Cannabinoid signaling in rat cerebellar granule cells: G-protein activation, inhibition of glutamate release and endogenous cannabinoids

• Published in: Neuropharmacology 2004-07, Vol.47 (1), p.81-91
• Main Authors: Breivogel, Christopher S., Walker, J.Michael, Huang, Susan M., Roy, Mary Beth, Childers, Steven R.
• Format: Article
• Language: English
• Subjects: 2-Arachidonoyl glycerol; Anandamide; Animals; Arachidonic Acids - pharmacology; Arachidonyl ethanolamide; Aspartic Acid - secretion; Cannabinoid; Cannabinoids - pharmacology; CB 1 receptor; Cells, Cultured; Cerebellar granule cell; Cerebellum - drug effects; Cerebellum - physiology; Efficacy; Endocannabinoids; Female; G-protein; Glutamic Acid - secretion; GTP-Binding Proteins - drug effects; GTP-Binding Proteins - metabolism; Guanosine 5'-O-(3-Thiotriphosphate) - metabolism; Guanosine-5′- O-(3-thiotriphosphate); Kinetics; Membrane Potentials - drug effects; Membrane Potentials - physiology; Neurons - drug effects; Neurons - physiology; Neurotransmitter release; Polyunsaturated Alkamides; Rats; Rats, Sprague-Dawley; Signal Transduction - drug effects; Signal Transduction - physiology
• ISSN: 0028-3908; 1873-7064
• DOI: 10.1016/j.neuropharm.2004.02.017

Previous studies have indicated that cannabinoids inhibit presynaptic neurotransmitter release in brain through CB 1 receptors. To examine this issue in a primary neuronal culture system, rat cerebellar granule cells (CGCs) were prepared. [ 35S]GTPγS binding assays in saponin-permeabilized CGCs showed that G-protein activation by the CB 1 agonist, WIN55212-2, and adenosine A 1 agonist, phenylisopropyladenosine, was maximal during the second week in culture. △ 9-tetrahydrocannabinol stimulated [ 35S]GTPγS binding to a lesser degree than WIN55212-2, and the antagonists SR141716A and AM281 acted as inverse agonists in intact CGCs, but not in CGC membrane preparations. Ten micromolar WIN55212-2 and △ 9-tetrahydrocannabinol decreased depolarization-evoked efflux of [ 3H]- d-aspartate from CGCs by 32% and 13%, respectively. SR141716A and AM281 increased [ 3H]- d-aspartate release by 28%. The fatty acid amide hydrolase (FAAH) inhibitor phenylmethylsulfonyl fluoride (PMSF) and the anandamide uptake inhibitor AM404 inhibited transmitter release, implying that the antagonist effects were mediated by blockade of endocannabinoid activity. Levels of endocannabinoids (both anandamide and 2-arachidonyl glycerol [2-AG]) in extracts of the cells and cell incubation buffer were increased by PMSF pre-treatment. Depolarization with KCl significantly decreased the amount of anandamide and 2-AG in PMSF-treated CGCs. These results suggest that endogenous cannabinoids inhibit neurotransmitter release in CGCs, which may also release endocannabioids upon neural stimulation.