Cargando…

Brain tissue oxygen amperometry in behaving rats demonstrates functional dissociation of dorsal and ventral hippocampus during spatial processing and anxiety

Traditionally, the function of the hippocampus (HPC) has been viewed in unitary terms, but there is growing evidence that the HPC is functionally differentiated along its septotemporal axis. Lesion studies in rodents and functional brain imaging in humans suggest a preferential role for the septal H...

Descripción completa

Detalles Bibliográficos
Autores principales: McHugh, Stephen B, Fillenz, Marianne, Lowry, John P, Rawlins, J Nicolas P, Bannerman, David M
Formato: Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3085075/
https://www.ncbi.nlm.nih.gov/pubmed/21105915
http://dx.doi.org/10.1111/j.1460-9568.2010.07497.x
_version_ 1782202591046795264
author McHugh, Stephen B
Fillenz, Marianne
Lowry, John P
Rawlins, J Nicolas P
Bannerman, David M
author_facet McHugh, Stephen B
Fillenz, Marianne
Lowry, John P
Rawlins, J Nicolas P
Bannerman, David M
author_sort McHugh, Stephen B
collection PubMed
description Traditionally, the function of the hippocampus (HPC) has been viewed in unitary terms, but there is growing evidence that the HPC is functionally differentiated along its septotemporal axis. Lesion studies in rodents and functional brain imaging in humans suggest a preferential role for the septal HPC in spatial learning and a preferential role for the temporal HPC in anxiety. To better enable cross-species comparison, we present an in vivo amperometric technique that measures changes in brain tissue oxygen at high temporal resolution in freely-moving rats. We recorded simultaneously from the dorsal (septal; dHPC) and ventral (temporal; vHPC) HPC during two anxiety tasks and two spatial tasks on the radial maze. We found a double-dissociation of function in the HPC, with increased vHPC signals during anxiety and increased dHPC signals during spatial processing. In addition, dHPC signals were modulated by spatial memory demands. These results add a new dimension to the growing consensus for a differentiation of HPC function, and highlight tissue oxygen amperometry as a valuable tool to aid translation between animal and human research.
format Text
id pubmed-3085075
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher Blackwell Publishing Ltd
record_format MEDLINE/PubMed
spelling pubmed-30850752011-05-13 Brain tissue oxygen amperometry in behaving rats demonstrates functional dissociation of dorsal and ventral hippocampus during spatial processing and anxiety McHugh, Stephen B Fillenz, Marianne Lowry, John P Rawlins, J Nicolas P Bannerman, David M Eur J Neurosci Behavioral Neuroscience Traditionally, the function of the hippocampus (HPC) has been viewed in unitary terms, but there is growing evidence that the HPC is functionally differentiated along its septotemporal axis. Lesion studies in rodents and functional brain imaging in humans suggest a preferential role for the septal HPC in spatial learning and a preferential role for the temporal HPC in anxiety. To better enable cross-species comparison, we present an in vivo amperometric technique that measures changes in brain tissue oxygen at high temporal resolution in freely-moving rats. We recorded simultaneously from the dorsal (septal; dHPC) and ventral (temporal; vHPC) HPC during two anxiety tasks and two spatial tasks on the radial maze. We found a double-dissociation of function in the HPC, with increased vHPC signals during anxiety and increased dHPC signals during spatial processing. In addition, dHPC signals were modulated by spatial memory demands. These results add a new dimension to the growing consensus for a differentiation of HPC function, and highlight tissue oxygen amperometry as a valuable tool to aid translation between animal and human research. Blackwell Publishing Ltd 2011-01 /pmc/articles/PMC3085075/ /pubmed/21105915 http://dx.doi.org/10.1111/j.1460-9568.2010.07497.x Text en European Journal of Neuroscience © 2011 Federation of European Neuroscience Societies and Blackwell Publishing Ltd http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.
spellingShingle Behavioral Neuroscience
McHugh, Stephen B
Fillenz, Marianne
Lowry, John P
Rawlins, J Nicolas P
Bannerman, David M
Brain tissue oxygen amperometry in behaving rats demonstrates functional dissociation of dorsal and ventral hippocampus during spatial processing and anxiety
title Brain tissue oxygen amperometry in behaving rats demonstrates functional dissociation of dorsal and ventral hippocampus during spatial processing and anxiety
title_full Brain tissue oxygen amperometry in behaving rats demonstrates functional dissociation of dorsal and ventral hippocampus during spatial processing and anxiety
title_fullStr Brain tissue oxygen amperometry in behaving rats demonstrates functional dissociation of dorsal and ventral hippocampus during spatial processing and anxiety
title_full_unstemmed Brain tissue oxygen amperometry in behaving rats demonstrates functional dissociation of dorsal and ventral hippocampus during spatial processing and anxiety
title_short Brain tissue oxygen amperometry in behaving rats demonstrates functional dissociation of dorsal and ventral hippocampus during spatial processing and anxiety
title_sort brain tissue oxygen amperometry in behaving rats demonstrates functional dissociation of dorsal and ventral hippocampus during spatial processing and anxiety
topic Behavioral Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3085075/
https://www.ncbi.nlm.nih.gov/pubmed/21105915
http://dx.doi.org/10.1111/j.1460-9568.2010.07497.x
work_keys_str_mv AT mchughstephenb braintissueoxygenamperometryinbehavingratsdemonstratesfunctionaldissociationofdorsalandventralhippocampusduringspatialprocessingandanxiety
AT fillenzmarianne braintissueoxygenamperometryinbehavingratsdemonstratesfunctionaldissociationofdorsalandventralhippocampusduringspatialprocessingandanxiety
AT lowryjohnp braintissueoxygenamperometryinbehavingratsdemonstratesfunctionaldissociationofdorsalandventralhippocampusduringspatialprocessingandanxiety
AT rawlinsjnicolasp braintissueoxygenamperometryinbehavingratsdemonstratesfunctionaldissociationofdorsalandventralhippocampusduringspatialprocessingandanxiety
AT bannermandavidm braintissueoxygenamperometryinbehavingratsdemonstratesfunctionaldissociationofdorsalandventralhippocampusduringspatialprocessingandanxiety