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A Novel Animal Model of Hippocampal Cognitive Deficits, Slow Neurodegeneration, and Neuroregeneration

Long-term adrenalectomy (ADX) results in an extensive and specific loss of dentate gyrus granule cells in the hippocampus of adult rats. This loss of granule cells extends over a period of weeks to months and ultimately results in cognitive deficits revealed in a number of tasks that depend on intac...

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Detalles Bibliográficos
Autores principales: Spanswick, Simon C., Lehmann, Hugo, Sutherland, Robert J.
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3085481/
https://www.ncbi.nlm.nih.gov/pubmed/21541187
http://dx.doi.org/10.1155/2011/527201
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author Spanswick, Simon C.
Lehmann, Hugo
Sutherland, Robert J.
author_facet Spanswick, Simon C.
Lehmann, Hugo
Sutherland, Robert J.
author_sort Spanswick, Simon C.
collection PubMed
description Long-term adrenalectomy (ADX) results in an extensive and specific loss of dentate gyrus granule cells in the hippocampus of adult rats. This loss of granule cells extends over a period of weeks to months and ultimately results in cognitive deficits revealed in a number of tasks that depend on intact hippocampal function. The gradual nature of ADX-induced cell death and the ensuing deficits in cognition resemble in some important respects a variety of pathological conditions in humans. Here, we characterize behavioural and cellular processes, including adult neurogenesis, in the rat ADX model. We also provide experimental evidence for a neurogenic treatment strategy by which the lost hippocampal cells may be replaced, with the goal of functional recovery in mind.
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spelling pubmed-30854812011-05-03 A Novel Animal Model of Hippocampal Cognitive Deficits, Slow Neurodegeneration, and Neuroregeneration Spanswick, Simon C. Lehmann, Hugo Sutherland, Robert J. J Biomed Biotechnol Review Article Long-term adrenalectomy (ADX) results in an extensive and specific loss of dentate gyrus granule cells in the hippocampus of adult rats. This loss of granule cells extends over a period of weeks to months and ultimately results in cognitive deficits revealed in a number of tasks that depend on intact hippocampal function. The gradual nature of ADX-induced cell death and the ensuing deficits in cognition resemble in some important respects a variety of pathological conditions in humans. Here, we characterize behavioural and cellular processes, including adult neurogenesis, in the rat ADX model. We also provide experimental evidence for a neurogenic treatment strategy by which the lost hippocampal cells may be replaced, with the goal of functional recovery in mind. Hindawi Publishing Corporation 2011 2011-03-15 /pmc/articles/PMC3085481/ /pubmed/21541187 http://dx.doi.org/10.1155/2011/527201 Text en Copyright © 2011 Simon C. Spanswick et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Spanswick, Simon C.
Lehmann, Hugo
Sutherland, Robert J.
A Novel Animal Model of Hippocampal Cognitive Deficits, Slow Neurodegeneration, and Neuroregeneration
title A Novel Animal Model of Hippocampal Cognitive Deficits, Slow Neurodegeneration, and Neuroregeneration
title_full A Novel Animal Model of Hippocampal Cognitive Deficits, Slow Neurodegeneration, and Neuroregeneration
title_fullStr A Novel Animal Model of Hippocampal Cognitive Deficits, Slow Neurodegeneration, and Neuroregeneration
title_full_unstemmed A Novel Animal Model of Hippocampal Cognitive Deficits, Slow Neurodegeneration, and Neuroregeneration
title_short A Novel Animal Model of Hippocampal Cognitive Deficits, Slow Neurodegeneration, and Neuroregeneration
title_sort novel animal model of hippocampal cognitive deficits, slow neurodegeneration, and neuroregeneration
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3085481/
https://www.ncbi.nlm.nih.gov/pubmed/21541187
http://dx.doi.org/10.1155/2011/527201
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