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Regional preferences of AMPA receptor modulators determined through agonist binding autoradiography
Authors:Markus Kessler  Manpreet S Mutneja  Gary Rogers  Gary Lynch
Affiliation:aCenter for the Neurobiology of Learning and Memory, University of California, Irvine, CA 92697-3800, USA;bCortex Pharmaceuticals, Irvine, CA 92618, USA
Abstract:Autoradiographic techniques were used to test if positive modulators of AMPA-type glutamate receptors have regionally differentiated effects on ligand binding. Cyclothiazide, a drug with ten fold greater effects on `flip' than `flop' splice variants of the receptors, had unequal effects across the subdivisions of hippocampus; i.e., it reduced [3H]AMPA binding in field CA3 with an EC50 of 24 μM and in field CA1 and dentate gyrus with EC50s between 60 and 100 μM. The EC50 for the drug's influence on binding was also significantly lower in the superficial than in the deeper layers of the neocortex, though these differences were not as pronounced as those in the hippocampus. The ampakine CX614, a compound with a modest preference for flop variants, had a slightly lower EC50 for its effects on [3H]AMPA binding in CA1 than in CA3. This result was confirmed with [3H]fluorowillardiine binding. The effects of the ampakine in neocortex tended to be greater in the deeper than superficial layers but this did not reach statistical significance. These results indicate that differential effects of modulators on AMPA receptor subunits are reflected in their relative potency across brain subdivisions. This raises the possibility that subclasses of positive modulators will exhibit a measurable degree of selectivity in their physiological and behavioral influences.
Keywords:CX614   Ampakine   Cyclothiazide   Fluorowillardiine   Hippocampus   Cortex
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