Effect of synthetic cannabinoids on spontaneous neuronal activity: evaluation using Ca²⁺ spiking and multi-electrode arrays

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DOIResolve DOI: http://doi.org/10.1016/j.ejphar.2016.05.038
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TypeArticle
Journal titleEuropean Journal of Pharmacology
ISSN0014-2999
SubjectCannabinoid receptor 1; neuron; Ca²⁺ spiking; multielectrode array; spice’ compounds
AbstractActivation of cannabinoid receptor 1 (CB₁) inhibits synaptic transmission in hippocampal neurons. The goal of this study was to evaluate the ability of benchmark and emerging synthetic cannabinoids to suppress neuronal activity in vitro using two complementary techniques, Ca²⁺ spiking and multi-electrode arrays (MEAs). Neuron culture and fluorescence imaging conditions were extensively optimized to provide maximum sensitivity for detection of suppression of neural activity by cannabinoids. The neuronal Ca²⁺ spiking frequency was significantly suppressed within 10 min by the prototypic aminoalkylindole cannabinoid, WIN 55,212-2 (10 μM). Suppression by WIN 55,212-2 was not improved by pharmacological intervention with signaling pathways known to interfere with CB₁ signaling. The naphthoylindole CB₁ agonist, JWH-018 suppressed Ca²⁺ spiking at a lower concentration (2.5 μM), and the CB₁ antagonist rimonabant (5 μM), reversed this suppression. In the MEA assay, the ability of synthetic CB₁ agonists to suppress spontaneous electrical activity of hippocampal neurons was evaluated over 80 min sessions. All benchmark (WIN 55,212-2, HU-210, CP 55,940 and JWH-018) and emerging synthetic cannabinoids (XLR-11, JWH-250, 5F-PB-22, AB-PINACA and MAM-2201) suppressed neural activity at a concentration of 10 μM; furthermore, several of these compounds also significantly suppressed activity at 1 μM concentrations. Rimonabant partially reversed spiking suppression of 5F-PB-22 and, to a lesser extent, of MAM-2201, supporting CB₁- mediated involvement, although the inactive WIN 55,212-3 also partially suppressed activity. Taken together, synthetic cannabinoid CB₁-mediated suppression of neuronal activity was detected using Ca²⁺ spiking and MEAs.
Publication date
PublisherElsevier
LanguageEnglish
AffiliationHuman Health Therapeutics; National Research Council Canada
Peer reviewedYes
IdentifierS0014299916303545
NPARC number23000133
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Record identifier77e2df96-2a40-4c35-ae04-a5287af28600
Record created2016-06-07
Record modified2016-06-07
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