Cargando…

Theta variation and spatiotemporal scaling along the septotemporal axis of the hippocampus

Hippocampal theta has been related to locomotor speed, attention, anxiety, sensorimotor integration and memory among other emergent phenomena. One difficulty in understanding the function of theta is that the hippocampus (HPC) modulates voluntary behavior at the same time that it processes sensory i...

Descripción completa

Detalles Bibliográficos
Autores principales: Long, Lauren L., Bunce, Jamie G., Chrobak, James J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4360780/
https://www.ncbi.nlm.nih.gov/pubmed/25852496
http://dx.doi.org/10.3389/fnsys.2015.00037
_version_ 1782361581682688000
author Long, Lauren L.
Bunce, Jamie G.
Chrobak, James J.
author_facet Long, Lauren L.
Bunce, Jamie G.
Chrobak, James J.
author_sort Long, Lauren L.
collection PubMed
description Hippocampal theta has been related to locomotor speed, attention, anxiety, sensorimotor integration and memory among other emergent phenomena. One difficulty in understanding the function of theta is that the hippocampus (HPC) modulates voluntary behavior at the same time that it processes sensory input. Both functions are correlated with characteristic changes in theta indices. The current review highlights a series of studies examining theta local field potential (LFP) signals across the septotemporal or longitudinal axis of the HPC. While the theta signal is coherent throughout the entirety of the HPC, the amplitude, but not the frequency, of theta varies significantly across its three-dimensional expanse. We suggest that the theta signal offers a rich vein of information about how distributed neuronal ensembles support emergent function. Further, we speculate that emergent function across the long axis varies with respect to spatiotemporal scale. Thus, septal HPC processes details of the proximal spatiotemporal environment while more temporal aspects process larger spaces and wider time-scales. The degree to which emergent functions are supported by the synchronization of theta across the septotemporal axis is an open question. Our working model is that theta synchrony serves to bind ensembles representing varying resolutions of spatiotemporal information at interdependent septotemporal areas of the HPC. Such synchrony and cooperative interactions along the septotemporal axis likely support memory formation and subsequent consolidation and retrieval.
format Online
Article
Text
id pubmed-4360780
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-43607802015-04-07 Theta variation and spatiotemporal scaling along the septotemporal axis of the hippocampus Long, Lauren L. Bunce, Jamie G. Chrobak, James J. Front Syst Neurosci Neuroscience Hippocampal theta has been related to locomotor speed, attention, anxiety, sensorimotor integration and memory among other emergent phenomena. One difficulty in understanding the function of theta is that the hippocampus (HPC) modulates voluntary behavior at the same time that it processes sensory input. Both functions are correlated with characteristic changes in theta indices. The current review highlights a series of studies examining theta local field potential (LFP) signals across the septotemporal or longitudinal axis of the HPC. While the theta signal is coherent throughout the entirety of the HPC, the amplitude, but not the frequency, of theta varies significantly across its three-dimensional expanse. We suggest that the theta signal offers a rich vein of information about how distributed neuronal ensembles support emergent function. Further, we speculate that emergent function across the long axis varies with respect to spatiotemporal scale. Thus, septal HPC processes details of the proximal spatiotemporal environment while more temporal aspects process larger spaces and wider time-scales. The degree to which emergent functions are supported by the synchronization of theta across the septotemporal axis is an open question. Our working model is that theta synchrony serves to bind ensembles representing varying resolutions of spatiotemporal information at interdependent septotemporal areas of the HPC. Such synchrony and cooperative interactions along the septotemporal axis likely support memory formation and subsequent consolidation and retrieval. Frontiers Media S.A. 2015-03-16 /pmc/articles/PMC4360780/ /pubmed/25852496 http://dx.doi.org/10.3389/fnsys.2015.00037 Text en Copyright © 2015 Long, Bunce and Chrobak. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution and reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Long, Lauren L.
Bunce, Jamie G.
Chrobak, James J.
Theta variation and spatiotemporal scaling along the septotemporal axis of the hippocampus
title Theta variation and spatiotemporal scaling along the septotemporal axis of the hippocampus
title_full Theta variation and spatiotemporal scaling along the septotemporal axis of the hippocampus
title_fullStr Theta variation and spatiotemporal scaling along the septotemporal axis of the hippocampus
title_full_unstemmed Theta variation and spatiotemporal scaling along the septotemporal axis of the hippocampus
title_short Theta variation and spatiotemporal scaling along the septotemporal axis of the hippocampus
title_sort theta variation and spatiotemporal scaling along the septotemporal axis of the hippocampus
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4360780/
https://www.ncbi.nlm.nih.gov/pubmed/25852496
http://dx.doi.org/10.3389/fnsys.2015.00037
work_keys_str_mv AT longlaurenl thetavariationandspatiotemporalscalingalongtheseptotemporalaxisofthehippocampus
AT buncejamieg thetavariationandspatiotemporalscalingalongtheseptotemporalaxisofthehippocampus
AT chrobakjamesj thetavariationandspatiotemporalscalingalongtheseptotemporalaxisofthehippocampus