Morris water maze learning in Long-Evans rats is differentially affected by blockade of D1-like and D2-like dopamine receptors
Language English Country Ireland Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
17611026
DOI
10.1016/j.neulet.2007.06.012
PII: S0304-3940(07)00699-4
Knihovny.cz E-resources
- MeSH
- Dopamine D2 Receptor Antagonists * MeSH
- Dopamine Antagonists pharmacology MeSH
- Maze Learning drug effects physiology MeSH
- Behavior, Animal drug effects MeSH
- Rats MeSH
- Rats, Inbred LEC MeSH
- Receptors, Dopamine D1 antagonists & inhibitors MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Male MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Dopamine D2 Receptor Antagonists * MeSH
- Dopamine Antagonists MeSH
- Receptors, Dopamine 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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