Literature DB >> 19170665

Chronic ethanol feeding alters hepatocyte memory which is not altered by acute feeding.

F Bardag-Gorce1, Joan Oliva, Jennifer Dedes, Jun Li, Barbara A French, Samuel W French.   

Abstract

BACKGROUND: Gene expression changes in the liver after acute binge drinking may differ from the changes seen in chronic ethanol feeding in the rat. The changes in gene expression after chronic ethanol feeding may sensitize the liver to alcohol-induced liver damage, which is not seen after acute binge drinking.
METHODS: To test this hypothesis, gene microarray analysis was performed on the livers of rats (n = 3) fed an acute binge dose of ethanol (6 g/kg body wt) and killed at 3 and 12 hours after ethanol by gavage. The gene microarrays were compared with those made on the liver of rats from a previous study, in which the rats were fed ethanol by intragastric tube for 1 month (36% of calories derived from ethanol).
RESULTS: Microarray analysis data varied between the acute and chronic models in several important respects. Growth factors increased mainly in the chronic alcohol fed rat. Changes in enzymes involved in oxidative stress were noted only with chronic ethanol feeding. Gene expression of fat metabolism was increased only with chronic ethanol feeding. Most importantly, epigenetic related enzymes and acetylation and methylation of histones changed only after chronic ethanol feeding.
CONCLUSIONS: The results support the concept that chronic ethanol ingestion induces altered gene expression as a result of changes in epigenetic mechanisms, where acetylation and methylation of histones were altered.

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Year:  2009        PMID: 19170665      PMCID: PMC2811268          DOI: 10.1111/j.1530-0277.2008.00885.x

Source DB:  PubMed          Journal:  Alcohol Clin Exp Res        ISSN: 0145-6008            Impact factor:   3.455


  17 in total

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Journal:  Exp Mol Pathol       Date:  2006-10-10       Impact factor: 3.362

7.  Mechanism of the alcohol cyclic pattern: role of the hypothalamic-pituitary-thyroid axis.

Authors:  J Li; V Nguyen; B A French; A F Parlow; G L Su; P Fu; Q X Yuan; S W French
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8.  Liver hypoxia and lack of recovery after reperfusion at high blood alcohol levels in the intragastric feeding model of alcohol liver disease.

Authors:  Jun Li; Barbara French; Yong Wu; Ravi Vanketesh; Rosalyn Montgomery; Fawzia Bardag-Gorce; Jennifer Kitto; Samuel W French
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9.  The importance of cycling of blood alcohol levels in the pathogenesis of experimental alcoholic liver disease in rats.

Authors:  Fawzia Bardag-Gorce; Barbara A French; Jun Li; Nora E Riley; Qi X Yuan; Vimonrat Valinluck; Paul Fu; Magnus Ingelman-Sundberg; Seokjoo Yoon; Samuel W French
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  22 in total

Review 1.  Histone modifications and alcohol-induced liver disease: are altered nutrients the missing link?

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3.  Gene-selective histone H3 acetylation in the absence of increase in global histone acetylation in liver of rats chronically fed alcohol.

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6.  Epigenetic regulation of hepatic endoplasmic reticulum stress pathways in the ethanol-fed cystathionine beta synthase-deficient mouse.

Authors:  Farah Esfandiari; Valentina Medici; Donna H Wong; Soumia Jose; Maryam Dolatshahi; Eoin Quinlivan; Sanjana Dayal; Steven R Lentz; Hidekazu Tsukamoto; Yue Hua Zhang; Samuel W French; Charles H Halsted
Journal:  Hepatology       Date:  2010-03       Impact factor: 17.425

7.  Gene expression modifications in the liver caused by binge drinking and S-adenosylmethionine feeding. The role of epigenetic changes.

Authors:  Jun Li; Fawzia Bardag-Gorce; Joan Oliva; Jennifer Dedes; Barbara A French; Samuel W French
Journal:  Genes Nutr       Date:  2009-12-04       Impact factor: 5.523

8.  The effects of betaine treatment on rats fed an acute bolus of ethanol at 3 and 12 h post bolus: a microarray analysis.

Authors:  J Li; F Bardag-Gorce; J Oliva; B A French; J Dedes; S W French
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Review 9.  How to prevent alcoholic liver disease.

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