Oxiracetam prevented the scopolamine but not the diazepam induced memory deficits in mice
Jazyk angličtina Země Nizozemsko Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
12110475
DOI
10.1016/s0166-4328(02)00028-1
PII: S0166432802000281
Knihovny.cz E-zdroje
- MeSH
- antagonisté muskarinových receptorů farmakologie MeSH
- bludiště - učení účinky léků MeSH
- diazepam farmakologie MeSH
- GABA modulátory farmakologie MeSH
- myši MeSH
- nootropní látky farmakologie MeSH
- poruchy paměti chemicky indukované prevence a kontrola MeSH
- přenos učení (psychologie) účinky léků MeSH
- pyrrolidiny farmakologie MeSH
- skopolamin antagonisté a inhibitory farmakologie MeSH
- úzkost psychologie MeSH
- zvířata MeSH
- Check Tag
- myši MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- antagonisté muskarinových receptorů MeSH
- diazepam MeSH
- GABA modulátory MeSH
- nootropní látky MeSH
- oxiracetam MeSH Prohlížeč
- pyrrolidiny MeSH
- skopolamin MeSH
In mice, the elevated plus-maze paradigm was used to investigate the effect of scopolamine hydrobromide and diazepam and their interaction with oxiracetam on the retrieval of spatial memory trace. This paradigm measures (using the transfer latency) an animal's capacity to escape from the open arm to the enclosed one. The retention session followed 24 h after the acquisition one. Experiment 1: Scopolamine (0.25 and 0.5 mg/kg) and diazepam (0.5 and 1.0 mg/kg) given 30 min before the retention session significantly prolonged the transfer latency as compared with the saline treated mice and those given the lowest dose of scopolamine (0.125 mg/kg) and diazepam (0.25 mg/kg). Experiment 2: Oxiracetam administered at doses of 3, 10 and 30 mg/kg immediately after the acquisition session prevented the scopolamine induced prolongation of the transfer latency. Thus, oxiracetam forestalled the impairment of retrieval of memory trace: the animals were able to remember the spatial configuration of the plus-maze. On the contrary, oxiracetam was not effective in the diazepam treated mice. We suggest that beneficial effect of oxiracetam might be confounded or blocked by the anxiolytic effect of diazepam.
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