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Anodal transcranial direct current stimulation boosts synaptic plasticity and memory in mice via epigenetic regulation of Bdnf expression

机译:阳极经颅直流电刺激通过Bdnf表达的表观遗传调控来增强小鼠的突触可塑性和记忆力

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摘要

The effects of transcranial direct current stimulation (tDCS) on brain functions and the underlying molecular mechanisms are yet largely unknown. Here we report that mice subjected to 20-min anodal tDCS exhibited one-week lasting increases in hippocampal LTP, learning and memory. These effects were associated with enhanced: i) acetylation of brain-derived neurotrophic factor (Bdnf) promoter I; ii) expression of Bdnf exons I and IX; iii) Bdnf protein levels. The hippocampi of stimulated mice also exhibited enhanced CREB phosphorylation, pCREB binding to Bdnf promoter I and recruitment of CBP on the same regulatory sequence. Inhibition of acetylation and blockade of TrkB receptors hindered tDCS effects at molecular, electrophysiological and behavioral levels. Collectively, our findings suggest that anodal tDCS increases hippocampal LTP and memory via chromatin remodeling of Bdnf regulatory sequences leading to increased expression of this gene, and support the therapeutic potential of tDCS for brain diseases associated with impaired neuroplasticity.
机译:经颅直流电刺激(tDCS)对脑功能和潜在的分子机制的影响尚不清楚。在这里,我们报告老鼠接受20分钟的阳极tDCS表现出海马LTP,学习和记忆的持续持续一星期。这些作用与增强有关:i)脑源性神经营养因子(Bdnf)启动子I的乙酰化; ii)Bdnf外显子I和IX的表达; iii)Bdnf蛋白水平。受刺激的小鼠的海马体还表现出增强的CREB磷酸化,pCREB与Bdnf启动子I的结合以及CBP在相同调控序列上的募集。在分子,电生理和行为水平上抑制乙酰化和阻断TrkB受体阻碍了tDCS的作用。总体而言,我们的发现表明,阳极tDCS通过Bdnf调控序列的染色质重塑导致海马LTP和记忆增强,从而导致该基因表达增加,并支持tDCS在与神经可塑性受损相关的脑部疾病中的治疗潜力。

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