Trinchero Mariela F, Herrero Magalí, Mugnaini Matías, Aguilar-Arredondo Andrea, Benas Sabrina, Satorre Ignacio G, Kropff Emilio, Schinder Alejandro F
Laboratory of Neuronal Plasticity, Leloir Institute (IIBBA-CONICET); Buenos Aires, C1405BWE, Argentina.
Laboratory of Physiology and Algorithms of the Brain, Leloir Institute (IIBBA-CONICET); Buenos Aires, C1405BWE, Argentina.
bioRxiv. 2025 Jan 13:2025.01.13.632794. doi: 10.1101/2025.01.13.632794.
Gamma oscillations are disrupted in various neurological disorders, including Alzheimer's disease (AD). In AD mouse models, non-invasive audiovisual stimulation (AuViS) at 40 Hz enhances gamma oscillations, clears amyloid-beta, and improves cognition. We investigated mechanisms of circuit remodeling underlying these restorative effects by leveraging the sensitivity of hippocampal neurogenesis to activity in middle-aged wild-type mice. AuViS increased progenitor cell proliferation, neuronal differentiation and morphological maturation of newborn granule cells, promoting their synaptic integration. While visual or auditory stimuli alone induced dendritic growth, axonal changes required combined audiovisual stimulation. The actions of AuViS involved neurotrophin pathways, as shown by the lack of effect upon TrkB signaling blockade. These results reveal widespread plasticity mechanisms triggered by AuViS, a therapeutic approach currently proposed for treating neurological disorders in humans.
γ振荡在包括阿尔茨海默病(AD)在内的各种神经疾病中都会受到干扰。在AD小鼠模型中,40Hz的非侵入性视听刺激(AuViS)可增强γ振荡,清除β淀粉样蛋白,并改善认知能力。我们利用中年野生型小鼠海马神经发生对活动的敏感性,研究了这些恢复性作用背后的电路重塑机制。AuViS增加了祖细胞增殖、新生颗粒细胞的神经元分化和形态成熟,促进了它们的突触整合。虽然单独的视觉或听觉刺激会诱导树突生长,但轴突变化需要联合视听刺激。如对TrkB信号阻断缺乏效应所示,AuViS的作用涉及神经营养因子途径。这些结果揭示了由AuViS触发的广泛可塑性机制,AuViS是目前提出的一种治疗人类神经疾病的方法。