Conversion of xanthine dehydrogenase to oxidase in ischemic rat intestine: a reevaluation

Am J Physiol. 1988 May;254(5 Pt 1):G768-74. doi: 10.1152/ajpgi.1988.254.5.G768.


Oxygen radicals derived from xanthine oxidase (XO) are important mediators of the cellular injury associated with reperfusion of ischemic intestine, stomach, liver, kidney, and pancreas. XO exists in nonischemic tissue predominantly as xanthine dehydrogenase (XDH) and converts to oxygen radical-producing XO with ischemia. Grinding intestine under liquid nitrogen and placing the powder in phosphate buffer (pH 7.0) containing thiol reductants and protease inhibitors adequately preserved total XDH + XO activity and the percentage in the oxidase form (%XO) for 24 h. Total activity in nonischemic intestine ranged from 374 nmol.min-1.g-1 in duodenum to 138 nmol.min-1.g-1 in ileum, while XO activity was approximately 19% of total activity throughout the entire small intestine. The rate of XDH conversion to XO during normothermic ischemia varied only slightly throughout the intestine, increasing 13% per hour to 34, 46, and 61% XO after 1, 2, and 3 h of ischemia, respectively. Our results contrast with previous reports where XDH conversion to XO occurred within 60 s ischemia but are consistent with physiological and morphological evidence of ischemic injury and provide further support for involvement of XO in intestinal injury associated with ischemia.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Dithiothreitol / pharmacology
  • Free Radicals
  • Hydrogen-Ion Concentration
  • Intestines / blood supply*
  • Intestines / enzymology
  • Ischemia / enzymology*
  • Ketone Oxidoreductases / metabolism*
  • Male
  • Protease Inhibitors / pharmacology
  • Rats
  • Rats, Inbred Strains
  • Xanthine Dehydrogenase / metabolism*
  • Xanthine Oxidase / metabolism*


  • Free Radicals
  • Protease Inhibitors
  • Xanthine Dehydrogenase
  • Xanthine Oxidase
  • Ketone Oxidoreductases
  • Dithiothreitol