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运动小鼠血浆输注通过增加 3xTg-AD 小鼠海马神经可塑性和线粒体功能改善认知功能障碍。

Infusion of Plasma from Exercised Mice Ameliorates Cognitive Dysfunction by Increasing Hippocampal Neuroplasticity and Mitochondrial Functions in 3xTg-AD Mice.

机构信息

Exercise Rehabilitation Research Institute, Department of Exercise & Health Science, Sangmyung University, Seoul 03016, Korea.

Department of Physiology, College of Medicine, KyungHee University, Seoul 02447, Korea.

出版信息

Int J Mol Sci. 2020 May 6;21(9):3291. doi: 10.3390/ijms21093291.

DOI:10.3390/ijms21093291
PMID:32384696
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7247545/
Abstract

Alzheimer's disease is the most common neurodegenerative brain disease causing dementia. It is characterized by slow onset and gradual worsening of memory and other cognitive functions. Recently, parabiosis and infusion of plasma from young mice have been proposed to have positive effects in aging and Alzheimer's disease. Therefore, this study examined whether infusion of plasma from exercised mice improved cognitive functions related to the hippocampus in a 3xTg-Alzheimer's disease (AD) model. We collected plasma from young mice that had exercised for 3 months and injected 100 µL of plasma into the tail vein of 12-month-old 3xTg-AD mice 10 times at 3-day intervals. We then analyzed spatial learning and memory, long-term memory, hippocampal GSK3β/tau proteins, synaptic proteins, mitochondrial function, apoptosis, and neurogenesis. In the hippocampus of 3xTg-AD mice, infusion of plasma from exercised mice improved neuroplasticity and mitochondrial function and suppressed apoptosis, ultimately improving cognitive function. However, there was no improvement in tau hyperphosphorylation. This study showed that plasma from exercised mice could have a protective effect on cognitive dysfunction and neural circuits associated with AD via a tau-independent mechanism involving elevated brain-derived neurotrophic factor due to exercise.

摘要

阿尔茨海默病是最常见的神经退行性脑疾病,导致痴呆。其特征为记忆和其他认知功能缓慢发作和逐渐恶化。最近,共生和年轻小鼠的血浆输注被提出对衰老和阿尔茨海默病有积极影响。因此,本研究检查了在 3xTg-阿尔茨海默病(AD)模型中,输注来自运动小鼠的血浆是否能改善与海马体相关的认知功能。我们从运动了 3 个月的年轻小鼠中收集血浆,并在 3 天的间隔内,10 次将 100µL 血浆注入 12 个月大的 3xTg-AD 小鼠的尾静脉中。然后,我们分析了空间学习和记忆、长期记忆、海马体 GSK3β/tau 蛋白、突触蛋白、线粒体功能、细胞凋亡和神经发生。在 3xTg-AD 小鼠的海马体中,输注运动小鼠的血浆改善了神经可塑性和线粒体功能,并抑制了细胞凋亡,最终改善了认知功能。然而,tau 过度磷酸化没有得到改善。本研究表明,来自运动小鼠的血浆可能通过一种tau 非依赖性机制,由于运动导致脑源性神经营养因子升高,对与 AD 相关的认知功能障碍和神经回路具有保护作用。

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