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10.1053/j.gastro.2008.01.011

http://scihub22266oqcxt.onion/10.1053/j.gastro.2008.01.011
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suck abstract from ncbi

pmid18395094      Gastroenterology 2008 ; 134 (4): 1159-68
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  • Nuclear factor-eythroid 2-related factor 2 prevents alcohol-induced fulminant liver injury #MMPMID18395094
  • Lamle J; Marhenke S; Borlak J; von Wasielewski R; Eriksson CJ; Geffers R; Manns MP; Yamamoto M; Vogel A
  • Gastroenterology 2008[Apr]; 134 (4): 1159-68 PMID18395094show ga
  • BACKGROUND & AIMS: The transcription factor nuclear factor-eythroid 2-related factor 2 (Nrf2(-/-)) is essential for protecting cells against xenobiotic and oxidative stress. Increased oxidative stress has been implicated in the pathophysiology of many diseases including ethanol-induced liver disease. Therefore, the role of Nrf2(-/-) in ethanol-induced liver injury was investigated. METHODS: Wild-type and Nrf2(-/-) mice were fed with the ethanol diet, followed by examination of liver pathology, mortality, and ethanol metabolism. RESULTS: Nrf2(-/-) mice displayed a dramatically increased mortality associated with liver failure when fed doses of ethanol that were tolerated by WT mice. Nrf2(-/-) mice showed a significantly reduced ability to detoxify acetaldehyde, leading to an accumulation of the toxic metabolite. Loss of Nrf2(-/-) caused a marked steatosis in livers of ethanol-fed mice, and Srebp1 was identified as a candidate transcription factor responsible for lipogenic enzyme induction. Furthermore, ethanol consumption led to a progressive depletion of total and mitochondrial reduced glutathione, which was associated with more pronounced structural and functional changes to mitochondria of Nrf2(-/-) mice. In addition, ethanol feeding elicited an aggravated inflammatory response mediated by Kupffer cells in Nrf2(-/-) mice as shown by an increased tumor necrosis factor-alpha secretion and activation of the interleukin-6/Stat-3 pathway. Together these changes lead to a vicious cycle of accumulating hepatocellular damage, ultimately leading to liver failure and death of Nrf2(-/-) mice. CONCLUSIONS: Our data establish a central role for Nrf2(-/-) in the protection against ethanol-induced liver injury.
  • |Aldehyde Dehydrogenase 1 Family[MESH]
  • |Aldehyde Dehydrogenase/metabolism[MESH]
  • |Animals[MESH]
  • |Blotting, Western[MESH]
  • |Central Nervous System Depressants/toxicity[MESH]
  • |Chromatography, High Pressure Liquid[MESH]
  • |Electrophoresis, Polyacrylamide Gel[MESH]
  • |Enzyme-Linked Immunosorbent Assay[MESH]
  • |Ethanol/toxicity[MESH]
  • |Follow-Up Studies[MESH]
  • |Gene Expression[MESH]
  • |Immunohistochemistry[MESH]
  • |In Situ Nick-End Labeling[MESH]
  • |Isoenzymes[MESH]
  • |Liver Cirrhosis, Alcoholic/*complications/metabolism/pathology[MESH]
  • |Liver Cirrhosis, Experimental/*complications/metabolism/pathology[MESH]
  • |Liver Failure, Acute/etiology/metabolism/*prevention & control[MESH]
  • |Liver/drug effects/metabolism/pathology[MESH]
  • |Male[MESH]
  • |Mice[MESH]
  • |Mice, Inbred C57BL[MESH]
  • |NF-E2-Related Factor 2/*therapeutic use[MESH]
  • |Oxidative Stress[MESH]
  • |RNA/genetics[MESH]
  • |Retinal Dehydrogenase[MESH]
  • |Reverse Transcriptase Polymerase Chain Reaction[MESH]
  • |Sterol Regulatory Element Binding Protein 1/biosynthesis/genetics[MESH]


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