838505, Japan
关键词
Sho-saiko-to; liver fibrosis; dimethylnitrosamine; retinoid; TGF-beta; hydroxyproline;
D O I
10.1248/bpb.25.1417
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
Sho-saiko-to extract, a Chinese herbal medicine, is widely used for treatment of chronic hepatitis in Japan. However, it is not clear what conditions Sho-saiko-to extract improves hepatic inflammation and fibrosis. We therefore induced various stages of liver injury in model rats and administered Sho-saiko-to extract. We then evaluated the liver inflammation and liver fibrosis-improving effects of Sho-saiko-to extract. The liver injury model rats were produced by administration of various doses of dimethylnitrosamine (DMN) and Sho-saiko-to extract was administered to these rats. Then the liver inflammation and fibrosis-improving effects of Sho-saiko-to extract were evaluated according to L-asparate aminotransferase (AST), L-alanine aminotransferase (ALT), liver retinoid levels, levels of hydroxyproline, Transforming Growth Factor-beta (TGF-beta), and the liver fibrosis area. These indicators depended on the total doses of DMN. The ability of Sho-saiko-to extract to improve liver inflammation and fibrosis was limited to the following levels of the respective parameters: AST levels (234-264 U/l), ALT levels (208-232 U/l), TGF-beta levels (1102-1265 pg/g liver tissue), hydroxyproline levels (633-719 nmol/g liver tissue), and liver fibrosis area (9.7-10.6 times for normal rat). These findings suggested that Sho-saiko-to extract is effective in the treatment of liver inflammation and fibrosis up to a certain degree of severity, but it produces no improvement in more severe cases.
引用
收藏
页码:1417 / 1421
页数:5
相关论文
共 29 条
[1]
Baroni GS, 1996, HEPATOLOGY, V23, P1189
[2]
ELECTRON-MICROSCOPE STUDY OF PRODUCTION OF ASCITES IN ACUTE DIMETHYLNITROSAMINE (DMN)-INDUCED LIVER INJURY [J].
BHATHAL, PS ;
HURLEY, JV .
JOURNAL OF PATHOLOGY, 1973, 111 (02) :103-&
[3]
DEGAWA M, 1995, YAKUGAKU ZASSHI, V115, P1
[4]
INTRAVASCULAR COAGULATION IN ACUTE LIVER-FAILURE IN RATS AND ITS TREATMENT WITH ANTITHROMBIN-III [J].
FUJIWARA, K ;
OGATA, I ;
OHTA, Y ;
HIRATA, K ;
OKA, Y ;
YAMADA, S ;
SATO, Y ;
MASAKI, N ;
OKA, H .
GUT, 1988, 29 (08) :1103-1108
[5]
Dimethylnitrosamine-induced liver injury in rats: the early deposition of collagen [J].
George, J ;
Rao, KR ;
Stern, R ;
Chandrakasan, G .
TOXICOLOGY, 2001, 156 (2-3) :129-138
[6]
Biochemical abnormalities during the progression of hepatic fibrosis induced by dimethylnitrosamine [J].
George, J ;
Chandrakasan, G .
CLINICAL BIOCHEMISTRY, 2000, 33 (07) :563-570
[7]
FURTHER-STUDIES ON DIMETHYLNITROSAMINE METABOLISM, ACTIVATION AND ITS ABILITY TO CAUSE LIVER-INJURY [J].
GOMEZ, MID ;
GODOY, HM ;
CASTRO, JA .
ARCHIVES OF TOXICOLOGY, 1981, 47 (03) :159-168
[8]
HEPATIC SINUSOIDAL CELL DESTRUCTION IN THE DEVELOPMENT OF INTRAVASCULAR COAGULATION IN ACUTE LIVER-FAILURE OF RATS [J].
HIRATA, K ;
OGATA, I ;
OHTA, Y ;
FUJIWARA, K .
JOURNAL OF PATHOLOGY, 1989, 158 (02) :157-165
[9]
9,13-di-cis-retinoic acid induces the production of tPA and activation of latent TGF-beta via RAR alpha in a human liver stellate cell line, LI90 [J].
Imai, S ;
Okuno, M ;
Moriwaki, H ;
Muto, Y ;
Murakami, K ;
Shudo, K ;
Suzuki, Y ;
Kojima, S .
FEBS LETTERS, 1997, 411 (01) :102-106
[10]
EFFECTS OF VENTROMEDIAL AND LATERAL HYPOTHALAMIC-STIMULATION ON CHEMICALLY-INDUCED LIVER-INJURY IN RATS [J].
IWAI, M ;
SHIMAZU, T .
LIFE SCIENCES, 1988, 42 (19) :1833-1840