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Optogenetic neuronal stimulation of the lateral cerebellar nucleus promotes persistent functional recovery after stroke

Stroke induces network-wide changes in the brain, affecting the excitability in both nearby and remotely connected regions. Brain stimulation is a promising neurorestorative technique that has been shown to improve stroke recovery by altering neuronal activity of the target area. However, it is uncl...

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Autores principales: Shah, Aatman M., Ishizaka, Shunsuke, Cheng, Michelle Y., Wang, Eric H., Bautista, Alex R., Levy, Sabrina, Smerin, Daniel, Sun, Guohua, Steinberg, Gary K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5451884/
https://www.ncbi.nlm.nih.gov/pubmed/28569261
http://dx.doi.org/10.1038/srep46612
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author Shah, Aatman M.
Ishizaka, Shunsuke
Cheng, Michelle Y.
Wang, Eric H.
Bautista, Alex R.
Levy, Sabrina
Smerin, Daniel
Sun, Guohua
Steinberg, Gary K.
author_facet Shah, Aatman M.
Ishizaka, Shunsuke
Cheng, Michelle Y.
Wang, Eric H.
Bautista, Alex R.
Levy, Sabrina
Smerin, Daniel
Sun, Guohua
Steinberg, Gary K.
author_sort Shah, Aatman M.
collection PubMed
description Stroke induces network-wide changes in the brain, affecting the excitability in both nearby and remotely connected regions. Brain stimulation is a promising neurorestorative technique that has been shown to improve stroke recovery by altering neuronal activity of the target area. However, it is unclear whether the beneficial effect of stimulation is a result of neuronal or non-neuronal activation, as existing stimulation techniques nonspecifically activate/inhibit all cell types (neurons, glia, endothelial cells, oligodendrocytes) in the stimulated area. Furthermore, which brain circuit is efficacious for brain stimulation is unknown. Here we use the optogenetics approach to selectively stimulate neurons in the lateral cerebellar nucleus (LCN), a deep cerebellar nucleus that sends major excitatory output to multiple motor and sensory areas in the forebrain. Repeated LCN stimulations resulted in a robust and persistent recovery on the rotating beam test, even after cessation of stimulations for 2 weeks. Furthermore, western blot analysis demonstrated that LCN stimulations significantly increased the axonal growth protein GAP43 in the ipsilesional somatosensory cortex. Our results demonstrate that pan-neuronal stimulations of the LCN is sufficient to promote robust and persistent recovery after stroke, and thus is a promising target for brain stimulation.
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spelling pubmed-54518842017-06-02 Optogenetic neuronal stimulation of the lateral cerebellar nucleus promotes persistent functional recovery after stroke Shah, Aatman M. Ishizaka, Shunsuke Cheng, Michelle Y. Wang, Eric H. Bautista, Alex R. Levy, Sabrina Smerin, Daniel Sun, Guohua Steinberg, Gary K. Sci Rep Article Stroke induces network-wide changes in the brain, affecting the excitability in both nearby and remotely connected regions. Brain stimulation is a promising neurorestorative technique that has been shown to improve stroke recovery by altering neuronal activity of the target area. However, it is unclear whether the beneficial effect of stimulation is a result of neuronal or non-neuronal activation, as existing stimulation techniques nonspecifically activate/inhibit all cell types (neurons, glia, endothelial cells, oligodendrocytes) in the stimulated area. Furthermore, which brain circuit is efficacious for brain stimulation is unknown. Here we use the optogenetics approach to selectively stimulate neurons in the lateral cerebellar nucleus (LCN), a deep cerebellar nucleus that sends major excitatory output to multiple motor and sensory areas in the forebrain. Repeated LCN stimulations resulted in a robust and persistent recovery on the rotating beam test, even after cessation of stimulations for 2 weeks. Furthermore, western blot analysis demonstrated that LCN stimulations significantly increased the axonal growth protein GAP43 in the ipsilesional somatosensory cortex. Our results demonstrate that pan-neuronal stimulations of the LCN is sufficient to promote robust and persistent recovery after stroke, and thus is a promising target for brain stimulation. Nature Publishing Group 2017-06-01 /pmc/articles/PMC5451884/ /pubmed/28569261 http://dx.doi.org/10.1038/srep46612 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Shah, Aatman M.
Ishizaka, Shunsuke
Cheng, Michelle Y.
Wang, Eric H.
Bautista, Alex R.
Levy, Sabrina
Smerin, Daniel
Sun, Guohua
Steinberg, Gary K.
Optogenetic neuronal stimulation of the lateral cerebellar nucleus promotes persistent functional recovery after stroke
title Optogenetic neuronal stimulation of the lateral cerebellar nucleus promotes persistent functional recovery after stroke
title_full Optogenetic neuronal stimulation of the lateral cerebellar nucleus promotes persistent functional recovery after stroke
title_fullStr Optogenetic neuronal stimulation of the lateral cerebellar nucleus promotes persistent functional recovery after stroke
title_full_unstemmed Optogenetic neuronal stimulation of the lateral cerebellar nucleus promotes persistent functional recovery after stroke
title_short Optogenetic neuronal stimulation of the lateral cerebellar nucleus promotes persistent functional recovery after stroke
title_sort optogenetic neuronal stimulation of the lateral cerebellar nucleus promotes persistent functional recovery after stroke
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5451884/
https://www.ncbi.nlm.nih.gov/pubmed/28569261
http://dx.doi.org/10.1038/srep46612
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