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Transcranial direct current stimulation promotes the mobility of engrafted NSCs in the rat brain

Authors :
Keuters, Meike Hedwig
Aswendt, Markus
Tennstaedt, Annette
Wiedermann, Dirk
Pikhovych, Anton
Rotthues, Steffen
Fink, Gereon Rudolf
Schroeter, Michael
Hoehn, Mathias
Rueger, Maria Adele
Keuters, Meike Hedwig
Aswendt, Markus
Tennstaedt, Annette
Wiedermann, Dirk
Pikhovych, Anton
Rotthues, Steffen
Fink, Gereon Rudolf
Schroeter, Michael
Hoehn, Mathias
Rueger, Maria Adele
Publication Year :
2015

Abstract

Transcranial direct current stimulation (tDCS) is used in numerous clinical studies and considered an effective and versatile add-on therapy in neurorehabilitation. To date, however, the underlying neurobiological mechanisms remain elusive. In a rat model of tDCS, we recently observed a polarity-dependent accumulation of endogenous neural stem cells (NSCs) in the stimulated cortex. Based upon these findings, we hypothesized that tDCS may exert a direct migratory effect on endogenous NSCs towards the stimulated cortex. Using noninvasive imaging, we here investigated whether tDCS may also cause a directed migration of engrafted NSCs. Murine NSCs were labeled with superparamagnetic particles of iron oxide (SPIOs) and implanted into rat striatum and corpus callosum. MRI was performed (i) immediately after implantation and (ii) after 10 tDCS sessions of anodal or cathodal polarity. Sham-stimulated rats served as control. Imaging results were validated ex vivo using immunohistochemistry. Overall migratory activity of NSCs almost doubled after anodal tDCS. However, no directed migration within the electric field (i.e. towards or away from the electrode) could be observed. Rather, an undirected outward migration from the center of the graft was detected. Xenograft transplantation induced a neuroinflammatory response that was significantly enhanced following cathodal tDCS. This inflammatory response did not impact negatively on the survival of implanted NSCs. Data suggest that anodal tDCS increases the undirected migratory activity of implanted NSCs. Since the electric field did not guide implanted NSCs over large distances, previously observed polarity-dependent accumulation of endogenous NSCs in the cortex might have originated from local proliferation. Results enhance our understanding of the neurobiological mechanisms underlying tDCS, and may thereby help to develop a targeted and sustainable application of tDCS in clinical practice. Copyright (c) 2014 John Wiley & Sons

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1247373289
Document Type :
Electronic Resource