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10.1186/1476-511X-10-31

http://scihub22266oqcxt.onion/10.1186/1476-511X-10-31
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21314960!3048569!21314960
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suck abstract from ncbi

pmid21314960      Lipids+Health+Dis 2011 ; 10 (?): 31
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  • Induction of heme oxygenase-1 protects against nutritional fibrosing steatohepatitis in mice #MMPMID21314960
  • Wang RQ; Nan YM; Wu WJ; Kong LB; Han F; Zhao SX; Kong L; Yu J
  • Lipids Health Dis 2011[Feb]; 10 (?): 31 PMID21314960show ga
  • BACKGROUND: Heme oxygenase-1 (HO-1), an antioxidant defense enzyme, has been shown to protect against oxidant-induced liver injury. However, its role on liver fibrosis remains unclear. This study aims to elucidate the effect and the mechanism of HO-1 in nutritional fibrosing steatohepatitis in mice. METHODS: Male C57BL/6J mice were fed with a methionine-choline deficient (MCD) diet for eight weeks to induce hepatic fibrosis. HO-1 chemical inducer (hemin), HO-1 chemical inhibitor zinc protoporphyrin IX (ZnPP-IX) and/or adenovirus carrying HO-1 gene (Ad-HO-1) were administered to mice, respectively. Liver injury was assessed by serum ALT, AST levels and histological examination; hepatic lipid peroxides levels were determined; the expression levels of several fibrogenic related genes were assayed by real-time quantitative PCR and Western blot. RESULTS: MCD feeding mice showed progressive hepatic injury including hepatic steatosis, inflammatory infiltration and fibrosis. Induction of HO-1 by hemin or Ad-HO-1 significantly attenuated the severity of liver injury. This effect was associated with the up-regulation of HO-1, reduction of hepatic lipid peroxides levels, down-regulation of inflammatory factors tumor necrosis factor-alpha, interleukin-6 and suppressor of cytokine signaling-1 as well as the pro-fibrotic genes alpha-smooth muscle actin, transforming growth factor-beta1, matrix metallopeptidase-2 and matrix metallopeptidase-9. A contrary effect was observed in mice treated with ZnPP-IX. CONCLUSIONS: The present study provided the evidence for the protective role of HO-1 in ameliorating MCD diet-induced fibrosing steatohepatitis. Modulation of HO-1 expression might serve as a therapeutic approach for fibrotic steatohepatitis.
  • |Actins/biosynthesis[MESH]
  • |Alanine Transaminase/blood[MESH]
  • |Animals[MESH]
  • |Aspartate Aminotransferases/blood[MESH]
  • |Choline Deficiency/complications[MESH]
  • |Enzyme Induction[MESH]
  • |Fatty Liver/pathology/*prevention & control[MESH]
  • |Heme Oxygenase-1/*biosynthesis[MESH]
  • |Hemin/pharmacology[MESH]
  • |Lipid Peroxides/metabolism[MESH]
  • |Liver Cirrhosis/complications/etiology[MESH]
  • |Liver/drug effects/pathology[MESH]
  • |Male[MESH]
  • |Malondialdehyde/metabolism[MESH]
  • |Matrix Metalloproteinase 2/biosynthesis[MESH]
  • |Matrix Metalloproteinase 9/biosynthesis[MESH]
  • |Membrane Proteins/*biosynthesis[MESH]
  • |Methionine/deficiency[MESH]
  • |Mice[MESH]
  • |Mice, Inbred C57BL[MESH]
  • |Protoporphyrins/pharmacology[MESH]
  • |Transforming Growth Factor beta1/biosynthesis[MESH]
  • |Tumor Necrosis Factor-alpha/biosynthesis[MESH]


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