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dc.creatorPitsikas, N.en
dc.date.accessioned2015-11-23T10:45:41Z
dc.date.available2015-11-23T10:45:41Z
dc.date.issued2009
dc.identifier10.1016/j.bbr.2009.01.014
dc.identifier.issn0166-4328
dc.identifier.urihttp://hdl.handle.net/11615/32295
dc.description.abstractNitric oxide (NO) is considered as an intracellular messenger in the brain. Its involvement in learning and memory processes has been proposed. Compounds that inhibit NO synthase (NOS), the key synthesizing enzyme, may inhibit cognition, while NO donors may facilitate it. The present study was designed to investigate the effects of the NO donor molsidomine on rats' spatial memory. Thus, the ability of molsidomine (2 and 4 mg/kg, i.p.) in attenuating spatial memory deficits produced either by the muscarinic receptor antagonist scopolamine (0.2 mg/kg, s.c.) or by the NOS inhibitor L-NAME (30 mg/kg, i.p.) was assessed. For this aim, the object location test was selected. In the first study, molsidomine (4 mg/kg) counteracted the scopolamine-induced performance deficits in this spatial memory task. Subsequently, pre-training administration of molsidomine (4 mg/kg but not 2 mg/kg) antagonized also the impairing effects produced by L-NAME in the object location paradigm. These results indicate that NO is involved in spatial recognition memory and that an NO component modulates the effects of the cholinergic system on spatial memory. (C) 2009 Elsevier B.V. All rights reserved.en
dc.sourceBehavioural Brain Researchen
dc.source.uri<Go to ISI>://WOS:000265510300023
dc.subjectObject locationen
dc.subjectSpatial memoryen
dc.subjectScopolamineen
dc.subjectNitric oxideen
dc.subjectL-NAMEen
dc.subjectMolsidomineen
dc.subjectRaten
dc.subject14-UNIT T-MAZEen
dc.subjectOBJECT RECOGNITIONen
dc.subjectLOCATION MEMORYen
dc.subjectL-ARGININEen
dc.subjectHIPPOCAMPUSen
dc.subjectIMPAIRMENTen
dc.subjectGLUTAMATEen
dc.subjectRELEASEen
dc.subjectSYSTEMen
dc.subjectBehavioral Sciencesen
dc.subjectNeurosciencesen
dc.titleThe nitric oxide (NO) donor molsidomine antagonizes scopolamine and L-NAME-induced performance deficits in a spatial memory task in the raten
dc.typejournalArticleen


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