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[INCREMENT]9-Tetrahydrocannabinol discriminative stimulus effects of AM2201 and related aminoalkylindole analogs in rats.


ABSTRACT: The recent recreational use of synthetic cannabinoid ligands, collectively referred to as 'Spice', has raised concerns about their safety and possible differences in their biological effect(s) from marijuana/?-tetrahydrocannabinol (THC). AM2201, a highly efficacious, potent cannabinoid receptor 1 (CB1R) agonist, is a recently detected compound in 'Spice' preparations. Furthermore, structural analogs of AM2201 are now being found in 'Spice'. The present studies were conducted to investigate their ?-THC-like effects using drug (?-THC) discrimination in rats. Results show that the tested compounds were potent cannabinergics that generalized to the response to ?-THC, with AM2201 being most potent, exhibiting a 14-fold potency difference over ?-THC. The other analogs were between 2.5-fold and 4-fold more potent than THC. Surmountable antagonism of AM2201 with the selective CB1R antagonist/inverse agonist rimonabant also established that the discrimination is CB1R dependent. Time-course data reveal that AM2201 likely peaks rapidly with an in-vivo functional half-life of only 60?min. The present data confirm and extend previous observations regarding ?-THC-like effects of 'Spice' components.

SUBMITTER: Jarbe TU 

PROVIDER: S-EPMC4779682 | biostudies-literature | 2016 Apr

REPOSITORIES: biostudies-literature

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[INCREMENT]9-Tetrahydrocannabinol discriminative stimulus effects of AM2201 and related aminoalkylindole analogs in rats.

Järbe Torbjörn U C TU   Gifford Roger S RS   Zvonok Alexander A   Makriyannis Alexandros A  

Behavioural pharmacology 20160401 2-3 Spec Issue


The recent recreational use of synthetic cannabinoid ligands, collectively referred to as 'Spice', has raised concerns about their safety and possible differences in their biological effect(s) from marijuana/Δ-tetrahydrocannabinol (THC). AM2201, a highly efficacious, potent cannabinoid receptor 1 (CB1R) agonist, is a recently detected compound in 'Spice' preparations. Furthermore, structural analogs of AM2201 are now being found in 'Spice'. The present studies were conducted to investigate their  ...[more]

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