Electrical brain stimulation induces dendritic stripping but improves survival of silent neurons after optic nerve damage

Abstract Repetitive transorbital alternating current stimulation (rtACS) improves vision in patients with chronic visual impairments and an acute treatment increased survival of retinal neurons after optic nerve crush (ONC) in rodent models of visual system injury. However, despite this protection n...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Petra Henrich-Noack, Elena G. Sergeeva, Torben Eber, Qing You, Nadine Voigt, Jürgen Köhler, Sebastian Wagner, Stefanie Lazik, Christian Mawrin, Guihua Xu, Sayantan Biswas, Bernhard A. Sabel, Christopher Kai-Shun Leung
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2017
Materias:
R
Q
Acceso en línea:https://doaj.org/article/99340675faf845f2b6ab9a12b0e4221a
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:99340675faf845f2b6ab9a12b0e4221a
record_format dspace
spelling oai:doaj.org-article:99340675faf845f2b6ab9a12b0e4221a2021-12-02T12:30:17ZElectrical brain stimulation induces dendritic stripping but improves survival of silent neurons after optic nerve damage10.1038/s41598-017-00487-z2045-2322https://doaj.org/article/99340675faf845f2b6ab9a12b0e4221a2017-04-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-00487-zhttps://doaj.org/toc/2045-2322Abstract Repetitive transorbital alternating current stimulation (rtACS) improves vision in patients with chronic visual impairments and an acute treatment increased survival of retinal neurons after optic nerve crush (ONC) in rodent models of visual system injury. However, despite this protection no functional recovery could be detected in rats, which was interpreted as evidence of “silent survivor” cells. We now analysed the mechanisms underlying this “silent survival” effect. Using in vivo microscopy of the retina we investigated the survival and morphology of fluorescent neurons before and after ONC in animals receiving rtACS or sham treatment. One week after the crush, more neurons survived in the rtACS-treated group compared to sham-treated controls. In vivo imaging further revealed that in the initial post-ONC period, rtACS induced dendritic pruning in surviving neurons. In contrast, dendrites in untreated retinae degenerated slowly after the axonal trauma and neurons died. The complete loss of visual evoked potentials supports the hypothesis that cell signalling is abolished in the surviving neurons. Despite this evidence of “silencing”, intracellular free calcium imaging showed that the cells were still viable. We propose that early after trauma, complete dendritic stripping following rtACS protects neurons from excitotoxic cell death by silencing them.Petra Henrich-NoackElena G. SergeevaTorben EberQing YouNadine VoigtJürgen KöhlerSebastian WagnerStefanie LazikChristian MawrinGuihua XuSayantan BiswasBernhard A. SabelChristopher Kai-Shun LeungNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-13 (2017)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Petra Henrich-Noack
Elena G. Sergeeva
Torben Eber
Qing You
Nadine Voigt
Jürgen Köhler
Sebastian Wagner
Stefanie Lazik
Christian Mawrin
Guihua Xu
Sayantan Biswas
Bernhard A. Sabel
Christopher Kai-Shun Leung
Electrical brain stimulation induces dendritic stripping but improves survival of silent neurons after optic nerve damage
description Abstract Repetitive transorbital alternating current stimulation (rtACS) improves vision in patients with chronic visual impairments and an acute treatment increased survival of retinal neurons after optic nerve crush (ONC) in rodent models of visual system injury. However, despite this protection no functional recovery could be detected in rats, which was interpreted as evidence of “silent survivor” cells. We now analysed the mechanisms underlying this “silent survival” effect. Using in vivo microscopy of the retina we investigated the survival and morphology of fluorescent neurons before and after ONC in animals receiving rtACS or sham treatment. One week after the crush, more neurons survived in the rtACS-treated group compared to sham-treated controls. In vivo imaging further revealed that in the initial post-ONC period, rtACS induced dendritic pruning in surviving neurons. In contrast, dendrites in untreated retinae degenerated slowly after the axonal trauma and neurons died. The complete loss of visual evoked potentials supports the hypothesis that cell signalling is abolished in the surviving neurons. Despite this evidence of “silencing”, intracellular free calcium imaging showed that the cells were still viable. We propose that early after trauma, complete dendritic stripping following rtACS protects neurons from excitotoxic cell death by silencing them.
format article
author Petra Henrich-Noack
Elena G. Sergeeva
Torben Eber
Qing You
Nadine Voigt
Jürgen Köhler
Sebastian Wagner
Stefanie Lazik
Christian Mawrin
Guihua Xu
Sayantan Biswas
Bernhard A. Sabel
Christopher Kai-Shun Leung
author_facet Petra Henrich-Noack
Elena G. Sergeeva
Torben Eber
Qing You
Nadine Voigt
Jürgen Köhler
Sebastian Wagner
Stefanie Lazik
Christian Mawrin
Guihua Xu
Sayantan Biswas
Bernhard A. Sabel
Christopher Kai-Shun Leung
author_sort Petra Henrich-Noack
title Electrical brain stimulation induces dendritic stripping but improves survival of silent neurons after optic nerve damage
title_short Electrical brain stimulation induces dendritic stripping but improves survival of silent neurons after optic nerve damage
title_full Electrical brain stimulation induces dendritic stripping but improves survival of silent neurons after optic nerve damage
title_fullStr Electrical brain stimulation induces dendritic stripping but improves survival of silent neurons after optic nerve damage
title_full_unstemmed Electrical brain stimulation induces dendritic stripping but improves survival of silent neurons after optic nerve damage
title_sort electrical brain stimulation induces dendritic stripping but improves survival of silent neurons after optic nerve damage
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/99340675faf845f2b6ab9a12b0e4221a
work_keys_str_mv AT petrahenrichnoack electricalbrainstimulationinducesdendriticstrippingbutimprovessurvivalofsilentneuronsafteropticnervedamage
AT elenagsergeeva electricalbrainstimulationinducesdendriticstrippingbutimprovessurvivalofsilentneuronsafteropticnervedamage
AT torbeneber electricalbrainstimulationinducesdendriticstrippingbutimprovessurvivalofsilentneuronsafteropticnervedamage
AT qingyou electricalbrainstimulationinducesdendriticstrippingbutimprovessurvivalofsilentneuronsafteropticnervedamage
AT nadinevoigt electricalbrainstimulationinducesdendriticstrippingbutimprovessurvivalofsilentneuronsafteropticnervedamage
AT jurgenkohler electricalbrainstimulationinducesdendriticstrippingbutimprovessurvivalofsilentneuronsafteropticnervedamage
AT sebastianwagner electricalbrainstimulationinducesdendriticstrippingbutimprovessurvivalofsilentneuronsafteropticnervedamage
AT stefanielazik electricalbrainstimulationinducesdendriticstrippingbutimprovessurvivalofsilentneuronsafteropticnervedamage
AT christianmawrin electricalbrainstimulationinducesdendriticstrippingbutimprovessurvivalofsilentneuronsafteropticnervedamage
AT guihuaxu electricalbrainstimulationinducesdendriticstrippingbutimprovessurvivalofsilentneuronsafteropticnervedamage
AT sayantanbiswas electricalbrainstimulationinducesdendriticstrippingbutimprovessurvivalofsilentneuronsafteropticnervedamage
AT bernhardasabel electricalbrainstimulationinducesdendriticstrippingbutimprovessurvivalofsilentneuronsafteropticnervedamage
AT christopherkaishunleung electricalbrainstimulationinducesdendriticstrippingbutimprovessurvivalofsilentneuronsafteropticnervedamage
_version_ 1718394411180621824