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   <subfield code="a">Two Mouse Lines Selected for Differential Sensitivities to β-Carboline-Induced Seizures Are Also differentially Sensitive to Various Pharmacological Effects of Other GABAA Receptor Ligands</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Daisy Rinaldi, Benjamin Boutre, Joelle Adrien, Patrice Venault, Georges Chapouthier]</subfield>
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   <subfield code="a">Two mouse lines were selectively bred according to their sensitivity (BS line) or resistance (BR line) to seizures induced by a single i.p. injection of methyl β-carboline-3-carboxylate (β-CCM), an inverse agonist of the GABAA receptor benzodiazepine site. Our aim was to characterize both lines' sensitivities to various physiological effects of other ligands of the GABAA receptor. We measured diazepam-induced anxiolysis with the elevated plus-maze test, diazepam-induced sedation by recording the vigilance states, and picrotoxin- and pentylenetetrazol-induced seizures after i.p. injections. Results presented here show that the differential sensitivities of BS and BR lines to β-CCM can be extended to diazepam, picrotoxin, and pentylenetetrazol, suggesting a genetic selection of a general sensitivity and resistance to several ligands of the GABAA receptor.</subfield>
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