Εμφάνιση απλής εγγραφής

dc.creatorPitsikas, N.en
dc.creatorSakellaridis, N.en
dc.date.accessioned2015-11-23T10:45:43Z
dc.date.available2015-11-23T10:45:43Z
dc.date.issued2007
dc.identifier10.1016/j.ejphar.2007.06.019
dc.identifier.issn0014-2999
dc.identifier.urihttp://hdl.handle.net/11615/32312
dc.description.abstractThe effects of the non-competitive N-methyl-D-aspartate (NMDA) receptor antagonist memantine on recognition memory were investigated in the rat by using the object recognition task. In addition, a possible interaction between memantine and the nitric oxide (NO) donor molsidomine in antagonizing extinction of recognition memory was also evaluated utilizing the same behavioral procedure. In a first dose-response study, post-training administration of memantine (10 and 20, but not 3 mg/kg) antagonized recognition memory deficits in the rat, suggesting that memantine modulates storage and/or retrieval of information. In a subsequent study, combination of sub-threshold doses of memantine (3 mg/kg) and the NO donor molsidomine (1 mg/kg) counteracted delay-dependent impairments in the same task. Neither memantine (3 mg/kg) nor molsidomine (1 mg/kg) alone reduced object recognition performance deficits. The present findings indicate a) that memantine is involved in recognition memory and b) support a functional interaction between memantine and molsidomine on recognition memory mechanisms. (C) 2007 Elsevier B.V. All rights reserved.en
dc.sourceEuropean Journal of Pharmacologyen
dc.source.uri<Go to ISI>://WOS:000250043400013
dc.subjectNMDAen
dc.subjectnitric oxideen
dc.subjectmemantineen
dc.subjectmolsidomineen
dc.subjectrecognition memoryen
dc.subject(rat)en
dc.subjectNMDA RECEPTOR ANTAGONISTen
dc.subjectLONG-TERM POTENTIATIONen
dc.subjectFREELY MOVING RATSen
dc.subjectMETHYL-D-ASPARTATEen
dc.subjectOBJECT-RECOGNITIONen
dc.subjectALZHEIMERS-DISEASEen
dc.subjectL-NAMEen
dc.subjectGLUTAMATEen
dc.subjectHIPPOCAMPUSen
dc.subjectMODULATIONen
dc.subjectPharmacology & Pharmacyen
dc.titleMemantine and recognition memory: Possible facilitation of its behavioral effects by the nitric oxide (NO) donor molsidomineen
dc.typejournalArticleen


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