Pregnenolone can protect the brain from cannabis intoxication. Academic Article uri icon

Overview

abstract

  • Pregnenolone is considered the inactive precursor of all steroid hormones, and its potential functional effects have been largely uninvestigated. The administration of the main active principle of Cannabis sativa (marijuana), Δ(9)-tetrahydrocannabinol (THC), substantially increases the synthesis of pregnenolone in the brain via activation of the type-1 cannabinoid (CB1) receptor. Pregnenolone then, acting as a signaling-specific inhibitor of the CB1 receptor, reduces several effects of THC. This negative feedback mediated by pregnenolone reveals a previously unknown paracrine/autocrine loop protecting the brain from CB1 receptor overactivation that could open an unforeseen approach for the treatment of cannabis intoxication and addiction.

publication date

  • January 3, 2014

Research

keywords

  • Brain
  • Cannabis
  • Dronabinol
  • Pregnenolone
  • Receptor, Cannabinoid, CB1

Identity

PubMed Central ID

  • PMC4057431

Scopus Document Identifier

  • 84892749496

Digital Object Identifier (DOI)

  • 10.1126/science.1243985

PubMed ID

  • 24385629

Additional Document Info

volume

  • 343

issue

  • 6166