Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
12
pubmed:dateCreated
2010-11-29
pubmed:abstractText
In nonalcoholic fatty liver disease (NAFLD), depletion of hepatic antioxidants may contribute to the progression of steatosis to nonalcoholic steatohepatitis (NASH) by increasing oxidative stress that produces lipid peroxidation, inflammation, and fibrosis. We investigated whether depletion of glutathione (GSH) increases NASH-associated hepatic pathology in mice fed a diet deficient in methionine and choline (MCD diet). Wild-type (wt) mice and genetically GSH-deficient mice lacking the modifier subunit of glutamate cysteine ligase (Gclm null mice), the rate-limiting enzyme for de novo synthesis of GSH, were fed the MCD diet, a methionine/choline-sufficient diet, or standard chow for 21 days. We assessed NASH-associated hepatic pathology, including steatosis, fibrosis, inflammation, and hepatocyte ballooning, and used the NAFLD Scoring System to evaluate the extent of changes. We measured triglyceride levels, determined the level of lipid peroxidation products, and measured by qPCR the expression of mRNAs for several proteins associated with lipid metabolism, oxidative stress, and fibrosis. MCD-fed GSH-deficient Gclm null mice were to a large extent protected from MCD diet-induced excessive fat accumulation, hepatocyte injury, inflammation, and fibrosis. Compared with wt animals, MCD-fed Gclm null mice had much lower levels of F?-isoprostanes, lower expression of acyl-CoA oxidase, carnitine palmitoyltransferase 1a, uncoupling protein-2, stearoyl-coenzyme A desaturase-1, transforming growth factor-?, and plasminogen activator inhibitor-1 mRNAs, and higher activity of catalase, indicative of low oxidative stress, inhibition of triglyceride synthesis, and lower expression of profibrotic proteins. Global gene analysis of hepatic RNA showed that compared with wt mice, the livers of Gclm null mice have a high capacity to metabolize endogenous and exogenous compounds, have lower levels of lipogenic proteins, and increased antioxidant activity. Thus, metabolic adaptations resulting from severe GSH deficiency seem to protect against the development of steatohepatitis.
pubmed:grant
http://linkedlifedata.com/resource/pubmed/grant/P30 ES007033-15, http://linkedlifedata.com/resource/pubmed/grant/P30ES07033, http://linkedlifedata.com/resource/pubmed/grant/R01 CA074131-08, http://linkedlifedata.com/resource/pubmed/grant/R01 CA127228-02, http://linkedlifedata.com/resource/pubmed/grant/R01 ES010849-02, http://linkedlifedata.com/resource/pubmed/grant/R01CA074131, http://linkedlifedata.com/resource/pubmed/grant/R01CA127228, http://linkedlifedata.com/resource/pubmed/grant/R01ES10849, http://linkedlifedata.com/resource/pubmed/grant/R37 CA023226-34, http://linkedlifedata.com/resource/pubmed/grant/R37CA023226, http://linkedlifedata.com/resource/pubmed/grant/T32 ES007032-33, http://linkedlifedata.com/resource/pubmed/grant/T32 ES007032-34, http://linkedlifedata.com/resource/pubmed/grant/T32ES007032, http://linkedlifedata.com/resource/pubmed/grant/U19 ES011387-06, http://linkedlifedata.com/resource/pubmed/grant/U19ES011387
pubmed:commentsCorrections
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pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
1530-0307
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
90
pubmed:owner
NLM
pubmed:authorsComplete
Y
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