Cannabinoids inhibit GABAergic synaptic transmission in mice nucleus accumbens

Eur J Pharmacol. 2001 Jan 26;412(2):R3-5. doi: 10.1016/s0014-2999(01)00723-3.

Abstract

In mice nucleus accumbens slices, whole-cell patch clamp recording of medium-spiny neurons revealed that cannabimimetics ((R)-(+)-[2,3-dihydro-5-methyl-3-(4-morpholinylmethyl)pyrrolo[1,2,3-de]-1,4-benzoxazin-6-yl]-1-naphtalenylmethanone) (WIN-2) and ((-)-cis-3-[2-hydroxy-4-(1,1-dimethylheptyl)-phenyl]-trans-4-(3-hydroxypropyl)cyclohexanol) inhibit stimulus-evoked gamma-aminobutyric acid mediated inhibitory post-synaptic currents (IPSC). The actions of WIN-2 were reversed by the selective cannabinoid CB(1) receptor antagonist [N-piperidin-1-yl)-5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl-1H-pyrazole-3-carboximide hydrochloride] (SR141716A). WIN-2 modified paired-pulse ratio of evoked IPSCs and decreased miniature IPSC frequency indicating a presynaptic localization of cannabinoid CB(1) receptors.

MeSH terms

  • Analgesics / pharmacology
  • Animals
  • Cannabinoids / pharmacology*
  • Cyclohexanols / pharmacology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Nucleus Accumbens / drug effects*
  • Nucleus Accumbens / physiology
  • Receptors, Cannabinoid
  • Receptors, Drug / drug effects*
  • Receptors, Drug / physiology
  • Synaptic Transmission / drug effects*
  • Synaptic Transmission / physiology
  • gamma-Aminobutyric Acid / drug effects*
  • gamma-Aminobutyric Acid / physiology

Substances

  • Analgesics
  • Cannabinoids
  • Cyclohexanols
  • Receptors, Cannabinoid
  • Receptors, Drug
  • gamma-Aminobutyric Acid
  • 3-(2-hydroxy-4-(1,1-dimethylheptyl)phenyl)-4-(3-hydroxypropyl)cyclohexanol