부산대학교 도서관

Rationale GABA.sub.A [alpha]5 subunit-containing receptors are primarily expressed in the hippocampus and their role in learning and memory has been demonstrated recently by both genetic and pharmacological approaches. Objectives The objective of the study is to evaluate the cognitive effects of a novel GABA.sub.A [alpha]5 receptor inverse agonist, RO4938581 in rats and monkeys. Materials and methods The in vitro profile was determined using radioligand binding and electrophysiological assays for the GABA.sub.A [alpha]1, [alpha]2, [alpha]3, and [alpha]5 receptors. Long-term potentiation (LTP) was performed in mouse hippocampal slices. Cognitive effects were assessed in rats in the delayed match to position (DMTP) task and the Morris water maze. In monkeys, the object retrieval task was used. Pro-convulsant and anxiogenic potentials were evaluated in mice and rats. In vivo receptor occupancy was determined using [[.sup.3]H]-RO0154513. Results RO4938581 is a potent inverse agonist at the GABA.sub.A [alpha]5 receptor, with both binding and functional selectivity, enhancing hippocampal LTP. RO4938581 reversed scopolamine-induced working memory impairment in the DMTP task (0.3--1 mg/kg p.o.) and diazepam-induced spatial learning impairment (1--10 mg/kg p.o.). RO4938581 improved executive function in monkeys (3-10 mg/kg p.o.). Importantly, RO4938581 showed no anxiogenic and pro-convulsive potential. RO4938581 dose-dependently bound to GABA.sub.A [alpha]5 receptors and approximately 30% receptor occupancy was sufficient to produce enhanced cognition in the rat. Conclusions The data further support the potential of GABA.sub.A [alpha]5 receptors as a target for cognition-enhancing drugs. The dual binding and functional selectivity offers an ideal profile for cognition-enhancing effects without the unwanted side effects associated with activity at other GABA.sub.A receptor subtypes.