Multi-session transcranial direct current stimulation (tDCS) elicits inflammatory and regenerative processes in the rat brain.

Transcranial direct current stimulation (tDCS) is increasingly being used in human studies as an adjuvant tool to promote recovery of function after stroke. However, its neurobiological effects are still largely unknown. Electric fields are known to influence the migration of various cell types in v...

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Main Authors: Maria Adele Rueger, Meike Hedwig Keuters, Maureen Walberer, Ramona Braun, Rebecca Klein, Roland Sparing, Gereon Rudolf Fink, Rudolf Graf, Michael Schroeter
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3425495?pdf=render
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author Maria Adele Rueger
Meike Hedwig Keuters
Maureen Walberer
Ramona Braun
Rebecca Klein
Roland Sparing
Gereon Rudolf Fink
Rudolf Graf
Michael Schroeter
author_facet Maria Adele Rueger
Meike Hedwig Keuters
Maureen Walberer
Ramona Braun
Rebecca Klein
Roland Sparing
Gereon Rudolf Fink
Rudolf Graf
Michael Schroeter
author_sort Maria Adele Rueger
collection DOAJ
description Transcranial direct current stimulation (tDCS) is increasingly being used in human studies as an adjuvant tool to promote recovery of function after stroke. However, its neurobiological effects are still largely unknown. Electric fields are known to influence the migration of various cell types in vitro, but effects in vivo remain to be shown. Hypothesizing that tDCS might elicit the recruitment of cells to the cortex, we here studied the effects of tDCS in the rat brain in vivo. Adult Wistar rats (n = 16) were randomized to either anodal or cathodal stimulation for either 5 or 10 consecutive days (500 µA, 15 min). Bromodeoxyuridine (BrdU) was given systemically to label dividing cells throughout the experiment. Immunohistochemical analyses ex vivo included stainings for activated microglia and endogenous neural stem cells (NSC). Multi-session tDCS with the chosen parameters did not cause a cortical lesion. An innate immune response with early upregulation of Iba1-positive activated microglia occurred after both cathodal and anodal tDCS. The involvement of adaptive immunity as assessed by ICAM1-immunoreactivity was less pronounced. Most interestingly, only cathodal tDCS increased the number of endogenous NSC in the stimulated cortex. After 10 days of cathodal stimulation, proliferating NSC increased by ∼60%, with a significant effect of both polarity and number of tDCS sessions on the recruitment of NSC. We demonstrate a pro-inflammatory effect of both cathodal and anodal tDCS, and a polarity-specific migratory effect on endogenous NSC in vivo. Our data suggest that tDCS in human stroke patients might also elicit NSC activation and modulate neuroinflammation.
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spelling doaj.art-6f234b36ada64714b3a4af910d8fe4602022-12-21T19:08:34ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0178e4377610.1371/journal.pone.0043776Multi-session transcranial direct current stimulation (tDCS) elicits inflammatory and regenerative processes in the rat brain.Maria Adele RuegerMeike Hedwig KeutersMaureen WalbererRamona BraunRebecca KleinRoland SparingGereon Rudolf FinkRudolf GrafMichael SchroeterTranscranial direct current stimulation (tDCS) is increasingly being used in human studies as an adjuvant tool to promote recovery of function after stroke. However, its neurobiological effects are still largely unknown. Electric fields are known to influence the migration of various cell types in vitro, but effects in vivo remain to be shown. Hypothesizing that tDCS might elicit the recruitment of cells to the cortex, we here studied the effects of tDCS in the rat brain in vivo. Adult Wistar rats (n = 16) were randomized to either anodal or cathodal stimulation for either 5 or 10 consecutive days (500 µA, 15 min). Bromodeoxyuridine (BrdU) was given systemically to label dividing cells throughout the experiment. Immunohistochemical analyses ex vivo included stainings for activated microglia and endogenous neural stem cells (NSC). Multi-session tDCS with the chosen parameters did not cause a cortical lesion. An innate immune response with early upregulation of Iba1-positive activated microglia occurred after both cathodal and anodal tDCS. The involvement of adaptive immunity as assessed by ICAM1-immunoreactivity was less pronounced. Most interestingly, only cathodal tDCS increased the number of endogenous NSC in the stimulated cortex. After 10 days of cathodal stimulation, proliferating NSC increased by ∼60%, with a significant effect of both polarity and number of tDCS sessions on the recruitment of NSC. We demonstrate a pro-inflammatory effect of both cathodal and anodal tDCS, and a polarity-specific migratory effect on endogenous NSC in vivo. Our data suggest that tDCS in human stroke patients might also elicit NSC activation and modulate neuroinflammation.http://europepmc.org/articles/PMC3425495?pdf=render
spellingShingle Maria Adele Rueger
Meike Hedwig Keuters
Maureen Walberer
Ramona Braun
Rebecca Klein
Roland Sparing
Gereon Rudolf Fink
Rudolf Graf
Michael Schroeter
Multi-session transcranial direct current stimulation (tDCS) elicits inflammatory and regenerative processes in the rat brain.
PLoS ONE
title Multi-session transcranial direct current stimulation (tDCS) elicits inflammatory and regenerative processes in the rat brain.
title_full Multi-session transcranial direct current stimulation (tDCS) elicits inflammatory and regenerative processes in the rat brain.
title_fullStr Multi-session transcranial direct current stimulation (tDCS) elicits inflammatory and regenerative processes in the rat brain.
title_full_unstemmed Multi-session transcranial direct current stimulation (tDCS) elicits inflammatory and regenerative processes in the rat brain.
title_short Multi-session transcranial direct current stimulation (tDCS) elicits inflammatory and regenerative processes in the rat brain.
title_sort multi session transcranial direct current stimulation tdcs elicits inflammatory and regenerative processes in the rat brain
url http://europepmc.org/articles/PMC3425495?pdf=render
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