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dc.contributor.author
Kent, Brianne A.  
dc.contributor.author
Beynon, Amy L.  
dc.contributor.author
Hornsby, Amanda K. E.  
dc.contributor.author
Bekinschtein, Pedro Alejandro  
dc.contributor.author
Bussey, Timothy J.  
dc.contributor.author
Davies, Jeffrey S.  
dc.contributor.author
Saksida, Lisa M.  
dc.date.available
2017-04-26T19:34:23Z  
dc.date.issued
2015-01  
dc.identifier.citation
Kent, Brianne A.; Beynon, Amy L.; Hornsby, Amanda K. E.; Bekinschtein, Pedro Alejandro; Bussey, Timothy J.; et al.; The orexigenic hormone acyl-ghrelin increases adult hippocampal neurogenesis and enhances pattern separation; Pergamon-Elsevier Science Ltd; Psychoneuroendocrinology; 51; 1-2015; 431-439  
dc.identifier.issn
0306-4530  
dc.identifier.uri
http://hdl.handle.net/11336/15761  
dc.description.abstract
An important link exists between intact metabolic processes and normal cognitive functioning; however, the underlying mechanisms remain unknown. There is accumulating evidence that the gut hormone ghrelin, an orexigenic peptide that is elevated during calorie restriction (CR) and known primarily for stimulating growth hormone release, has important extra-hypothalamic functions, such as enhancing synaptic plasticity and hippocampal neurogenesis. The present study was designed to evaluate the long-term effects of elevating acyl-ghrelin levels, albeit within the physiological range, on the number of new adult born neurons in the dentate gyrus (DG) and performance on the Spontaneous Location Recognition (SLR) task, previously shown to be DG-dependent and sensitive to manipulations of plasticity mechanisms and cell proliferation. The results revealed that peripheral treatment of rats with acyl-ghrelin enhanced both adult hippocampal neurogenesis and performance on SLR when measured 8-10 days after the end of acyl-ghrelin treatment. Our data show that systemic administration of physiological levels of acyl-ghrelin can produce long-lasting improvements in spatial memory that persist following the end of treatment. As ghrelin is potentially involved in regulating the relationship between metabolic and cognitive dysfunction in ageing and neurodegenerative disease, elucidating the underlying mechanisms holds promise for identifying novel therapeutic targets and modifiable lifestyle factors that may have beneficial effects on the brain.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Pergamon-Elsevier Science Ltd  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by/2.5/ar/  
dc.subject
ADULT HIPPOCAMPAL NEUROGENESIS  
dc.subject
GHRELIN  
dc.subject
PATTERN SEPARATION  
dc.subject.classification
Otras Ciencias Biológicas  
dc.subject.classification
Ciencias Biológicas  
dc.subject.classification
CIENCIAS NATURALES Y EXACTAS  
dc.title
The orexigenic hormone acyl-ghrelin increases adult hippocampal neurogenesis and enhances pattern separation  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2017-04-26T14:14:22Z  
dc.journal.volume
51  
dc.journal.pagination
431-439  
dc.journal.pais
Países Bajos  
dc.journal.ciudad
Ámsterdam  
dc.description.fil
Fil: Kent, Brianne A.. University of Cambridge; Reino Unido  
dc.description.fil
Fil: Beynon, Amy L.. Swansea University; Reino Unido  
dc.description.fil
Fil: Hornsby, Amanda K. E.. Swansea University; Reino Unido  
dc.description.fil
Fil: Bekinschtein, Pedro Alejandro. University of Cambridge; Reino Unido. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina  
dc.description.fil
Fil: Bussey, Timothy J.. University of Cambridge; Reino Unido  
dc.description.fil
Fil: Davies, Jeffrey S.. Swansea University; Reino Unido  
dc.description.fil
Fil: Saksida, Lisa M.. University of Cambridge; Reino Unido  
dc.journal.title
Psychoneuroendocrinology  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S0306453014003990  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.psyneuen.2014.10.015