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10.3748/wjg.v19.i19.2921

http://scihub22266oqcxt.onion/10.3748/wjg.v19.i19.2921
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suck abstract from ncbi


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pmid23704825      World+J+Gastroenterol 2013 ; 19 (19): 2921-34
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  • Inhibiting heme oxygenase-1 attenuates rat liver fibrosis by removing iron accumulation #MMPMID23704825
  • Wang QM; Du JL; Duan ZJ; Guo SB; Sun XY; Liu Z
  • World J Gastroenterol 2013[May]; 19 (19): 2921-34 PMID23704825show ga
  • AIM: To investigate the effects of the heme oxygenase (HO)-1/carbon monoxide system on iron deposition and portal pressure in rats with hepatic fibrosis induced by bile duct ligation (BDL). METHODS: Male Sprague-Dawley rats were divided randomly into a Sham group, BDL group, Fe group, deferoxamine (DFX) group, zinc protoporphyrin (ZnPP) group and cobalt protoporphyrin (CoPP) group. The levels of HO-1 were detected using different methods. The serum carboxyhemoglobin (COHb), iron, and portal vein pressure (PVP) were also quantified. The plasma and mRNA levels of hepcidin were measured. Hepatic fibrosis and its main pathway were assessed using Van Gieson's stain, hydroxyproline, transforming growth factor-beta1 (TGF-beta1), nuclear factor-E2-related factor 2 (Nrf2), matrix metalloproteinase-2 (MMP-2) and tissue inhibitor of metalloproteinase-1 (TIMP-1). RESULTS: Serum COHb and protein and mRNA expression levels of HO-1 and Nrf2 were increased in the BDL group compared with the Sham group and were much higher in the CoPP group. The ZnPP group showed lower expression of HO-1 and Nrf2 and lower COHb. The levels of iron and PVP were enhanced in the BDL group but were lower in the ZnPP and DFX groups and were higher in the CoPP and Fe groups. Hepcidin levels were higher, whereas superoxide dismutase levels were increased and malonaldehyde levels were decreased in the ZnPP and DFX groups. The ZnPP group also showed inhibited TGF-beta1 expression and regulated TIMP-1/MMP-2 expression, as well as obviously attenuated liver fibrosis. CONCLUSION: Reducing hepatic iron deposition and CO levels by inhibiting HO-1 activity though the Nrf2/Keap pathway could be helpful in improving hepatic fibrosis and regulating PVP.
  • |Animals[MESH]
  • |Carbon Dioxide/metabolism[MESH]
  • |Carboxyhemoglobin/metabolism[MESH]
  • |Enzyme Inhibitors/*pharmacology[MESH]
  • |Heme Oxygenase (Decyclizing)/*antagonists & inhibitors/biosynthesis/genetics/metabolism[MESH]
  • |Hepcidins/blood[MESH]
  • |Iron/*blood[MESH]
  • |Liver Cirrhosis, Experimental/enzymology/pathology/physiopathology/*prevention & control[MESH]
  • |Liver/*drug effects/enzymology/pathology[MESH]
  • |Male[MESH]
  • |Malondialdehyde/metabolism[MESH]
  • |Matrix Metalloproteinase 2/metabolism[MESH]
  • |NF-E2-Related Factor 2/metabolism[MESH]
  • |Oxidative Stress/drug effects[MESH]
  • |Portal Pressure/drug effects[MESH]
  • |Protoporphyrins/*pharmacology[MESH]
  • |RNA, Messenger/blood[MESH]
  • |Rats[MESH]
  • |Rats, Sprague-Dawley[MESH]
  • |Superoxide Dismutase/metabolism[MESH]
  • |Time Factors[MESH]
  • |Tissue Inhibitor of Metalloproteinase-1/metabolism[MESH]


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