TNF-α and leptin in experimental liver fibrosis models induced by carbon tetrachloride and by common bile duct ligation

被引:22
作者
Bahçecioglu, IH
Yalniz, M
Ataseven, H
Bülbüller, N
Keçeci, M
Demirdag, K
Özercan, I
Üstündag, B
机构
[1] Firat Univ, Fac Med, Dept Gastroenterol, Elazig, Turkey
[2] Firat Univ, Fac Med, Dept Internal Med, Elazig, Turkey
[3] Firat Univ, Fac Med, Dept Gen Surg, Elazig, Turkey
[4] Firat Univ, Fac Med, Dept Infect Dis, Elazig, Turkey
[5] Firat Univ, Fac Med, Dept Pathol, Elazig, Turkey
[6] Firat Univ, Fac Med, Dept Biochem, Elazig, Turkey
关键词
carbon tetrachloride; common bile duct ligation; liver fibrosis; leptin; TNF-alpha;
D O I
10.1002/cbf.1114
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
In this study we investigated TNF-alpha and leptin levels in two different liver fibrosis models induced by carbon tetrachloride (CCl4) and common bile duct ligation (CBDL). A total of 36 male rats of Albino-Wistar strain were allocated to three groups. One of the groups was the control. The second group received 0.15 ml 100 g(-1) CCl4 subcutaneously for 6 weeks, 3 days per week. The third group underwent common bile duct ligation (CBDL) and was monitored for 4 weeks. Histopathological investigation included fibrosis, steatosis and inflammation. Serum IL-6 and TNF-alpha levels were analysed by ELISA methods and leptin was analysed by RIA. Fibrosis and steatosis increased significantly in the CCl4 group in comparison with the CBDL group (p < 0.0 1; p < 0.001). Leptin and TNF-alpha levels in CCl4 group were higher than those in the CBDL and control groups (p < 0.05). TNF-alpha and leptin levels were not related to each another in either the CCl4 group or the CBDL cup (r = 0.22 p > 0.05; r = 0.19, p > 0.05). The IL-6 level was higher in the CCl4 group in relation to severity of inflammation (p < 0.05). TNF-alpha and leptin levels were higher in animals with liver fibrosis induced by CCl4, than they were in those whose liver fibrosis was induced by common bile duct ligation. Leptin and TNF-alpha may be less effective on the development of liver fibrosis in the group which underwent common bile duct ligation. Copyright (C) 2004 John Wiley Sons, Ltd.
引用
收藏
页码:359 / 363
页数:5
相关论文
共 32 条
[1]
Polyenylphosphatidylcholine prevents carbon tetrachloride-induced lipid peroxidation while it attenuates liver fibrosis [J].
Aleynik, SI ;
Leo, MA ;
Ma, XL ;
Aleynik, MK ;
Lieber, CS .
JOURNAL OF HEPATOLOGY, 1997, 27 (03) :554-561
[2]
Leptin [J].
Auwerx, J ;
Staels, B .
LANCET, 1998, 351 (9104) :737-742
[3]
BEYAERT R, 1996, NEW ENGL J MED, V334, P1717
[4]
BRATTIN W J, 1985, Journal of Free Radicals in Biology and Medicine, V1, P27, DOI 10.1016/0748-5514(85)90026-1
[5]
Induction of early-immediate genes by tumor necrosis factor alpha contribute to liver repair following chemical-induced hepatotoxicity [J].
Bruccoleri, A ;
Gallucci, R ;
Germolec, DR ;
Blackshear, P ;
Simeonova, P ;
Thurman, RG ;
Luster, MI .
HEPATOLOGY, 1997, 25 (01) :133-141
[6]
Modulation of insulin activities by leptin [J].
Cohen, B ;
Novick, D ;
Rubinstein, M .
SCIENCE, 1996, 274 (5290) :1185-1188
[7]
Liver failure and defective hepatocyte regeneration in interleukin-6-deficient mice [J].
Cressman, DE ;
Greenbaum, LE ;
DeAngelis, RA ;
Ciliberto, G ;
Furth, EE ;
Poli, V ;
Taub, R .
SCIENCE, 1996, 274 (5291) :1379-1383
[8]
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
[9]
Cytokine regulation of liver injury and repair [J].
Diehl, AM .
IMMUNOLOGICAL REVIEWS, 2000, 174 :160-171
[10]
NF-kappa B activation and modulation in hepatic macrophages during cholestatic injury [J].
Fox, ES ;
Kim, JC ;
Tracy, TF .
JOURNAL OF SURGICAL RESEARCH, 1997, 72 (02) :129-134