Prostaglandins and cannabis--XVI. Antagonism of delta 1-tetrahydrocannabinol action by its metabolites

Biochem Pharmacol. 1986 Aug 1;35(15):2553-8. doi: 10.1016/0006-2952(86)90053-5.

Abstract

Prior exposure of cells in vitro to delta 1-tetrahydrocannabinol-7-oic acid (delta 1-THC-7-oic acid) reduced the degree of stimulation of prostaglandin synthesis incurred by subsequent treatment with delta 1-THC. The site of action of this inhibitory effect seemed to be on cyclooxygenase and not at the earlier step involving the phospholipase-mediated release of arachidonic acid. delta 1-THC-7-oic acid is a major metabolite of delta 1-THC and has no psychoactivity in humans. Our findings raise the possibility, however, that it may influence the in vivo activities of delta 1-THC by antagonizing its stimulatory action on cellular prostaglandin synthesis.

Publication types

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

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / pharmacology
  • Arachidonic Acid
  • Arachidonic Acids / metabolism
  • Cyclooxygenase Inhibitors
  • Dinoprostone
  • Dronabinol / analogs & derivatives*
  • Dronabinol / antagonists & inhibitors*
  • Dronabinol / metabolism
  • Dronabinol / pharmacology
  • Humans
  • Mice
  • Mice, Inbred Strains
  • Prostaglandins E / biosynthesis
  • Thromboxanes / biosynthesis

Substances

  • Anti-Inflammatory Agents
  • Arachidonic Acids
  • Cyclooxygenase Inhibitors
  • Prostaglandins E
  • Thromboxanes
  • Arachidonic Acid
  • 11-nor-delta(9)-tetrahydrocannabinol-9-carboxylic acid
  • Dronabinol
  • Dinoprostone