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Theta Dynamics in Rat: Speed and Acceleration across the Septotemporal Axis

Theta (6–12 Hz) rhythmicity in the local field potential (LFP) reflects a clocking mechanism that brings physically isolated neurons together in time, allowing for the integration and segregation of distributed cell assemblies. Variation in the theta signal has been linked to locomotor speed, sensor...

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Autores principales: Long, Lauren L., Hinman, James R., Chen, Chi-Ming, Escabi, Monty A., Chrobak, James J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4026415/
https://www.ncbi.nlm.nih.gov/pubmed/24842406
http://dx.doi.org/10.1371/journal.pone.0097987
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author Long, Lauren L.
Hinman, James R.
Chen, Chi-Ming
Escabi, Monty A.
Chrobak, James J.
author_facet Long, Lauren L.
Hinman, James R.
Chen, Chi-Ming
Escabi, Monty A.
Chrobak, James J.
author_sort Long, Lauren L.
collection PubMed
description Theta (6–12 Hz) rhythmicity in the local field potential (LFP) reflects a clocking mechanism that brings physically isolated neurons together in time, allowing for the integration and segregation of distributed cell assemblies. Variation in the theta signal has been linked to locomotor speed, sensorimotor integration as well as cognitive processing. Previously, we have characterized the relationship between locomotor speed and theta power and how that relationship varies across the septotemporal (long) axis of the hippocampus (HPC). The current study investigated the relationship between whole body acceleration, deceleration and theta indices at CA1 and dentate gyrus (DG) sites along the septotemporal axis of the HPC in rats. Results indicate that whole body acceleration and deceleration predicts a significant amount of variability in the theta signal beyond variation in locomotor speed. Furthermore, deceleration was more predictive of variation in theta amplitude as compared to acceleration as rats traversed a linear track. Such findings highlight key variables that systematically predict the variability in the theta signal across the long axis of the HPC. A better understanding of the relative contribution of these quantifiable variables and their variation as a function of experience and environmental conditions should facilitate our understanding of the relationship between theta and sensorimotor/cognitive functions.
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spelling pubmed-40264152014-05-21 Theta Dynamics in Rat: Speed and Acceleration across the Septotemporal Axis Long, Lauren L. Hinman, James R. Chen, Chi-Ming Escabi, Monty A. Chrobak, James J. PLoS One Research Article Theta (6–12 Hz) rhythmicity in the local field potential (LFP) reflects a clocking mechanism that brings physically isolated neurons together in time, allowing for the integration and segregation of distributed cell assemblies. Variation in the theta signal has been linked to locomotor speed, sensorimotor integration as well as cognitive processing. Previously, we have characterized the relationship between locomotor speed and theta power and how that relationship varies across the septotemporal (long) axis of the hippocampus (HPC). The current study investigated the relationship between whole body acceleration, deceleration and theta indices at CA1 and dentate gyrus (DG) sites along the septotemporal axis of the HPC in rats. Results indicate that whole body acceleration and deceleration predicts a significant amount of variability in the theta signal beyond variation in locomotor speed. Furthermore, deceleration was more predictive of variation in theta amplitude as compared to acceleration as rats traversed a linear track. Such findings highlight key variables that systematically predict the variability in the theta signal across the long axis of the HPC. A better understanding of the relative contribution of these quantifiable variables and their variation as a function of experience and environmental conditions should facilitate our understanding of the relationship between theta and sensorimotor/cognitive functions. Public Library of Science 2014-05-19 /pmc/articles/PMC4026415/ /pubmed/24842406 http://dx.doi.org/10.1371/journal.pone.0097987 Text en © 2014 Long et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Long, Lauren L.
Hinman, James R.
Chen, Chi-Ming
Escabi, Monty A.
Chrobak, James J.
Theta Dynamics in Rat: Speed and Acceleration across the Septotemporal Axis
title Theta Dynamics in Rat: Speed and Acceleration across the Septotemporal Axis
title_full Theta Dynamics in Rat: Speed and Acceleration across the Septotemporal Axis
title_fullStr Theta Dynamics in Rat: Speed and Acceleration across the Septotemporal Axis
title_full_unstemmed Theta Dynamics in Rat: Speed and Acceleration across the Septotemporal Axis
title_short Theta Dynamics in Rat: Speed and Acceleration across the Septotemporal Axis
title_sort theta dynamics in rat: speed and acceleration across the septotemporal axis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4026415/
https://www.ncbi.nlm.nih.gov/pubmed/24842406
http://dx.doi.org/10.1371/journal.pone.0097987
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