The involvement of the polyamines binding sites at the NMDA receptor in creatine-induced spatial learning enhancement

Achievements made over the last years have highlighted the important role of creatine in health and disease. However, studies of its effect on cognition function have been limited. In the present study, we investigated the effect of creatine on early consolidation of the spatial learning in rats. St...

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Published inBehavioural brain research Vol. 187; no. 1; pp. 200 - 204
Main Authors Oliveira, Mauro Schneider, Furian, Ana Flávia, Fighera, Michele Rechia, Fiorenza, Natália Gindri, Ferreira, Juliano, Rubin, Maribel Antonello, Mello, Carlos Fernando, Royes, Luiz Fernando Freire
Format Journal Article
LanguageEnglish
Published Shannon Elsevier B.V 11.02.2008
Elsevier Science
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Summary:Achievements made over the last years have highlighted the important role of creatine in health and disease. However, studies of its effect on cognition function have been limited. In the present study, we investigated the effect of creatine on early consolidation of the spatial learning in rats. Statistical analysis showed that intrahippocampal administration of creatine (2.5 and 7.5 nmol/hippocampus) (post-training) decreased the latency for scape and mean number of errors in Barnes maze test. The involvement of polyamine binding site at NMDA receptor in creatine-induced spatial learning enhancement was investigated by co-administration of arcaine (0.02 nmol/hippocampus) or spermidine (0.02 nmol/hippocampus) with creatine (2.5 nmol/hippocampus) (post-training). Statistical analysis revealed that creatine-induced spatial learning enhancement was reverted by co-administration of arcaine (0.02 nmol/hippocampus) and intensified by spermidine (0.02 nmol/hippocampus). These results provide evidence that creatine not only seem to be involved in energy metabolism but may also play an important role in early consolidation of spatial learning in hippocampus which participation of polyamines binding site at the NMDA receptor.
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ISSN:0166-4328
1872-7549
DOI:10.1016/j.bbr.2007.09.004