WIN55,212-2 induced deficits in spatial learning are mediated by cholinergic hypofunction

Cannabinoids acting on CB 1 receptors induce learning and memory impairments. However, the identification of novel non-CB 1 receptors which are insensitive to the psychoactive ingredient of marijuana, Δ 9-tetrahydrocannabinol (Δ 9-THC) but sensitive to synthetic cannabinoids such as WIN55,212-2 (WIN...

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Published in:	Behavioural brain research 2010-04, Vol.208 (2), p.584-592
Main Authors:	Robinson, Lianne, Goonawardena, Anushka V., Pertwee, Roger, Hampson, Robert E., Platt, Bettina, Riedel, Gernot
Format:	Article
Language:	eng
Subjects:	Acetylcholine - metabolism Animals Behavioral psychophysiology Benzoxazines - pharmacology Biological and medical sciences Cannabinoid Cannabinoid Receptor Agonists Cholinergic Antagonists - pharmacology Cholinesterase inhibitor Disease Models, Animal Dizocilpine Maleate - pharmacology Dose-Response Relationship, Drug Drug Interactions Excitatory Amino Acid Antagonists - pharmacology Fundamental and applied biological sciences. Psychology Learning Disabilities - chemically induced Learning Disabilities - metabolism Male Maze Learning - drug effects Medical sciences Memory - drug effects Morpholines - pharmacology Naphthalenes - pharmacology Neuropharmacology Pharmacology. Drug treatments Piperidines - pharmacology Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer..., (alzheimer disease) Psychology. Psychoanalysis. Psychiatry Psychology. Psychophysiology Psychopharmacology Pyrazoles - pharmacology Rat Rats Rimonabant Rivastigmine Scopolamine - pharmacology Spatial Behavior - drug effects Spatial learning Water maze WIN-55,212-2
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Summary:	Cannabinoids acting on CB 1 receptors induce learning and memory impairments. However, the identification of novel non-CB 1 receptors which are insensitive to the psychoactive ingredient of marijuana, Δ 9-tetrahydrocannabinol (Δ 9-THC) but sensitive to synthetic cannabinoids such as WIN55,212-2 (WIN-2) or endocannabinoids like anandamide lead us to question whether WIN-2 induced learning and memory deficits are indeed mediated by CB 1 receptor activation. Given the relative paucity of receptor subtype specific antagonists, a way forward would be to determine the transmitter systems, which are modulated by the respective cannabinoids. This study set out to evaluate this proposition by determination of the effects of WIN-2 on acquisition of spatial reference memory using the water maze in rats. Particular weight was given to performance in trial 1 of each daily session as an index of between-session long-term memory, and in trial 4 as an index of within-session short-term memory. Intraperitoneal (i.p.) administration of WIN-2 (1 mg/kg and 3 mg/kg) prior to training impaired long-term, but not short-term memory. This deficit was not reversed by the CB 1 antagonists/inverse agonists Rimonabant (3 mg/kg i.p.) and AM281 (0.5 mg/kg i.p.), but recovered in the presence of the cholinesterase inhibitor rivastigmine (1 mg/kg). Reversal by rivastigmine was specific to WIN-2, as it failed to reverse MK801 (0.08 mg/kg) induced learning impairments. Collectively, these data suggest that in this spatial reference memory task WIN-2 causes a reduction in cholinergic activation, possibly through a non-CB 1-like mechanism, which affects long-term but not short-term spatial memory.
ISSN:	0166-4328 1872-7549