AM251, a selective antagonist of the CB1 receptor, inhibits the induction of long-term potentiation and induces retrograde amnesia in rats

• Published in: Brain research Vol. 1075; no. 1; pp. 60 - 67
• Main Authors: de Oliveira Alvares, Lucas, Pasqualini Genro, Bruna, Vaz Breda, Ricardo, Pedroso, Michele Franzen, Costa Da Costa, Jaderson, Quillfeldt, Jorge Alberto
• Format: Journal Article
• Language: English
• Published: London Elsevier B.V 23.02.2006; Amsterdam Elsevier; New York, NY
• Subjects: AM251; Amnesia, Retrograde - chemically induced; Amnesia, Retrograde - physiopathology; Animals; Biological and medical sciences; CB1 cannabinoid receptor; Disorders of higher nervous function. Focal brain diseases. Central vestibular syndrome and deafness. Brain stem syndromes; Excitatory Postsynaptic Potentials - drug effects; Excitatory Postsynaptic Potentials - physiology; Hippocampus; Hippocampus - drug effects; Hippocampus - physiology; Hippocampus - physiopathology; Long-Term Potentiation - drug effects; LTP; Male; Medical sciences; Memory; Nervous system (semeiology, syndromes); Neurology; Piperidines - pharmacology; Pyrazoles - pharmacology; Rats; Rats, Wistar; Reaction Time - drug effects; Receptor, Cannabinoid, CB1 - antagonists & inhibitors; CB1 cannabinoid receptor; LTP; AM251; Memory; Hippocampus; Potentiation; Memory disorder; Nervous system diseases; Rat; Rodentia; Central nervous system; Long term; Cerebral disorder; Encephalon; Vertebrata; Mammalia; Animal; Central nervous system disease; Synaptic plasticity; Amnesia; Antagonist; Neurological disorder; Memory LTP AM251 CB1 cannabinoid receptor Hippocampus
• DOI: 10.1016/j.brainres.2005.11.101
• ISSN: 0006-8993

Long-term potentiation (LTP) has a long history as putative mechanism of memory formation, specially in the hippocampus, a structure essential for memory formation. Endocannabinoids are one of the endogenous systems that modulate this plasticity event: the activation of hippocampal CB1 receptors may inhibit local GABA release. Here, we have studied both (1) the role of the selective CB1 antagonist AM251 upon LTP induction in a hippocampal slice preparation, and (2) the effect of its intrahippocampal administration in the step-down inhibitory avoidance (IA) and the open field habituation tasks (OF). Standard extracellular electrophysiology techniques were used to record field excitatory postsynaptic potentials from the dendritic region of CA1 neurons in response to a high frequency stimulation of Schaffer's collaterals; a micropipette ejected 0.2 μM of AM251 (in DMSO/PBS) 2 min before the stimulus: LTP was induced and lasted more than 30 min in the control, but not in the AM251-treated group. Immediately after training, either in IA (footshock, 0.5 mA) or OF, animals received a bilateral infusion of 0.55 or 5.5 ng/side of AM251 or its vehicle in the CA1 region, and test was performed 24 h later. AM251 has caused a significative decrease in the test step-down latency when compared to the control group, but no differences were detected in the OF task, including the number of crossings, i.e., there were no motor effects. The LTP supression could be caused by AM251 acting over GABAergic interneurons that modulate the LTP-bearing glutamatergic neurons. Endocanabinoids would then be the natural dis-inhibitors of local plasticity in the dorsal hippocampus, and the amnestic action of AM251 would be due to a disruption of this endogenous modulatory system.