Localization of drug-metabolizing enzyme activities to blood-brain interfaces and circumventricular organs

J Neurochem. 1994 Mar;62(3):1089-96. doi: 10.1046/j.1471-4159.1994.62031089.x.

Abstract

The brain, with the exception of the choroid plexuses and circumventricular organs, is partially protected from the invasion of blood-borne chemicals by the specific morphological properties of the cerebral micro-vessels, namely, the tight junctions of the blood-brain barrier. Recently, several enzymes that are primarily involved in hepatic drug metabolism have been shown to exist in the brain, albeit at relatively low specific activities. In the present study, the hypothesis that these enzymes are located primarily at blood-brain interfaces, where they form an "enzymatic barrier," is tested. By using microdissection techniques or a gradient-centrifugation isolation procedure, the activities of seven drug-metabolizing enzymes in isolated microvessels, choroid plexuses, meningeal membranes, and tissue from three circumventricular organs (the neural lobe of the hypophysis, pineal gland, and median eminence) were assayed. With two exceptions, the activities of these enzymes were higher in the three circumventricular organs and cerebral microvessel than in the cortex. Very high membrane-bound epoxide hydrolase and UDP-glucuronosyltransferase activities (approaching those in liver) and somewhat high 7-benzoxyresorufin-O-dealkylase and NADPH-cytochrome P-450 reductase activities were determined in the choroid plexuses. The pia-arachnoid membranes, but not the dura matter, displayed drug-metabolizing enzyme activities, notably that of epoxide hydrolase. The drug-metabolizing enzymes located at these nonparenchymal sites may function to protect brain tissue from harmful compounds.

MeSH terms

  • Animals
  • Blood-Brain Barrier*
  • Brain / enzymology*
  • Cerebral Ventricles
  • Choroid Plexus / enzymology
  • Cytochrome P-450 Enzyme System / metabolism
  • Epoxide Hydrolases / metabolism
  • Glucuronosyltransferase / metabolism
  • Isoenzymes / metabolism
  • Male
  • Pharmaceutical Preparations / metabolism*
  • Rats
  • Rats, Sprague-Dawley
  • Tissue Distribution

Substances

  • Isoenzymes
  • Pharmaceutical Preparations
  • Cytochrome P-450 Enzyme System
  • Glucuronosyltransferase
  • Epoxide Hydrolases