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Bicuculline-insensitive GABA binding to catfish neuronal membranes
Affiliation:Laboratory of Neurochemistry, Indiana University School of Medicine, 8600 University Boulevard, Evansville, IN 47712, U.S.A.
Abstract:GABA receptor binding to mammalian neuronal membranes has been classified into at least 2 subtypes—GABAA and GABAB binding sites. In catfish brain GABAA receptor sites have previously been demonstrated. Evidence is now presented that under appropriate conditions which rule out GABAA receptor binding, [3H]GABA binds to membranes prepared from catfish brain. This binding is bicuculline-insensitive but differs enough from mammalian GABAB binding to cast some doubt on the idea that GABAB receptors exist in catfish brain. Specific binding was detected that was saturable and exhibited a dissociation constant of 4μM. (±)Baclofen, a potent inhibitor in rat brain, was a weak inhibitor, producing a maximum of 43% inhibition. This inhibitory effect could be enhanced, however, in the presence of 320 μM isoguvacine. [3H]GABA binding was unaffected by bicuculline. Thus bicuculline-insensitive GABA binding sites exist in catfish brain but they differ in a number of ways from the GABAB receptor site found in mammals. Furthermore, a third [3H]GABA binding site appears to exist that is both baclofen- and bicuculline-insensitive, yet is inhibited by high concentrations of isoguvacine, a known GABAA agonist.
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