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Specific Increase of Hippocampal Delta Oscillations Across Consecutive Treadmill Runs

Running speed affects theta (6–10 Hz) oscillations, the most prominent rhythm in the rat hippocampus. Many reports have found a strong positive correlation between locomotion speed and the amplitude and frequency of theta oscillations. However, less is known about how other rhythms such as delta (0....

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Autores principales: Furtunato, Alan M. B., Lobão-Soares, Bruno, Tort, Adriano Bretanha Lopes, Belchior, Hindiael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7333663/
https://www.ncbi.nlm.nih.gov/pubmed/32676013
http://dx.doi.org/10.3389/fnbeh.2020.00101
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author Furtunato, Alan M. B.
Lobão-Soares, Bruno
Tort, Adriano Bretanha Lopes
Belchior, Hindiael
author_facet Furtunato, Alan M. B.
Lobão-Soares, Bruno
Tort, Adriano Bretanha Lopes
Belchior, Hindiael
author_sort Furtunato, Alan M. B.
collection PubMed
description Running speed affects theta (6–10 Hz) oscillations, the most prominent rhythm in the rat hippocampus. Many reports have found a strong positive correlation between locomotion speed and the amplitude and frequency of theta oscillations. However, less is known about how other rhythms such as delta (0.5–4 Hz) and gamma (25–100 Hz) are affected, and how consecutive runs impact oscillatory activity in hippocampal networks. Here, we investigated whether the successive execution of short-term runs modulates local field potentials (LFPs) in the rat hippocampus. To do this, we trained Long-Evans rats to perform voluntary 15-s runs at 30 cm/s on a treadmill placed on the central stem of an eight-shape maze, in which they subsequently performed a spatial alternation task. We bilaterally recorded CA1 LFPs while rats executed at least 35 runs on the treadmill-maze apparatus. Within running periods, we observed progressive increases in delta band power along with decreases in the power of the theta and gamma bands across runs. Concurrently, the inter-hemispheric phase coherence in the delta band significantly increased, while in the theta and gamma bands exhibited no changes. Delta power and inter-hemispheric coherence correlated better with the trial number than with the actual running speed. We observed no significant differences in running speed, head direction, nor in spatial occupancy across runs. Our results thus show that consecutive treadmill runs at the same speed positively modulates the power and coherence of delta oscillations in the rat hippocampus.
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spelling pubmed-73336632020-07-15 Specific Increase of Hippocampal Delta Oscillations Across Consecutive Treadmill Runs Furtunato, Alan M. B. Lobão-Soares, Bruno Tort, Adriano Bretanha Lopes Belchior, Hindiael Front Behav Neurosci Neuroscience Running speed affects theta (6–10 Hz) oscillations, the most prominent rhythm in the rat hippocampus. Many reports have found a strong positive correlation between locomotion speed and the amplitude and frequency of theta oscillations. However, less is known about how other rhythms such as delta (0.5–4 Hz) and gamma (25–100 Hz) are affected, and how consecutive runs impact oscillatory activity in hippocampal networks. Here, we investigated whether the successive execution of short-term runs modulates local field potentials (LFPs) in the rat hippocampus. To do this, we trained Long-Evans rats to perform voluntary 15-s runs at 30 cm/s on a treadmill placed on the central stem of an eight-shape maze, in which they subsequently performed a spatial alternation task. We bilaterally recorded CA1 LFPs while rats executed at least 35 runs on the treadmill-maze apparatus. Within running periods, we observed progressive increases in delta band power along with decreases in the power of the theta and gamma bands across runs. Concurrently, the inter-hemispheric phase coherence in the delta band significantly increased, while in the theta and gamma bands exhibited no changes. Delta power and inter-hemispheric coherence correlated better with the trial number than with the actual running speed. We observed no significant differences in running speed, head direction, nor in spatial occupancy across runs. Our results thus show that consecutive treadmill runs at the same speed positively modulates the power and coherence of delta oscillations in the rat hippocampus. Frontiers Media S.A. 2020-06-23 /pmc/articles/PMC7333663/ /pubmed/32676013 http://dx.doi.org/10.3389/fnbeh.2020.00101 Text en Copyright © 2020 Furtunato, Lobão-Soares, Tort and Belchior. 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 or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) 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
Furtunato, Alan M. B.
Lobão-Soares, Bruno
Tort, Adriano Bretanha Lopes
Belchior, Hindiael
Specific Increase of Hippocampal Delta Oscillations Across Consecutive Treadmill Runs
title Specific Increase of Hippocampal Delta Oscillations Across Consecutive Treadmill Runs
title_full Specific Increase of Hippocampal Delta Oscillations Across Consecutive Treadmill Runs
title_fullStr Specific Increase of Hippocampal Delta Oscillations Across Consecutive Treadmill Runs
title_full_unstemmed Specific Increase of Hippocampal Delta Oscillations Across Consecutive Treadmill Runs
title_short Specific Increase of Hippocampal Delta Oscillations Across Consecutive Treadmill Runs
title_sort specific increase of hippocampal delta oscillations across consecutive treadmill runs
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7333663/
https://www.ncbi.nlm.nih.gov/pubmed/32676013
http://dx.doi.org/10.3389/fnbeh.2020.00101
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