No effect of riluzole and memantine on learning deficit following quinpirole sensitization - An animal model of obsessive-compulsive disorder
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
30826389
DOI
10.1016/j.physbeh.2019.01.013
PII: S0031-9384(18)31112-0
Knihovny.cz E-zdroje
- Klíčová slova
- Active allothetic place avoidance task, Memantine, Obsessive-compulsive disorder, Quinpirole, Riluzole,
- MeSH
- agonisté dopaminu farmakologie MeSH
- antagonisté excitačních aminokyselin farmakologie MeSH
- chinpyrol farmakologie MeSH
- chování zvířat účinky léků MeSH
- kognice účinky léků MeSH
- krysa rodu Rattus MeSH
- memantin farmakologie MeSH
- modely nemocí na zvířatech MeSH
- obsedantně kompulzivní porucha * MeSH
- pohybová aktivita účinky léků MeSH
- potkani Long-Evans MeSH
- riluzol farmakologie MeSH
- učení účinky léků MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- agonisté dopaminu MeSH
- antagonisté excitačních aminokyselin MeSH
- chinpyrol MeSH
- memantin MeSH
- riluzol MeSH
RATIONALE: Chronic quinpirole (QNP) sensitization is an established animal model relevant to obsessive-compulsive disorder (OCD) that has been previously shown to induce several OCD-like behavioral patterns, such as compulsive-like checking and increased locomotion. OBJECTIVES: In current study we explored the effect of antiglutamatergic drugs, memantine and riluzole, on cognitive and behavioral performance of QNP sensitized rats. METHODS: During habituation phase, the rats (N = 56) were injected with QNP (0.25 mg/kg) or saline solution (every other day up to 10 injections) and placed into rotating arena without foot shocks for 50-min exploration. Active place avoidance task in rotating arena with unmarked to-be-avoided shock sector was used during acquisition phase. Rats were injected with memantine (1 mg/kg or 5 mg/kg), riluzole (1 mg/kg or 5 mg/kg) or saline solution 30 min before the trial and with QNP (0.25 mg/kg) or saline right before they were placed inside the rotating arena with 60° unmarked shock sector. Locomotion and number of entrances into the shock sector were recorded. RESULTS: QNP sensitization led to a robust deficit in place learning. However, neither memantine nor riluzole did reverse or alleviate the deficit induced by QNP. Contrarily, memantine significantly aggravated QNP induced deficit. CONCLUSIONS: The exacerbation of cognitive deficit following antiglutamatergic agents could be mediated by decreased glutamate concentration in nucleus accumbens and decreased hippocampal activation in the QNP sensitization model.
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