4.7 Article

Aripiprazole inhibits marble-burying behavior via 5-hydroxytryptamine (5-HT)1A receptor-independent mechanisms

期刊

EUROPEAN JOURNAL OF PHARMACOLOGY
卷 592, 期 1-3, 页码 103-108

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.ejphar.2008.06.100

关键词

marble-burying behavior; aripiprazole; olanzapine; quetiapine; antipsychotic; 5-HT1A receptor; obsessive-compulsive disorder

资金

  1. Ministry of Education, Culture, Sports, Science and Technology of Japan [18591318]
  2. Eli Lilly and Company (Indianapolis, USA)
  3. AstraZeneca (Wilmington, USA)
  4. Otsuka Pharmaceutical Co., Ltd. (Tokushima, Japan)
  5. Grants-in-Aid for Scientific Research [18591318] Funding Source: KAKEN

向作者/读者索取更多资源

Aripiprazole is a first next-generation atypical antipsychotic drug with dopamine system stabilizing, serotonin (5-hydroxytryptamine, 5-HT) 5-HT1A receptor partial agonistic, and 5-HT2A receptor antagonistic properties. In the present study, we examined the effect of aripiprazole on marble-burying behavior, which has been considered an animal model of obsessive-compulsive disorder, and compared this with the effects of other atypical antipsychotics such as olanzapine and quetiapine. Aripiprazole (1 mg/kg, i.p.) inhibited marble-burying behavior without affecting the locomotor activity in mice. Conversely, olanzapine (3 mg/kg, i.p.) and quetiapine (100 mg/kg, p.o.) showed significant suppression of locomotor activity and impairment of motor coordination at the dose that inhibited marble-burying behavior. On the other hand, a selective 5-HT1A receptor antagonist N-[2-[4-(2-methoxyphenyl)-1-piperazinyl]ethyl]-N-(2-pyridinyl) cyclohexane (WAY100635, 3 mg/kg, i.p.) markedly antagonized the inhibition of marble-burying behavior by 8-hydroxy-2-(di-n-propylamino)tetralin(8-OH-DPAT,3 mg/kg, i.p.),a selective 5-HT1A/7 receptor agonist. By contrast WAY100635 at the same dose had no effect on the inhibition of marble-burying behavior by aripiprazole (1 mg/kg, i.p.). Quinpirole, a dopamine D-2 receptor agonist. showed significant suppression of locomotor activity at the dose that inhibited marble-burying behavior. Conversely, L-741,626, a selective dopamine D2 receptor antagonise at a dose of 10 mg/kg inhibited marble-burying behavior without affecting the locomotor activity. On the other hand, ketanserin, a 5-HT2A receptor antagonist, had no effect on the marble-burying behavior. These findings suggest that aripiprazole may be a useful drug for the treatment of obsessive-compulsive disorder, and that aripiprazole inhibits the marble-burying behavior via 5-HT1A receptor-independent mechanisms. (C) 2008 Elsevier B.V. All rights reserved.

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