Dexmedetomidine selectively suppresses dominant behaviour in aggressive and sociable mice
Language English Country Netherlands Media print-electronic
Document type Comparative Study, Journal Article, Research Support, Non-U.S. Gov't
PubMed
16226250
DOI
10.1016/j.ejphar.2005.08.022
PII: S0014-2999(05)00842-3
Knihovny.cz E-resources
- MeSH
- Adrenergic alpha-Agonists administration & dosage pharmacology MeSH
- Aggression drug effects MeSH
- Adrenergic alpha-Antagonists administration & dosage pharmacology MeSH
- Receptors, Adrenergic, alpha-2 drug effects MeSH
- Analysis of Variance MeSH
- Behavior, Animal drug effects MeSH
- Dexmedetomidine administration & dosage pharmacology MeSH
- Imidazoles administration & dosage pharmacology MeSH
- Conflict, Psychological MeSH
- Mice, Inbred ICR MeSH
- Mice MeSH
- Motor Activity drug effects MeSH
- Social Behavior * MeSH
- Dose-Response Relationship, Drug 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
- Adrenergic alpha-Agonists MeSH
- Adrenergic alpha-Antagonists MeSH
- Receptors, Adrenergic, alpha-2 MeSH
- atipamezole MeSH Browser
- Dexmedetomidine MeSH
- Imidazoles MeSH
Dexmedetomidine is a highly specific alpha2-adrenoreceptor agonist, which is now clinically used to induce sedation in patients in the intensive care units. Behavioural effects of dexmedetomidine have been little studied so far. The drug was reported to reduce behaviour such as locomotion or measures of anxiety or aggression in animals. The aim of the present study was to ascertain whether dexmedetomidine inhibits behaviour uniformly or with respect to particular stimuli or situations. Therefore, behavioural effects of dexmedetomidine were studied in the social conflict test in male mice (after three weeks of individual housing), which provides a wide spectrum of behavioural activities in two types of animals (aggressive and sociable mice) as well as in the activity cage. Dexmedetomidine (5-40 microg/kg i.p.) decreased locomotion in the activity cage and this effect was fully antagonized by atipamezole, a selective alpha2-adrenereceptor antagonist. However, dexmedetomidine did not reduce locomotion during social conflict. The only significant effects during social conflict were a selective and dose-dependent antiaggressive effect in aggressive mice and a selective reduction of social investigation ('sociability') in sociable mice. Thus, dexmedetomidine appears to inhibit predominantly dominant behaviour evoked by biologically important stimuli. The ability of dexmedetomidine to reduce aggression might be utilized for treatment of aggressive states. Sedation caused by dexmedetomidine can be easily disrupted and thus the drug may have an advantage over benzodiazepines or neuroleptics, which are used in this indication.
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