Pikhovych Anton, Stolberg Nina Paloma, Jessica Flitsch Lea, Walter Helene Luise, Graf Rudolf, Fink Gereon Rudolf, Schroeter Michael, Rueger Maria Adele
Department of Neurology, University Hospital of Cologne, Kerpener Strasse 62, 50924 Cologne, Germany; Max Planck Institute for Metabolism Research, Gleueler Strasse 50, 50931 Cologne, Germany.
Department of Neurology, University Hospital of Cologne, Kerpener Strasse 62, 50924 Cologne, Germany.
Stem Cells Int. 2016;2016:2715196. doi: 10.1155/2016/2715196. Epub 2016 Jun 15.
Transcranial direct current stimulation (tDCS) has been suggested as an adjuvant tool to promote recovery of function after stroke, but the mechanisms of its action to date remain poorly understood. Moreover, studies aimed at unraveling those mechanisms have essentially been limited to the rat, where tDCS activates resident microglia as well as endogenous neural stem cells. Here we studied the effects of tDCS on microglia activation and neurogenesis in the mouse brain. Male wild-type mice were subjected to multisession tDCS of either anodal or cathodal polarity; sham-stimulated mice served as control. Activated microglia in the cerebral cortex and neuroblasts generated in the subventricular zone as the major neural stem cell niche were assessed immunohistochemically. Multisession tDCS at a sublesional charge density led to a polarity-dependent downregulation of the constitutive expression of Iba1 by microglia in the mouse cortex. In contrast, both anodal and, to an even greater extent, cathodal tDCS induced neurogenesis from the subventricular zone. Data suggest that tDCS elicits its action through multifacetted mechanisms, including immunomodulation and neurogenesis, and thus support the idea of using tDCS to induce regeneration and to promote recovery of function. Furthermore, data suggest that the effects of tDCS may be animal- and polarity-specific.
经颅直流电刺激(tDCS)已被提议作为促进中风后功能恢复的辅助工具,但迄今为止其作用机制仍知之甚少。此外,旨在阐明这些机制的研究基本上仅限于大鼠,在大鼠中,tDCS可激活常驻小胶质细胞以及内源性神经干细胞。在此,我们研究了tDCS对小鼠大脑中小胶质细胞激活和神经发生的影响。雄性野生型小鼠接受了阳极或阴极极性的多疗程tDCS;假刺激小鼠作为对照。通过免疫组织化学评估大脑皮层中活化的小胶质细胞以及作为主要神经干细胞生态位的脑室下区产生的神经母细胞。在亚损伤电荷密度下进行的多疗程tDCS导致小鼠皮层中小胶质细胞对Iba1组成型表达的极性依赖性下调。相反,阳极和更大程度上的阴极tDCS均诱导了脑室下区的神经发生。数据表明,tDCS通过多方面机制发挥作用,包括免疫调节和神经发生,因此支持使用tDCS诱导再生和促进功能恢复的观点。此外,数据表明tDCS的作用可能具有动物和极性特异性。