Felbamate reduces hormone release and locomotor hypoactivity induced by repeated stress of social defeat in mice
Language English Country Netherlands Media print
Document type Comparative Study, Journal Article, Research Support, Non-U.S. Gov't
PubMed
15695059
DOI
10.1016/j.euroneuro.2004.08.007
PII: S0924-977X(04)00131-2
Knihovny.cz E-resources
- MeSH
- Biogenic Monoamines blood MeSH
- Felbamate MeSH
- Phenylcarbamates MeSH
- Hypokinesia blood drug therapy MeSH
- Corticosterone blood MeSH
- Mice, Inbred ICR MeSH
- Mice MeSH
- Motor Activity drug effects physiology MeSH
- Propylene Glycols pharmacology therapeutic use MeSH
- Stress, Psychological blood drug therapy MeSH
- Social Behavior * MeSH
- Animals MeSH
- Check Tag
- Male MeSH
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Comparative Study MeSH
- Names of Substances
- Biogenic Monoamines MeSH
- Felbamate MeSH
- Phenylcarbamates MeSH
- Corticosterone MeSH
- Propylene Glycols MeSH
Glutamatergic neurotransmission plays a role in stress hormone release and the development of mood diseases. The aim of these studies was to verify the hypothesis that repeated treatment with felbamate, an antiepileptic drug modulating glutamatergic neurotransmission, affects hormone release in response to chronic stress. A mouse model of repeated social defeat (nonaggressive male mouse repeatedly defeated by aggressive counterparts) was used. The results showed that acute treatment with felbamate reduced hypolocomotion in an open field induced by repeated social conflict. The same stress procedure resulted in increased release of corticosterone and dopamine. Felbamate decreased noradrenaline concentrations and inhibited stress-induced rise in corticosterone and dopamine. It is suggested that modulation of stress hormone release may be induced by the action of felbamate on glutamate neurotransmission, and neuroendocrine changes could contribute to behavioural effects of the drug. Antidepressant action of this mood-stabilizing drug suggested by clinicians needs further verification.
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