Morris water maze learning in Long-Evans rats is differentially affected by blockade of D1-like and D2-like dopamine receptors
Jazyk angličtina Země Irsko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
17611026
DOI
10.1016/j.neulet.2007.06.012
PII: S0304-3940(07)00699-4
Knihovny.cz E-zdroje
- MeSH
- antagonisté dopaminu D2 * MeSH
- antagonisté dopaminu farmakologie MeSH
- bludiště - učení účinky léků fyziologie MeSH
- chování zvířat účinky léků MeSH
- krysa rodu Rattus MeSH
- potkani inbrední LEC MeSH
- receptory dopaminu D1 antagonisté a inhibitory 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
- antagonisté dopaminu D2 * MeSH
- antagonisté dopaminu MeSH
- receptory dopaminu D1 MeSH
Dopaminergic neurotransmission is involved in several brain functions including spatial cognition. In the present study we examine the effects of systemic administration of D1-like receptor antagonist SCH23390 and D2-like receptor antagonist sulpiride on the acquisition of the Morris water maze task. We used visible versus hidden platform versions of the MWM in order to distinguish between the effects of the drugs on the procedural versus cognitive aspects of the task. SCH23390 was found to prolong escape latencies to the visible platform at a higher dose (0.05mg/kg), whilst the lower dose (0.02mg/kg) left both procedural and cognitive functions almost unchanged. SCH23390 was also found to reduce swimming speed. Sulpiride did not affect the visible platform learning at any of three doses studied (30, 60 and 100mg/kg); the highest dose of sulpiride (100mg/kg) impaired place navigation to the hidden platform, without affecting the swim speed. The results of the present study show a difference in the involvement of D1-like and D2-like receptors in the MWM acquisition.
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