在阿尔茨海默病小鼠模型中,40赫兹感觉干扰阻碍了癫痫的发生并减少了淀粉样蛋白病理。

IF 6.6 1区 医学 Q1 CLINICAL NEUROLOGY Epilepsia Pub Date : 2024-12-30 DOI:10.1111/epi.18222
Jennifer Tinston, Matthew R Hudson, Anna Harutyunyan, Zhibin Chen, Nigel C Jones
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引用次数: 0

摘要

目的:建立阿尔茨海默病(AD)小鼠5xFAD模型,重现了AD患者β -淀粉样蛋白(Aβ)沉积和明显的癫痫易感性。在AD模型中,40赫兹视听刺激是一种非侵入性技术,可以携带γ神经振荡,减少a β病理并调节胶质细胞表达。我们假设40hz的感觉刺激可以改善5xFAD小鼠的癫痫易感性,这可能与斑块减少和神经胶质表型调节有关。方法:5xFAD小鼠和野生型(WT)仔鼠接受1 h/d的40 hz视听刺激或假刺激(n = 7-11/组),从2周前开始持续到整个杏仁核点燃癫痫发生。死后分析包括星形胶质细胞和小胶质细胞的Aβ病理学和形态学。结果:与WT相比,5xFAD小鼠对癫痫发作的易感性增强,达到点燃终点的刺激较少(发病率比[IRR] = 1.46, p)。意义:在小鼠杏仁核点燃模型中,40赫兹感觉带束减缓了癫痫发生。虽然这种干预改善了5xFAD小鼠的Aβ病理,但观察到的抗癫痫作用也可能与对神经胶质细胞的影响有关,因为没有Aβ斑块的小鼠(即WT)也经历了干预的抗癫痫作用。
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Forty-hertz sensory entrainment impedes kindling epileptogenesis and reduces amyloid pathology in an Alzheimer disease mouse model.

Objective: The 5xFAD mouse model of Alzheimer disease (AD) recapitulates amyloid-beta (Aβ) deposition and pronounced seizure susceptibility observed in patients with AD. Forty-hertz audiovisual stimulation is a noninvasive technique that entrains gamma neural oscillations and can reduce Aβ pathology and modulate glial expression in AD models. We hypothesized that 40-Hz sensory stimulation would improve seizure susceptibility in 5xFAD mice and this would be associated with reduction of plaques and modulation of glial phenotypes.

Methods: 5xFAD mice and wild-type (WT) littermates received 1 h/day 40-Hz audiovisual stimulation or sham (n = 7-11/group), beginning 2 weeks before and continuing throughout amygdala kindling epileptogenesis. Postmortem analyses included Aβ pathology and morphology of astrocytes and microglia.

Results: 5xFAD mice exhibited enhanced susceptibility to seizures compared to WT, evidenced by fewer stimulations to reach kindling endpoint (incidence rate ratio [IRR] = 1.46, p < .0001) and a trend to higher seizure severity (odds ratio [OR] = .34, p = .059). Forty-hertz stimulation reduced the behavioral severity of the first seizure (OR = 4.04, p = .02) and delayed epileptogenesis, increasing the number of stimulations required to reach kindling endpoint (IRR = .82, p = .01) compared to sham, regardless of genotype. 5xFAD mice receiving sensory stimulation exhibited ~50% reduction in amyloid pathology compared to sham. Furthermore, markers of astrocytes and microglia were upregulated in both genotypes receiving 40-Hz stimulation.

Significance: Forty-hertz sensory entrainment slows epileptogenesis in the mouse amygdala kindling model. Although this intervention improves Aβ pathology in 5xFAD mice, the observed antiepileptogenic effect may also relate to effects on glia, because mice without Aβ plaques (i.e., WT) also experienced antiepileptogenic effects of the intervention.

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来源期刊
Epilepsia
Epilepsia 医学-临床神经学
CiteScore
10.90
自引率
10.70%
发文量
319
审稿时长
2-4 weeks
期刊介绍: Epilepsia is the leading, authoritative source for innovative clinical and basic science research for all aspects of epilepsy and seizures. In addition, Epilepsia publishes critical reviews, opinion pieces, and guidelines that foster understanding and aim to improve the diagnosis and treatment of people with seizures and epilepsy.
期刊最新文献
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