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Journal of Pharmacology And Experimental Therapeutics Fast Forward
First published on July 7, 2006; DOI: 10.1124/jpet.106.108175


0022-3565/06/3191-360-368$20.00
JPET 319:360-368, 2006
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METABOLISM, TRANSPORT, AND PHARMACOGENOMICS

The Role of Retinoid X Receptor {alpha} in Regulating Alcohol Metabolism

Maxwell Afari Gyamfi, Michael George Kocsis, Lin He, Guoli Dai, Alphonse John Mendy, and Yu-Jui Yvonne Wan

Department of Pharmacology, Toxicology, and Therapeutics, University of Kansas Medical Center, Kansas City, Kansas

There is substantial overlap in retinol and alcohol metabolism. Mice that lack retinoic acid (RA) receptor retinoid X receptor {alpha} (RXR{alpha}) expression in the liver are more susceptible to alcoholic liver disease. To investigate the interaction between RXR{alpha} and alcoholic liver disease, ethanol metabolism was studied in hepatocyte RXR{alpha}-deficient [RXR{alpha} knockout (KO)] mice. Hepatocyte RXR{alpha} deficiency resulted in a significant increase in hepatic alcohol dehydrogenase (ADH) activity, ADH1 protein, but not Adh1 mRNA. Polysomal distribution analysis indicated that more polysome-associated Adh1 mRNA was present in the mutant mouse livers, suggesting increased ADH1 protein synthesis in RXR{alpha} KO mice compared with wild-type mice. However, ADH2 and ADH3 enzyme activities were not affected by RXR{alpha} deficiency. Although ethanol clearance was increased, acetaldehyde elimination was reduced when RXR{alpha} was not expressed in the liver. Both mitochondrial aldehyde dehydrogenase (ALDH) 2 and cytosolic ALDH activities were reduced in the mutant mice compared with the wild type. Western blot analysis revealed that the levels of ALDH1A1 and ALDH1A2 were decreased in the mutant mice. Semiquantitative reverse transcriptase-polymerase chain reaction indicated that liver Aldh1a1 mRNA level was also reduced due to the lack of RXR{alpha} expression. Thus, RXR{alpha} differentially affects ADH and ALDH activity, leading to an increase in alcohol clearance, but a reduction in acetaldehyde elimination. In addition, CYP2E1 as well as mitochondrial and cytosolic glutathione S-transferase activities were significantly lower in RXR{alpha} KO mice than in wild-type mice. Our results reveal the central role of RXR{alpha} in ethanol metabolism.


Received for publication May 20, 2006
Accepted July 6, 2006.

Address correspondence to: Dr. Yu-Jui Yvonne Wan, Department of Pharmacology, Toxicology, and Therapeutics, University of Kansas Medical Center, 3901 Rainbow Blvd., Kansas City, KS 66160-7417. E-mail: ywan{at}kumc.edu




This article has been cited by other articles:


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J. Pharmacol. Exp. Ther.Home page
M. A. Gyamfi, L. He, S. W. French, I. Damjanov, and Y.-J. Y. Wan
Hepatocyte Retinoid X Receptor {alpha}-Dependent Regulation of Lipid Homeostasis and Inflammatory Cytokine Expression Contributes to Alcohol-Induced Liver Injury
J. Pharmacol. Exp. Ther., February 1, 2008; 324(2): 443 - 453.
[Abstract] [Full Text] [PDF]




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