Implication of 5-HT2 receptor subtypes in the mechanism of action of the GABAergic compound etifoxine in the four-plate test in Swiss mice
| Autor: | Michel Bourin, Martine Hascoët |
|---|---|
| Rok vydání: | 2010 |
| Předmět: |
Male
Agonist medicine.medical_specialty medicine.drug_class Anxiety Pharmacology Anxiolytic Mice Behavioral Neuroscience chemistry.chemical_compound Internal medicine Oxazines medicine Animals Drug Interactions Analysis of Variance Electroshock Diazepam SB-206553 Behavior Animal Dose-Response Relationship Drug GABAA receptor Chemistry Amphetamines Receptor antagonist Serotonin Receptor Agonists Disease Models Animal Protein Subunits Etifoxine Endocrinology Anti-Anxiety Agents Mechanism of action Receptors Serotonin GABAergic Serotonin Antagonists medicine.symptom Locomotion medicine.drug |
| Zdroj: | Behavioural Brain Research. 208:352-358 |
| ISSN: | 0166-4328 |
| DOI: | 10.1016/j.bbr.2009.11.046 |
| Popis: | Etifoxine is an anxiolytic compound structurally unrelated to benzodiazepine and neurosteroids but potentiating GABA A receptor function by a dual mode of action including a direct positive allosteric modulation through a site distinct from that of benzodiazepines . Etifoxine has been shown to possess some anxiolytic-like effects in rodents. Methods Using the four-plate test (FPT) model of anxiety in mice the potential anxiolytic-like effect of etifoxine was first to re-evaluate. In a second part, in order to better understand the mechanism of action of etifoxine, interaction studies with 5-HT2 ligands were performed in the FPT as mixed serotonergic and GABAergic mechanisms are highly implicated in the anxiolytic-like effect observed in the FPT. Results A dose response effect was observed for etifoxine from the dose of 40–100 mg/kg. Doses above to 60 mg/kg induced a sedative effect as was determined in the actimeter test. The 5-HT2A receptor antagonist SR 46349B blocked the anti-punishment activity of etifoxine (40 and 50 mg/kg), while the 5-HT2B/2C receptor antagonist, SB 206553 and the 5-HT2C receptor antagonist, RS 10-2221 did not alter its effects. In a same way, only the 5-HT2A agonist DOI induced anti-punishment effect when co-administered with subthreshold doses of etifoxine. Conclusion The present results demonstrated that etifoxine effect was modulated by 5-HT2A ligands co-administration. The large literature concerning GABA and 5-HT suggests that they could be co-released and could act as co-transmitters in some regions of the CNS and cross-communication between the two neurotransmitters might be an important modulator process of neuronal activity . |
| Databáze: | OpenAIRE |
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