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Dynamic synchronization between hippocampal representations and stepping

The hippocampus is a mammalian brain structure that expresses spatial representations(1) and is crucial for navigation(2,3). Navigation, in turn, intricately depends on locomotion; however, current accounts suggest a dissociation between hippocampal spatial representations and the details of locomot...

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Autores principales: Joshi, Abhilasha, Denovellis, Eric L., Mankili, Abhijith, Meneksedag, Yagiz, Davidson, Thomas J., Gillespie, Anna K., Guidera, Jennifer A., Roumis, Demetris, Frank, Loren M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10156593/
https://www.ncbi.nlm.nih.gov/pubmed/37046088
http://dx.doi.org/10.1038/s41586-023-05928-6
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author Joshi, Abhilasha
Denovellis, Eric L.
Mankili, Abhijith
Meneksedag, Yagiz
Davidson, Thomas J.
Gillespie, Anna K.
Guidera, Jennifer A.
Roumis, Demetris
Frank, Loren M.
author_facet Joshi, Abhilasha
Denovellis, Eric L.
Mankili, Abhijith
Meneksedag, Yagiz
Davidson, Thomas J.
Gillespie, Anna K.
Guidera, Jennifer A.
Roumis, Demetris
Frank, Loren M.
author_sort Joshi, Abhilasha
collection PubMed
description The hippocampus is a mammalian brain structure that expresses spatial representations(1) and is crucial for navigation(2,3). Navigation, in turn, intricately depends on locomotion; however, current accounts suggest a dissociation between hippocampal spatial representations and the details of locomotor processes. Specifically, the hippocampus is thought to represent mainly higher-order cognitive and locomotor variables such as position, speed and direction of movement(4–7), whereas the limb movements that propel the animal can be computed and represented primarily in subcortical circuits, including the spinal cord, brainstem and cerebellum(8–11). Whether hippocampal representations are actually decoupled from the detailed structure of locomotor processes remains unknown. To address this question, here we simultaneously monitored hippocampal spatial representations and ongoing limb movements underlying locomotion at fast timescales. We found that the forelimb stepping cycle in freely behaving rats is rhythmic and peaks at around 8 Hz during movement, matching the approximately 8 Hz modulation of hippocampal activity and spatial representations during locomotion(12). We also discovered precisely timed coordination between the time at which the forelimbs touch the ground (‘plant’ times of the stepping cycle) and the hippocampal representation of space. Notably, plant times coincide with hippocampal representations that are closest to the actual position of the nose of the rat, whereas between these plant times, the hippocampal representation progresses towards possible future locations. This synchronization was specifically detectable when rats approached spatial decisions. Together, our results reveal a profound and dynamic coordination on a timescale of tens of milliseconds between central cognitive representations and peripheral motor processes. This coordination engages and disengages rapidly in association with cognitive demands and is well suited to support rapid information exchange between cognitive and sensory–motor circuits.
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spelling pubmed-101565932023-05-05 Dynamic synchronization between hippocampal representations and stepping Joshi, Abhilasha Denovellis, Eric L. Mankili, Abhijith Meneksedag, Yagiz Davidson, Thomas J. Gillespie, Anna K. Guidera, Jennifer A. Roumis, Demetris Frank, Loren M. Nature Article The hippocampus is a mammalian brain structure that expresses spatial representations(1) and is crucial for navigation(2,3). Navigation, in turn, intricately depends on locomotion; however, current accounts suggest a dissociation between hippocampal spatial representations and the details of locomotor processes. Specifically, the hippocampus is thought to represent mainly higher-order cognitive and locomotor variables such as position, speed and direction of movement(4–7), whereas the limb movements that propel the animal can be computed and represented primarily in subcortical circuits, including the spinal cord, brainstem and cerebellum(8–11). Whether hippocampal representations are actually decoupled from the detailed structure of locomotor processes remains unknown. To address this question, here we simultaneously monitored hippocampal spatial representations and ongoing limb movements underlying locomotion at fast timescales. We found that the forelimb stepping cycle in freely behaving rats is rhythmic and peaks at around 8 Hz during movement, matching the approximately 8 Hz modulation of hippocampal activity and spatial representations during locomotion(12). We also discovered precisely timed coordination between the time at which the forelimbs touch the ground (‘plant’ times of the stepping cycle) and the hippocampal representation of space. Notably, plant times coincide with hippocampal representations that are closest to the actual position of the nose of the rat, whereas between these plant times, the hippocampal representation progresses towards possible future locations. This synchronization was specifically detectable when rats approached spatial decisions. Together, our results reveal a profound and dynamic coordination on a timescale of tens of milliseconds between central cognitive representations and peripheral motor processes. This coordination engages and disengages rapidly in association with cognitive demands and is well suited to support rapid information exchange between cognitive and sensory–motor circuits. Nature Publishing Group UK 2023-04-12 2023 /pmc/articles/PMC10156593/ /pubmed/37046088 http://dx.doi.org/10.1038/s41586-023-05928-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Joshi, Abhilasha
Denovellis, Eric L.
Mankili, Abhijith
Meneksedag, Yagiz
Davidson, Thomas J.
Gillespie, Anna K.
Guidera, Jennifer A.
Roumis, Demetris
Frank, Loren M.
Dynamic synchronization between hippocampal representations and stepping
title Dynamic synchronization between hippocampal representations and stepping
title_full Dynamic synchronization between hippocampal representations and stepping
title_fullStr Dynamic synchronization between hippocampal representations and stepping
title_full_unstemmed Dynamic synchronization between hippocampal representations and stepping
title_short Dynamic synchronization between hippocampal representations and stepping
title_sort dynamic synchronization between hippocampal representations and stepping
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10156593/
https://www.ncbi.nlm.nih.gov/pubmed/37046088
http://dx.doi.org/10.1038/s41586-023-05928-6
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