Physiological evidence for interaction between the HIV-1 co-receptor CXCR4 and the cannabinoid system in the brain

Br J Pharmacol. 2009 Aug;157(7):1225-31. doi: 10.1111/j.1476-5381.2009.00285.x. Epub 2009 Jun 22.

Abstract

Background and purpose: The chemokine, stromal cell-derived growth factor-1alpha (SDF-1alpha/CXCL12), a member of the CXC chemokine family, and the ligand for CXCR4, the co-receptor involved in the entry of human immunodeficiency virus-1 (HIV-1), was tested for its possible interaction with a physiological response to a cannabinoid.

Experimental approach: The cannabinoid agonist, an aminoalkylindole, (+)-WIN 55,212-2 [(4,5-dihydro-2-methyl-4(4-morpholinylmethyl)-1-(1-naphthalenyl-carbonyl)-6H-pyrrolo[3,2,1ij]quinolin-6-one], was infused directly into the preoptic anterior hypothalamus (POAH), the primary brain area involved in thermoregulation.

Key results: WIN 55,212-2 (5-15 microg) evoked a dose-related hypothermia, which was attenuated by SDF-1alpha/CXCL12 microinjected directly into the POAH. The inhibitory effect of SDF-1alpha/CXCL12 on WIN 55,212-2-induced hypothermia was reversed by 1,1'-[1,4-phenylenebis(methylene)]bis[1,4,8,11-tetraazacyclotetradecane] octohydrobromide dihydrate, an antagonist of SDF-1alpha/CXCL12, acting at its receptor, CXCR4.

Conclusion and implications: This study provides the first in vivo evidence for a thermoregulatory interaction between the HIV-1 co-receptor and the cannabinoid system in the brain.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Benzoxazines / pharmacology
  • Body Temperature / drug effects
  • Cannabinoids / agonists
  • Cannabinoids / metabolism*
  • Chemokine CXCL12 / physiology*
  • HIV-1 / physiology*
  • Male
  • Microinjections
  • Morpholines / pharmacology
  • Naphthalenes / pharmacology
  • Preoptic Area / drug effects
  • Preoptic Area / metabolism*
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, CXCR4 / physiology*

Substances

  • Benzoxazines
  • Cannabinoids
  • Chemokine CXCL12
  • Cxcr4 protein, rat
  • Morpholines
  • Naphthalenes
  • Receptors, CXCR4
  • (3R)-((2,3-dihydro-5-methyl-3-((4-morpholinyl)methyl)pyrrolo-(1,2,3-de)-1,4-benzoxazin-6-yl)(1-naphthalenyl))methanone