Molecular and Neuronal Substrate for the Selective Attenuation of Anxiety
pmid: 11021797
Molecular and Neuronal Substrate for the Selective Attenuation of Anxiety
Benzodiazepine tranquilizers are used in the treatment of anxiety disorders. To identify the molecular and neuronal target mediating the anxiolytic action of benzodiazepines, we generated and analyzed two mouse lines in which the α2 or α3 GABA A (γ-aminobutyric acid type A) receptors, respectively, were rendered insensitive to diazepam by a knock-in point mutation. The anxiolytic action of diazepam was absent in mice with the α2(H101R) point mutation but present in mice with the α3(H126R) point mutation. These findings indicate that the anxiolytic effect of benzodiazepine drugs is mediated by α2 GABA A receptors, which are largely expressed in the limbic system, but not by α3 GABA A receptors, which predominate in the reticular activating system.
- University of Zurich Switzerland
- ETH Zurich Switzerland
- Roche (Switzerland) Switzerland
Binding Sites, Diazepam, Patch-Clamp Techniques, Behavior, Animal, Dose-Response Relationship, Drug, Pyramidal Cells, Brain, Receptors, GABA-A, Hippocampus, Synaptic Transmission, Membrane Potentials, Mice, Anti-Anxiety Agents, Phenobarbital, Gene Targeting, Animals, Point Mutation, Female, Cells, Cultured, gamma-Aminobutyric Acid
Binding Sites, Diazepam, Patch-Clamp Techniques, Behavior, Animal, Dose-Response Relationship, Drug, Pyramidal Cells, Brain, Receptors, GABA-A, Hippocampus, Synaptic Transmission, Membrane Potentials, Mice, Anti-Anxiety Agents, Phenobarbital, Gene Targeting, Animals, Point Mutation, Female, Cells, Cultured, gamma-Aminobutyric Acid
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