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听觉或视听刺激可改善载脂蛋白 E4 敲入小鼠的认知障碍和神经病理学。

Auditory or Audiovisual Stimulation Ameliorates Cognitive Impairment and Neuropathology in ApoE4 Knock-In Mice.

机构信息

Institute of New Frontier Research Team, College of Medicine, Hallym University, Chuncheon 24252, Republic of Korea.

Department of Neurology, Chuncheon Sacred Heart Hospital, Hallym University College of Medicine, Chuncheon 24252, Republic of Korea.

出版信息

Int J Mol Sci. 2023 Jan 4;24(2):938. doi: 10.3390/ijms24020938.

DOI:10.3390/ijms24020938
PMID:36674449
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9863367/
Abstract

We hypothesized that auditory stimulation could reduce the progression of Alzheimer’s disease (AD), and that audiovisual stimulation could have additional effects through multisensory integration. We exposed 12 month old Apoetm1.1(APOE*4)Adiuj mice (a mouse model of sporadic AD) to auditory (A) or audiovisual stimulation (AV) at 40 Hz for 14 days in a soundproof chamber system (no stimulation, N). Behavioral tests were performed before and after each session, and their brain tissues were assessed for amyloid-beta expression and apoptotic cell death, after 14 days. Furthermore, brain levels of acetylcholine and apoptosis-related proteins were analyzed. In the Y-maze test, the percentage relative alternation was significantly higher in group A than in group N mice. Amyloid-beta and TUNEL positivity in the hippocampal CA3 region was significantly lower in group A and group AV mice than in group N mice (p < 0.05). Acetylcholine levels were significantly higher in group A and group AV mice than in group N mice (p < 0.05). Compared to group N mice, expression of the proapoptotic proteins Bax and caspase-3 was lower in group A, and expression of the antiapoptotic protein Bcl-2 was higher in group AV. In a mouse model of early-stage sporadic AD, auditory or audiovisual stimulation improved cognitive performance and neuropathology.

摘要

我们假设听觉刺激可以减缓阿尔茨海默病(AD)的进展,而视听刺激可以通过多感官整合产生额外的效果。我们将 12 个月大的 Apoetm1.1(APOE*4)Adiuj 小鼠(一种散发性 AD 的小鼠模型)暴露于隔音室系统中的听觉(A)或视听刺激(AV)40 Hz 下 14 天(无刺激,N)。在每次治疗前后进行行为测试,并在 14 天后评估其脑组织中淀粉样β表达和凋亡细胞死亡情况。此外,还分析了脑内乙酰胆碱和凋亡相关蛋白的水平。在 Y 迷宫测试中,A 组的相对交替百分比明显高于 N 组。A 组和 AV 组的海马 CA3 区的淀粉样β和 TUNEL 阳性率明显低于 N 组(p<0.05)。A 组和 AV 组的乙酰胆碱水平明显高于 N 组(p<0.05)。与 N 组相比,A 组促凋亡蛋白 Bax 和 caspase-3 的表达较低,而抗凋亡蛋白 Bcl-2 的表达在 AV 组较高。在早期散发性 AD 的小鼠模型中,听觉或视听刺激改善了认知表现和神经病理学。

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