Abstract
The effect of the benzodiazepine receptor antagonist flumazenil was examined on an antiaggressive effect of (S)-5-[3-[(1,4-benzodioxan-2-ylmethyl)amino]propoxy]-1,3- benzodioxole HCl (MKC-242), a 5-HT(1A) receptor agonist. MKC-242 (0.1-1.0 mg/kg, p.o.) selectively reduced isolation-induced aggressive behavior in a dose-dependent manner. Flumazenil (10 mg/kg, i.p.) antagonized the antiaggressive effects of MKC-242 and diazepam, although it alone did not affect the behaviors of isolated mice. These findings suggest that a gamma-aminobutyric acid(A) (GABA(A)) receptor system is involved in the antiaggressive effect by 5-HT(1A) receptor activation.
Publication types
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Aggression / drug effects*
-
Animals
-
Behavior, Animal / drug effects
-
Binding Sites
-
Diazepam / pharmacology
-
Dioxanes / pharmacology*
-
Dioxoles / pharmacology*
-
Dose-Response Relationship, Drug
-
Flumazenil / pharmacology
-
GABA Modulators / pharmacology
-
Male
-
Mice
-
Piperazines / pharmacology
-
Pyridines / pharmacology
-
Receptors, GABA-A / drug effects
-
Receptors, GABA-A / metabolism*
-
Receptors, Serotonin / drug effects*
-
Receptors, Serotonin / metabolism
-
Receptors, Serotonin, 5-HT1
-
Serotonin Antagonists / pharmacology
-
Serotonin Receptor Agonists / pharmacology*
-
Social Isolation
Substances
-
Dioxanes
-
Dioxoles
-
GABA Modulators
-
Piperazines
-
Pyridines
-
Receptors, GABA-A
-
Receptors, Serotonin
-
Receptors, Serotonin, 5-HT1
-
Serotonin Antagonists
-
Serotonin Receptor Agonists
-
Flumazenil
-
N-(2-(4-(2-methoxyphenyl)-1-piperazinyl)ethyl)-N-(2-pyridinyl)cyclohexanecarboxamide
-
osemozotan
-
Diazepam