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Calcium imaging reveals glial involvement in transcranial direct current stimulation-induced plasticity in mouse brain

Transcranical direct current stimulation (tDCS) is a treatment known to ameliorate various neurological conditions and enhance memory and cognition in humans. tDCS has gained traction for its potential therapeutic value; however, little is known about its mechanism of action. Using a transgenic mous...

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Autores principales: Monai, Hiromu, Ohkura, Masamichi, Tanaka, Mika, Oe, Yuki, Konno, Ayumu, Hirai, Hirokazu, Mikoshiba, Katsuhiko, Itohara, Shigeyoshi, Nakai, Junichi, Iwai, Youichi, Hirase, Hajime
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4804173/
https://www.ncbi.nlm.nih.gov/pubmed/27000523
http://dx.doi.org/10.1038/ncomms11100
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author Monai, Hiromu
Ohkura, Masamichi
Tanaka, Mika
Oe, Yuki
Konno, Ayumu
Hirai, Hirokazu
Mikoshiba, Katsuhiko
Itohara, Shigeyoshi
Nakai, Junichi
Iwai, Youichi
Hirase, Hajime
author_facet Monai, Hiromu
Ohkura, Masamichi
Tanaka, Mika
Oe, Yuki
Konno, Ayumu
Hirai, Hirokazu
Mikoshiba, Katsuhiko
Itohara, Shigeyoshi
Nakai, Junichi
Iwai, Youichi
Hirase, Hajime
author_sort Monai, Hiromu
collection PubMed
description Transcranical direct current stimulation (tDCS) is a treatment known to ameliorate various neurological conditions and enhance memory and cognition in humans. tDCS has gained traction for its potential therapeutic value; however, little is known about its mechanism of action. Using a transgenic mouse expressing G-CaMP7 in astrocytes and a subpopulation of excitatory neurons, we find that tDCS induces large-amplitude astrocytic Ca(2+) surges across the entire cortex with no obvious changes in the local field potential. Moreover, sensory evoked cortical responses are enhanced after tDCS. These enhancements are dependent on the alpha-1 adrenergic receptor and are not observed in IP(3)R2 (inositol trisphosphate receptor type 2) knockout mice, in which astrocytic Ca(2+) surges are absent. Together, we propose that tDCS changes the metaplasticity of the cortex through astrocytic Ca(2+)/IP(3) signalling.
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spelling pubmed-48041732016-03-25 Calcium imaging reveals glial involvement in transcranial direct current stimulation-induced plasticity in mouse brain Monai, Hiromu Ohkura, Masamichi Tanaka, Mika Oe, Yuki Konno, Ayumu Hirai, Hirokazu Mikoshiba, Katsuhiko Itohara, Shigeyoshi Nakai, Junichi Iwai, Youichi Hirase, Hajime Nat Commun Article Transcranical direct current stimulation (tDCS) is a treatment known to ameliorate various neurological conditions and enhance memory and cognition in humans. tDCS has gained traction for its potential therapeutic value; however, little is known about its mechanism of action. Using a transgenic mouse expressing G-CaMP7 in astrocytes and a subpopulation of excitatory neurons, we find that tDCS induces large-amplitude astrocytic Ca(2+) surges across the entire cortex with no obvious changes in the local field potential. Moreover, sensory evoked cortical responses are enhanced after tDCS. These enhancements are dependent on the alpha-1 adrenergic receptor and are not observed in IP(3)R2 (inositol trisphosphate receptor type 2) knockout mice, in which astrocytic Ca(2+) surges are absent. Together, we propose that tDCS changes the metaplasticity of the cortex through astrocytic Ca(2+)/IP(3) signalling. Nature Publishing Group 2016-03-22 /pmc/articles/PMC4804173/ /pubmed/27000523 http://dx.doi.org/10.1038/ncomms11100 Text en Copyright © 2016, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. 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
Monai, Hiromu
Ohkura, Masamichi
Tanaka, Mika
Oe, Yuki
Konno, Ayumu
Hirai, Hirokazu
Mikoshiba, Katsuhiko
Itohara, Shigeyoshi
Nakai, Junichi
Iwai, Youichi
Hirase, Hajime
Calcium imaging reveals glial involvement in transcranial direct current stimulation-induced plasticity in mouse brain
title Calcium imaging reveals glial involvement in transcranial direct current stimulation-induced plasticity in mouse brain
title_full Calcium imaging reveals glial involvement in transcranial direct current stimulation-induced plasticity in mouse brain
title_fullStr Calcium imaging reveals glial involvement in transcranial direct current stimulation-induced plasticity in mouse brain
title_full_unstemmed Calcium imaging reveals glial involvement in transcranial direct current stimulation-induced plasticity in mouse brain
title_short Calcium imaging reveals glial involvement in transcranial direct current stimulation-induced plasticity in mouse brain
title_sort calcium imaging reveals glial involvement in transcranial direct current stimulation-induced plasticity in mouse brain
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4804173/
https://www.ncbi.nlm.nih.gov/pubmed/27000523
http://dx.doi.org/10.1038/ncomms11100
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