Bilateral transcranial direct‐current stimulation promotes migration of subventricular zone‐derived neuroblasts toward ischemic brain

Author:

Lei Ruixue12,Wang Shu2,Liu Anchun2,Cheng Jing2,Zhang Zhifeng2,Ren Jinyang3,Yao Xujin3,Kong Xiangyi3,Ma Wenlong3,Che Fengyuan4,Chen Juan5,Wan Qi236ORCID

Affiliation:

1. Department of Pathology, Anyang Tumour Hospital The Affiliated Anyang Tumor Hospital of Henan University of Science and Technology Anyang Henan China

2. Department of Physiology, School of Medicine Wuhan University Wuhan China

3. Institute of Neuroregeneration & Neurorehabilitation, Department of Neurosurgery Qingdao University Qingdao China

4. Central Laboratory, Department of Neurology Linyi People's Hospital, Qingdao University Linyi Shandong China

5. Department of Neurology, the Central Hospital of Wuhan tongji medical collof Huazhong University of Science & Technology Wuhan China

6. Qingdao Gui‐Hong Intelligent Medical Technology Co. Ltd Qingdao China

Abstract

AbstractIschemic insult stimulates proliferation of neural stem cells (NSCs) in the subventricular zone (SVZ) after stroke. However, only a fraction of NSC‐derived neuroblasts from SVZ migrate toward poststroke brain region. We have previously reported that direct‐current stimulation guides NSC migration toward the cathode in vitro. Accordingly, we set up a new method of transcranial direct‐current stimulation (tDCS), in which the cathodal electrode is placed on the ischemic hemisphere and anodal electrode on the contralateral hemisphere of rats subjected to ischemia–reperfusion injury. We show that the application of this bilateral tDCS (BtDCS) promotes the migration of NSC‐derived neuroblasts from SVZ toward the cathode direction into poststroke striatum. Reversing the position of the electrodes blocks the effect of BtDCS on the migration of neuroblasts from SVZ. BtDCS protects against neuronal death and improves the functional recovery of stroke animals. Thus, the migration of NSC‐derived neuroblasts from SVZ toward poststroke brain region contributes to the effect of BtDCS against ischemia‐induced neuronal death, supporting a potential development of noninvasive BtDCS as an endogenous neurogenesis‐based stroke therapy.

Publisher

Wiley

Subject

Cancer Research,Biochemistry, Genetics and Molecular Biology (miscellaneous),Molecular Medicine,Physiology

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