Skip to main content
eScholarship
Open Access Publications from the University of California

Antidepressant-like activity and modulation of brain monoaminergic transmission by blockade of anandamide hydrolysis.

  • Author(s): Gobbi, G
  • Bambico, FR
  • Mangieri, R
  • Bortolato, M
  • Campolongo, P
  • Solinas, M
  • Cassano, T
  • Morgese, MG
  • Debonnel, G
  • Duranti, A
  • Tontini, A
  • Tarzia, G
  • Mor, M
  • Trezza, V
  • Goldberg, SR
  • Cuomo, V
  • Piomelli, D
  • et al.
Abstract

Although anecdotal reports suggest that cannabis may be used to alleviate symptoms of depression, the psychotropic effects and abuse liability of this drug prevent its therapeutic application. The active constituent of cannabis, delta9-tetrahydrocannabinol, acts by binding to brain CB1 cannabinoid receptors, but an alternative approach might be to develop agents that amplify the actions of endogenous cannabinoids by blocking their deactivation. Here, we show that URB597, a selective inhibitor of the enzyme fatty-acid amide hydrolase, which catalyzes the intracellular hydrolysis of the endocannabinoid anandamide, exerts potent antidepressant-like effects in the mouse tail-suspension test and the rat forced-swim test. Moreover, URB597 increases firing activity of serotonergic neurons in the dorsal raphe nucleus and noradrenergic neurons in the nucleus locus ceruleus. These actions are prevented by the CB1 antagonist rimonabant, are accompanied by increased brain anandamide levels, and are maintained upon repeated URB597 administration. Unlike direct CB1 agonists, URB597 does not exert rewarding effects in the conditioned place preference test or produce generalization to the discriminative effects of delta9-tetrahydrocannabinol in rats. The findings support a role for anandamide in mood regulation and point to fatty-acid amide hydrolase as a previously uncharacterized target for antidepressant drugs.

Many UC-authored scholarly publications are freely available on this site because of the UC's open access policies. Let us know how this access is important for you.

Main Content
Current View