Expression, localization and potential physiological significance of alcohol dehydrogenase in the gastrointestinal tract

Eur J Biochem. 2003 Jun;270(12):2652-62. doi: 10.1046/j.1432-1033.2003.03642.x.


ADH1 and ADH4 are the major alcohol dehydrogenases (ADH) in ethanol and retinol oxidation. ADH activity and protein expression were investigated in rat gastrointestinal tissue homogenates by enzymatic and Western blot analyses. In addition, sections of adult rat gastrointestinal tract were examined by in situ hybridization and immunohistochemistry. ADH1 and ADH4 were detected along the whole tract, changing their localization and relative content as a function of the area studied. While ADH4 was more abundant in the upper (esophagus and stomach) and lower (colorectal) regions, ADH1 was predominant in the intestine but also present in stomach. Both enzymes were detected in mucosa but, in general, ADH4 was found in outer cell layers, lining the lumen, while ADH1 was detected in the inner cell layers. Of interest were the sharp discontinuities in the expression found in the pyloric region (ADH1) and the gastroduodenal junction (ADH4), reflecting functional changes. The precise localization of ADH in the gut reveals the cell types where active alcohol oxidation occurs during ethanol ingestion, providing a molecular basis for the gastrointestinal alcohol pathology. Localization of ADH, acting as retinol dehydrogenase/retinal reductase, also indicates sites of active retinoid metabolism in the gut, essential for mucosa function and vitamin A absorption.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Alcohol Dehydrogenase / genetics*
  • Alcohol Dehydrogenase / metabolism
  • Animals
  • Digestive System / enzymology*
  • Esophagus / enzymology
  • Ileum / enzymology
  • Immunohistochemistry
  • In Situ Hybridization
  • Intestinal Mucosa / enzymology*
  • Isoenzymes / genetics
  • Isoenzymes / metabolism
  • Jejunum / enzymology
  • Rats
  • Tongue / enzymology


  • Isoenzymes
  • Alcohol Dehydrogenase
  • alcohol dehydrogenase IV