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Differentiation between low- and high-efficacy CB receptor agonists using a drug discrimination protocol for rats.

Authors :
Järbe, Torbjörn
LeMay, Brian
Halikhedkar, Aneetha
Wood, JodiAnne
Vadivel, Subramanian
Zvonok, Alexander
Makriyannis, Alexandros
Source :
Psychopharmacology. Feb2014, Vol. 231 Issue 3, p489-500. 12p. 1 Diagram, 1 Chart, 8 Graphs.
Publication Year :
2014

Abstract

Rationale: The 'subjective high' from marijuana ingestion is likely due to Δ-tetrahydrocannabinol (THC) activating the central cannabinoid receptor type 1 (CBR) of the endocannabinoid signaling system. THC is a weak partial agonist according to in vitro assays, yet THC mimics the behavioral effects induced by more efficacious cannabinergics. This distinction may be important for understanding similarities and differences in the dose-effect spectra produced by marijuana/THC and designer cannabimimetics ('synthetic marijuana'). Objective: We evaluated if drug discrimination is able to functionally detect/differentiate between a full, high-efficacy CBR agonist [(±)AM5983] and the low-efficacy agonist THC in vivo. Materials and methods: Rats were trained to discriminate between four different doses of AM5983 (0.10 to 0.56 mg/kg), and vehicle and dose generalization curves were determined for both ligands at all four training doses of AM5983. The high-efficacy WIN55,212-2 and the lower-efficacy ( R)-(+)-methanandamide were examined at some AM5983 training conditions. Antagonism tests involved rimonabant and WIN55,212-2 and AM5983. The separate ( S)- and ( R)-isomers of (±)AM5983 were tested at one AM5983 training dose (0.30 mg/kg). The in vitro cyclic adenosine monophosphate (cAMP) assay examined AM5983 and the known CBR agonist CP55,940. Results: Dose generalization ed values increased as a function of the training dose of AM5983, but more so for the partial agonists. The order of potency was ( R)-isomer > (±)AM5983 > ( S)-isomer and AM5983 > WIN55,212-2 ≥ THC > ( R)-(+)-methanandamide. Surmountable antagonism of AM5983 and WIN55,212-2 occurred with rimonabant. The cAMP assay confirmed the cannabinergic nature of AM5983 and CP55,940. Conclusions: Drug discrimination using different training doses of a high-efficacy, full CBR agonist differentiated between low- and high-efficacy CBR agonists. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00333158
Volume :
231
Issue :
3
Database :
Academic Search Index
Journal :
Psychopharmacology
Publication Type :
Academic Journal
Accession number :
93658872
Full Text :
https://doi.org/10.1007/s00213-013-3257-8