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Cerebrocortical activation following unilateral labyrinthectomy in mice characterized by whole-brain clearing: implications for sensory reweighting

Posture and gait are maintained by sensory inputs from the vestibular, visual, and somatosensory systems and motor outputs. Upon vestibular damage, the visual and/or somatosensory systems functionally substitute by cortical mechanisms called “sensory reweighting”. We investigated the cerebrocortical...

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Autores principales: Kai, Ryota, Takahashi, Kuniyuki, Tainaka, Kazuki, Iwakura, Yuriko, Namba, Hisaaki, Saito, Nae, Sasaoka, Toshikuni, Yamaguchi, Shun, Nawa, Hiroyuki, Horii, Arata
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9474865/
https://www.ncbi.nlm.nih.gov/pubmed/36104440
http://dx.doi.org/10.1038/s41598-022-19678-4
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author Kai, Ryota
Takahashi, Kuniyuki
Tainaka, Kazuki
Iwakura, Yuriko
Namba, Hisaaki
Saito, Nae
Sasaoka, Toshikuni
Yamaguchi, Shun
Nawa, Hiroyuki
Horii, Arata
author_facet Kai, Ryota
Takahashi, Kuniyuki
Tainaka, Kazuki
Iwakura, Yuriko
Namba, Hisaaki
Saito, Nae
Sasaoka, Toshikuni
Yamaguchi, Shun
Nawa, Hiroyuki
Horii, Arata
author_sort Kai, Ryota
collection PubMed
description Posture and gait are maintained by sensory inputs from the vestibular, visual, and somatosensory systems and motor outputs. Upon vestibular damage, the visual and/or somatosensory systems functionally substitute by cortical mechanisms called “sensory reweighting”. We investigated the cerebrocortical mechanisms underlying sensory reweighting after unilateral labyrinthectomy (UL) in mice. Arc-dVenus transgenic mice, in which the gene encoding the fluorescent protein dVenus is transcribed under the control of the promoter of the immediate early gene Arc, were used in combination with whole-brain three-dimensional (3D) imaging. Performance on the rotarod was measured as a behavioral correlate of sensory reweighting. Following left UL, all mice showed the head roll-tilt until UL10, indicating the vestibular periphery damage. The rotarod performance worsened in the UL mice from UL1 to UL3, which rapidly recovered. Whole-brain 3D imaging revealed that the number of activated neurons in S1, but not in V1, in UL7 was higher than that in sham-treated mice. At UL7, medial prefrontal cortex (mPFC) and agranular insular cortex (AIC) activation was also observed. Therefore, sensory reweighting to the somatosensory system could compensate for vestibular dysfunction following UL; further, mPFC and AIC contribute to the integration of sensory and motor functions to restore balance.
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spelling pubmed-94748652022-09-16 Cerebrocortical activation following unilateral labyrinthectomy in mice characterized by whole-brain clearing: implications for sensory reweighting Kai, Ryota Takahashi, Kuniyuki Tainaka, Kazuki Iwakura, Yuriko Namba, Hisaaki Saito, Nae Sasaoka, Toshikuni Yamaguchi, Shun Nawa, Hiroyuki Horii, Arata Sci Rep Article Posture and gait are maintained by sensory inputs from the vestibular, visual, and somatosensory systems and motor outputs. Upon vestibular damage, the visual and/or somatosensory systems functionally substitute by cortical mechanisms called “sensory reweighting”. We investigated the cerebrocortical mechanisms underlying sensory reweighting after unilateral labyrinthectomy (UL) in mice. Arc-dVenus transgenic mice, in which the gene encoding the fluorescent protein dVenus is transcribed under the control of the promoter of the immediate early gene Arc, were used in combination with whole-brain three-dimensional (3D) imaging. Performance on the rotarod was measured as a behavioral correlate of sensory reweighting. Following left UL, all mice showed the head roll-tilt until UL10, indicating the vestibular periphery damage. The rotarod performance worsened in the UL mice from UL1 to UL3, which rapidly recovered. Whole-brain 3D imaging revealed that the number of activated neurons in S1, but not in V1, in UL7 was higher than that in sham-treated mice. At UL7, medial prefrontal cortex (mPFC) and agranular insular cortex (AIC) activation was also observed. Therefore, sensory reweighting to the somatosensory system could compensate for vestibular dysfunction following UL; further, mPFC and AIC contribute to the integration of sensory and motor functions to restore balance. Nature Publishing Group UK 2022-09-14 /pmc/articles/PMC9474865/ /pubmed/36104440 http://dx.doi.org/10.1038/s41598-022-19678-4 Text en © The Author(s) 2022 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
Kai, Ryota
Takahashi, Kuniyuki
Tainaka, Kazuki
Iwakura, Yuriko
Namba, Hisaaki
Saito, Nae
Sasaoka, Toshikuni
Yamaguchi, Shun
Nawa, Hiroyuki
Horii, Arata
Cerebrocortical activation following unilateral labyrinthectomy in mice characterized by whole-brain clearing: implications for sensory reweighting
title Cerebrocortical activation following unilateral labyrinthectomy in mice characterized by whole-brain clearing: implications for sensory reweighting
title_full Cerebrocortical activation following unilateral labyrinthectomy in mice characterized by whole-brain clearing: implications for sensory reweighting
title_fullStr Cerebrocortical activation following unilateral labyrinthectomy in mice characterized by whole-brain clearing: implications for sensory reweighting
title_full_unstemmed Cerebrocortical activation following unilateral labyrinthectomy in mice characterized by whole-brain clearing: implications for sensory reweighting
title_short Cerebrocortical activation following unilateral labyrinthectomy in mice characterized by whole-brain clearing: implications for sensory reweighting
title_sort cerebrocortical activation following unilateral labyrinthectomy in mice characterized by whole-brain clearing: implications for sensory reweighting
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9474865/
https://www.ncbi.nlm.nih.gov/pubmed/36104440
http://dx.doi.org/10.1038/s41598-022-19678-4
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