Anxiogenic effects of the intraamygdala injection of flumazenil, a benzodiazepine receptor antagonist.
Cláudio Da Cunha, C. Wolfman, M. Levi de Stein, Anelise C. Ruschel, Iñaki Izquierdo, Jorge Horacio Medina
Abstract
Cláudio Da Cunha, C. Wolfman, M. Levi de Stein, Anelise C. Ruschel, Iñaki Izquierdo, Jorge Horacio Medina
Abstract
The effects of bilateral intraamygdala microinjection of flumazenil, a benzodiazepine receptor (BZD-R) antagonist, on the exploratory activity in an elevated plus maze were examined in chronically implanted rats. This compound induced a significant decrease in the time spent in the open arms, which is consistent with an anxiogenic action. No effect was observed after intrastriatal injections of flumazenil. Naive rats exposed to the elevated plus maze showed a rapid and selective decline in the content of BZD-like molecules in amygdala (-68%) but not in striatum and hippocampus. These data suggest that the anxiogenic effects of the intraamygdala injection of flumazenil is probably due to the blockade of BZD-like molecules released during the performance.
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The effects of bilateral intraamygdala microinjection of flumazenil, a benzodiazepine receptor (BZD-R) antagonist, on the exploratory activity in an elevated plus maze were examined in chronically implanted rats. This compound induced a significant decrease in the time spent in the open arms, which is consistent with an anxiogenic action. No effect was observed after intrastriatal injections of flumazenil. Naive rats exposed to the elevated plus maze showed a rapid and selective decline in the content of BZD-like molecules in amygdala (-68%) but not in striatum and hippocampus. These data suggest that the anxiogenic effects of the intraamygdala injection of flumazenil is probably due to the blockade of BZD-like molecules released during the performance.
Key concepts: Flumazenil, Anxiogenic, Benzodiazepine, Antagonist, Microinjection, Elevated plus maze, Pharmacology, Endocrinology