Abstract

BackgroundNeurogenesis is significantly impaired in the brains of both human patients and experimental animal models of Alzheimer’s disease (AD). Although deep brain stimulation promotes neurogenesis, it is an invasive technique that may damage neural circuitry along the path of the electrode. To circumvent this problem, we assessed whether intracranial electrical stimulation to the brain affects neurogenesis in a mouse model of Alzheimer’s disease (5xFAD).Methods and resultsWe used Ki67, Nestin, and doublecortin (DCX) as markers and determined that neurogenesis in both the subventricular zone (SVZ) and hippocampus were significantly reduced in the brains of 4-month-old 5xFAD mice. Guided by a finite element method (FEM) computer simulation to approximately estimate current and electric field in the mouse brain, electrodes were positioned on the skull that were likely to deliver stimulation to the SVZ and hippocampus. After a 4-week program of 40-Hz intracranial alternating current stimulation (iACS), neurogenesis indicated by expression of Ki67, Nestin, and DCX in both the SVZ and hippocampus were significantly increased compared to 5xFAD mice who received sham stimulation. The magnitude of neurogenesis was close to the wild-type (WT) age-matched unmanipulated controls.ConclusionOur results suggest that iACS is a promising, less invasive technique capable of effectively stimulating the SVZ and hippocampus regions in the mouse brain. Importantly, iACS can significantly boost neurogenesis in the brain and offers a potential treatment for AD.

Highlights

  • Neurogenesis is significantly impaired in the brains of both human patients and experimental animal models of Alzheimer’s disease (AD)

  • Our results suggest that intracranial alternating current stimulation (iACS) is a promising, less invasive technique capable of effectively stimulating the subventricular zone (SVZ) and hippocampus regions in the mouse brain

  • After a 4-week program of iACS (40 Hz), neurogenesis marked by Ki67, Nestin, and DCX in both the SVZ and hippocampus were significantly increased compared to The five-familial Alzheimer’s disease transgenic mouse model (5xFAD) mice who received sham stimulation

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Summary

Introduction

Neurogenesis is significantly impaired in the brains of both human patients and experimental animal models of Alzheimer’s disease (AD). Deep brain stimulation promotes neurogenesis, it is an invasive technique that may damage neural circuitry along the path of the electrode To circumvent this problem, we assessed whether intracranial electrical stimulation to the brain affects neurogenesis in a mouse model of Alzheimer’s disease (5xFAD). Recent improvements in fixation and labelling techniques have demonstrated abundant hippocampal neurogenesis in the healthy adult human brain [4, 13]. This neurogenesis is impaired in Alzheimer’s disease (AD), and as AD advances, the number and maturation of neurons decline progressively. Defective neurogenesis in the AD brain may implicate memory and other functional deficits

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