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PMID: 9394122 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Regional restriction of alcohol/retinol dehydrogenases along the mouse gastrointestinal epithelium.

Alcoholism, clinical and experimental research ·Vol. 21 ·No. 8 ·1997-11-00 ·Pages 1484-90

Haselbeck RJ, Duester G

Abstract

The gastrointestinal tract is a major site of alcohol dehydrogenase (ADH) activity in humans and rodents. Because class I ADH (ADH-I) and class IV ADH (ADH-IV), but not class III ADH (ADH-III), function as retinol dehydrogenases in vitro and may thus participate in retinoid signaling needed for epithelial differentiation, the aim of this study was to determine the localization of these enzymes along the gastrointestinal tract. Specific antibodies were used to examine the tissue distribution of all three known classes of mouse ADH by Western blotting, and cellular localization was determined by immunohistochemistry. ADH-I was detected primarily in the intestine, liver, kidney, adrenal, and uterus, with detection of ADH-III in all tissues examined, and detection of ADH-IV primarily in the esophagus, stomach, adrenal, skin, ovary, and epididymis. Along the gastrointestinal tract, ADH-III was not specifically localized, whereas ADH-I was localized exclusively in the villus epithelium of the small intestine and absorptive epithelium of the large intestine, with ADH-IV being localized exclusively in the basal and suprabasal epithelial cells of the esophagus and gastric pit surface epithelium of the stomach. The ADH localization patterns observed are consistent with ADH-I and ADH-IV, but not ADH-III, functioning physiologically in retinol metabolism needed for epithelial differentiation. Our results further suggest that the functions of ADH-I and ADH-IV are regionally restricted to the lower and upper components, respectively, of the gastrointestinal epithelium, a finding that may relate to the different efficiencies of these two enzymes for retinol oxidation, as well as to the different susceptibilities of the upper and lower digestive tracts for ethanol-induced cancers.

MeSH Terms
Alcohol Dehydrogenase/metabolism Alcohol Oxidoreductases/metabolism Animals Blotting, Western Digestive System/enzymology Ethanol/pharmacokinetics,toxicity Gastric Mucosa/enzymology Immunoenzyme Techniques Intestinal Mucosa/enzymology Isoenzymes/metabolism Mice Vitamin A/metabolism
Chemicals
Isoenzymes Vitamin A Ethanol Alcohol Oxidoreductases Alcohol Dehydrogenase retinol dehydrogenase
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Haselbeck R J
Burnham Institute, La Jolla, CA 92037, USA.
Duester G
Article Info
Journal
Alcoholism, clinical and experimental research
Abbr.
Alcohol Clin Exp Res
ISSN
0145-6008
Published
1997-11-00
Pages
1484-90
Language
English
Region
England
NLM ID
7707242
Subset
IM
Grants
NIAAA NIH HHS · AA07261 · United States
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