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운동이 초기 알츠하이머형 마우스의 산화성 스트레스와 열쇼크단백질에 미치는 영향Effects of Treadmill Running on Oxidative Stress and Heat Shock Protein in early stage of 3xTg-AD mice

Other Titles
Effects of Treadmill Running on Oxidative Stress and Heat Shock Protein in early stage of 3xTg-AD mice
Authors
강민정[강민정]조진경[조진경]
Issue Date
2019
Publisher
한국운동생리학회
Keywords
알츠하이머 병; 트레드밀 운동; 산화성 스트레스; 열쇼크 단백질; 3xTg-AD; Alzheimer’s disease; treadmill running; oxidative stress; heat shock protein; 3xTg-AD
Citation
운동과학, v.28, no.4, pp.381 - 387
Indexed
KCI
Journal Title
운동과학
Volume
28
Number
4
Start Page
381
End Page
387
URI
https://scholarworks.bwise.kr/skku/handle/2021.sw.skku/12381
ISSN
1226-1726
Abstract
PURPOSE: The mechanisms underlying the protective effects of exercise training against cognitive decline are not fully understood. This study aimed to investigate the effects of treadmill running on oxidative stress and heat shock protein levels in a mouse model of early stage triple transgenic Alzheimer’s disease (3xTg-AD). METHODS: We divided 5-month old 3xTg-AD mice (N=20) into the control (AD+CON, n=10) and exercise training (AD+EX, n=10) groups. Background strain mice were included as wild-type controls (WT, n=10). AD+EX mice were subjected to treadmill running at a speed of 15 m/min, 50 min/day, 5 days/week for 12 weeks. RESULTS: Treadmill running protected 3xTg-AD mice from cognitive decline and significantly suppressed the increase in soluble Aβ1-42 protein levels (AD+CON vs AD+EX, p=0.015) and the progression of oxidative damage. This was evidenced by significant increase in anti-oxidative protein levels such as superoxide dismutase-1 (SOD-1), heme oxygenase (HO-1) and heat shock protein 70 (HSP70) in the hippocampus of AD+EX mice compared to AD+CON mice. Moreover, the brain-derived neurotrophic factor (BDNF) and synaptic proteins such as PSD95 and synaptophysin were upregulated in AD+EX mice compared to AD+CON mice. CONCLUSIONS: Our findings support and extend previous studies reporting the preventive effects of exercise training on the pathological processes of the Alzheimer’s disease in the 3xTg AD mouse model.
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