Document Detail


Down-regulation of liver Galbeta1, 4GlcNAc alpha2, 6-sialyltransferase gene by ethanol significantly correlates with alcoholic steatosis in humans.
MedLine Citation:
PMID:  19013288     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Hepatic steatosis and steatohepatitis are frequent results of long-term ethanol exposure. We have previously demonstrated that long-term ethanol down-regulates Galbetal, 4GlcNAc alpha2, 6-sialyltransferase (ST6Gal1), leading to defective glycosylation of a number of proteins including apolipoprotein (apo) E and apo J and the appearance of asialoconjugates in the blood of continuously alcohol-fed animals as well as in human alcoholics. In the current study, we have explored the possibility of whether ethanol-induced down-regulation of ST6Gal1 could contribute toward alcoholic steatosis in human alcoholics presumably because of impaired lipid and lipoprotein transport caused by this down-regulation. Real-time quantitative polymerase chain reaction analyses of liver samples from nondrinkers, moderate drinkers, and heavy drinkers as well as from subjects with and without alcoholic liver disease revealed direct evidence that the down-regulation of ST6Gal1 may be due to ethanol per se. The ST6Gal1 messenger RNA level was reduced by as much as 70% in moderate and heavy drinkers as well as in patients with alcoholic liver disease, but was not changed in subjects with liver disease due to causes other than alcohol exposure. Biochemical and histopathologic analysis demonstrated that the liver total cholesterol was increased by more than 30% (P < .05) and 75% (P < .01), respectively, in moderate and heavy drinkers compared with nondrinkers, with even more dramatic changes in triglyceride levels. Significantly, there was a strong inverse correlation between ST6Gal1 messenger RNA level and liver lipid deposit (F = 8.68, P < .001) by statistical analysis. Thus, it is suggested that alcohol-mediated down-regulation of hepatic ST6Gal1 gene leads to defective glycosylation of lipid-carrying apolipoproteins such as apo E and apo J, resulting in defective intracellular lipid and lipoprotein transport, which in turn may contribute to alcoholic steatosis.
Authors:
Maokai Gong; Leslie Castillo; Robert S Redman; Mamatha Garige; Kenneth Hirsch; Magnus Azuine; Richard L Amdur; Devanshi Seth; Paul S Haber; M Raj Lakshman
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Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural    
Journal Detail:
Title:  Metabolism: clinical and experimental     Volume:  57     ISSN:  1532-8600     ISO Abbreviation:  Metab. Clin. Exp.     Publication Date:  2008 Dec 
Date Detail:
Created Date:  2008-11-17     Completed Date:  2008-12-09     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  0375267     Medline TA:  Metabolism     Country:  United States    
Other Details:
Languages:  eng     Pagination:  1663-8     Citation Subset:  IM    
Affiliation:
The Lipid Research Laboratory, Veterans Affairs Medical Center, The George Washington University, Washington, DC 20422, USA.
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MeSH Terms
Descriptor/Qualifier:
Adult
Aged
Alcohol Drinking / metabolism
Down-Regulation / drug effects*
Ethanol / pharmacology
Fatty Liver, Alcoholic / genetics*,  metabolism,  pathology
Gene Expression Regulation, Enzymologic / drug effects
Humans
Lipid Metabolism / drug effects
Lipoproteins / metabolism
Liver / drug effects*,  enzymology,  metabolism
Middle Aged
RNA, Messenger / metabolism
Sialyltransferases / genetics*,  metabolism
Young Adult
Grant Support
ID/Acronym/Agency:
R01 AA08149/AA/NIAAA NIH HHS
Chemical
Reg. No./Substance:
0/Lipoproteins; 0/RNA, Messenger; 64-17-5/Ethanol; EC 2.4.99.-/Sialyltransferases; EC 2.4.99.-/galactosyl-1-3-N-acetylgalactosaminyl-specific 2,6-sialyltransferase

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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