• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

运动训练与硫辛酸联合治疗对 NSE/APPsw 转基因小鼠阿尔茨海默病发病表型具有治疗作用。

The combination of exercise training and alpha-lipoic acid treatment has therapeutic effects on the pathogenic phenotypes of Alzheimer's disease in NSE/APPsw-transgenic mice.

机构信息

Exercise Biochemistry Laboratory, Korea National Sport University, Seoul 138-763, Korea.

出版信息

Int J Mol Med. 2010 Mar;25(3):337-46. doi: 10.3892/ijmm_00000350.

DOI:10.3892/ijmm_00000350
PMID:20127037
Abstract

Exercise training was suggested as a practical therapeutic strategy for human subjects suffering from Alzheimer's disease (AD) in our previous study. Therefore, the purpose of this study was to investigate the effects of combining exercise training with the administration of antioxidants on the pathological phenotype of AD. To accomplish this, non-transgenic mice (Non-Tg) and NSE/APPsw Tg mice were treated with alpha-lipoic acid and treadmill exercised for 16 weeks, after which their brains were evaluated to determine whether any changes in the pathological phenotype-related factors occurred. The results indicated that (i) the combination-applied (COMA) Tg group with exercise training (ET) and alpha-lipoic acid administration (LA) showed ameliorated spatial learning and memory compared to the sedentary (SED)-Tg and single-treatment groups; (ii) there were no differences in the level of Abeta-42 peptides across groups; (iii) the level of glucose transporter-1 and brain-derived neurotrophic factor proteins were highly increased in the COMA group, (iv) ET and LA did not induce a synergistic effect on the expression of heat shock protein-70 and apoptotic proteins including Bax and caspase-3; (v) the levels of SOD-1 and CAT suppressing oxidative stress were extensively higher in the COMA than in the single-treated groups and (vi) there were no significant differences across groups regarding these serum characteristics, although these levels were lower than the SED-Tg group. Taken together, these results suggest that the combination with ET and LA may contribute to protect the neuron injury induced by Abeta peptides and may be considered an effective therapeutic strategy for human subjects suffering from AD.

摘要

在我们之前的研究中,运动训练被建议作为治疗人类阿尔茨海默病(AD)患者的一种实用治疗策略。因此,本研究的目的是研究将运动训练与抗氧化剂给药相结合对 AD 的病理表型的影响。为此,我们使用非转基因(Non-Tg)和 NSE/APPsw Tg 小鼠,用α-硫辛酸和跑步机进行了 16 周的治疗,然后评估它们的大脑,以确定是否发生了与病理表型相关因素的变化。结果表明:(i)与运动训练(ET)和α-硫辛酸给药(LA)联合应用(COMA)Tg 组与久坐(SED)Tg 和单一治疗组相比,空间学习和记忆能力得到改善;(ii)各组之间β淀粉样肽(Abeta-42)的水平没有差异;(iii)COMA 组葡萄糖转运蛋白-1 和脑源性神经营养因子蛋白的水平显著升高;(iv)ET 和 LA 对热休克蛋白-70 和凋亡蛋白(包括 Bax 和 caspase-3)的表达没有协同作用;(v)COMA 组的超氧化物歧化酶-1(SOD-1)和过氧化氢酶(CAT)等抗氧化应激的水平显著高于单一治疗组;(vi)虽然这些水平低于 SED-Tg 组,但各组之间的这些血清特征没有差异。总之,这些结果表明,与 ET 和 LA 联合应用可能有助于保护 Abeta 肽诱导的神经元损伤,可被认为是治疗 AD 患者的有效治疗策略。

相似文献

1
The combination of exercise training and alpha-lipoic acid treatment has therapeutic effects on the pathogenic phenotypes of Alzheimer's disease in NSE/APPsw-transgenic mice.运动训练与硫辛酸联合治疗对 NSE/APPsw 转基因小鼠阿尔茨海默病发病表型具有治疗作用。
Int J Mol Med. 2010 Mar;25(3):337-46. doi: 10.3892/ijmm_00000350.
2
Exercise training acts as a therapeutic strategy for reduction of the pathogenic phenotypes for Alzheimer's disease in an NSE/APPsw-transgenic model.在NSE/APPsw转基因模型中,运动训练作为一种治疗策略,可减少阿尔茨海默病的致病表型。
Int J Mol Med. 2008 Oct;22(4):529-39.
3
The exosome of adipose-derived stem cells reduces β-amyloid pathology and apoptosis of neuronal cells derived from the transgenic mouse model of Alzheimer's disease.脂肪来源干细胞的外泌体可减轻阿尔茨海默病转基因小鼠模型来源神经元细胞的β-淀粉样蛋白病变和细胞凋亡。
Brain Res. 2018 Jul 15;1691:87-93. doi: 10.1016/j.brainres.2018.03.034. Epub 2018 Apr 3.
4
Alzheimer's phenotypes induced by overexpression of human presenilin 2 mutant proteins stimulate significant changes in key factors of glucose metabolism.人早老素 2 突变蛋白过表达诱导的阿尔茨海默病表型刺激葡萄糖代谢关键因素发生显著变化。
Mol Med Rep. 2013 May;7(5):1571-8. doi: 10.3892/mmr.2013.1404. Epub 2013 Mar 28.
5
Early changes in behavior deficits, amyloid beta-42 deposits and MAPK activation in doubly transgenic mice co-expressing NSE-controlled human mutant PS2 and APPsw.共表达NSE调控的人突变型PS2和APPsw的双转基因小鼠行为缺陷、β淀粉样蛋白42沉积和MAPK激活的早期变化
Cell Mol Neurobiol. 2005 Aug;25(5):881-98. doi: 10.1007/s10571-005-4950-x.
6
Running exercise delays neurodegeneration in amygdala and hippocampus of Alzheimer's disease (APP/PS1) transgenic mice.跑步运动可延缓阿尔茨海默病(APP/PS1)转基因小鼠杏仁核和海马体中的神经退行性变。
Neurobiol Learn Mem. 2015 Feb;118:189-97. doi: 10.1016/j.nlm.2014.12.005. Epub 2014 Dec 24.
7
Aberrant expressions of pathogenic phenotype in Alzheimer's diseased transgenic mice carrying NSE-controlled APPsw.携带NSE控制的APPsw的阿尔茨海默病转基因小鼠中致病表型的异常表达。
Exp Neurol. 2004 Mar;186(1):20-32. doi: 10.1016/j.expneurol.2003.09.021.
8
Treadmill exercise represses neuronal cell death in an aged transgenic mouse model of Alzheimer's disease.跑步机运动抑制阿尔茨海默病老年转基因小鼠模型中的神经元细胞死亡。
Neurosci Res. 2011 Feb;69(2):161-73. doi: 10.1016/j.neures.2010.10.004. Epub 2010 Oct 20.
9
Protective Effects of 2-Dodecyl-6-Methoxycyclohexa-2,5 -Diene-1,4-Dione Isolated from Averrhoa Carambola L. (Oxalidaceae) Roots on Neuron Apoptosis and Memory Deficits in Alzheimer's Disease.从阳桃(酢浆草科)根部分离出的2-十二烷基-6-甲氧基环己-2,5-二烯-1,4-二酮对阿尔茨海默病神经元凋亡和记忆缺陷的保护作用
Cell Physiol Biochem. 2018;49(3):1064-1073. doi: 10.1159/000493289. Epub 2018 Sep 7.
10
A spectrum of exercise training reduces soluble Aβ in a dose-dependent manner in a mouse model of Alzheimer's disease.运动训练谱以剂量依赖的方式降低阿尔茨海默病小鼠模型中的可溶性 Aβ。
Neurobiol Dis. 2016 Jan;85:218-224. doi: 10.1016/j.nbd.2015.11.004. Epub 2015 Nov 10.

引用本文的文献

1
Mapping the scientific research on exercise therapy for Alzheimer's disease: a scientometric study of hotspots and emerging trends.绘制关于阿尔茨海默病运动疗法的科学研究图谱:热点与新趋势的科学计量学研究
Front Aging Neurosci. 2025 Apr 3;17:1536515. doi: 10.3389/fnagi.2025.1536515. eCollection 2025.
2
The Effect of Physical Exercise on Patients With Mild Cognitive Impairment: A Scoping Review.体育锻炼对轻度认知障碍患者的影响:一项范围综述
Cureus. 2024 Nov 8;16(11):e73265. doi: 10.7759/cureus.73265. eCollection 2024 Nov.
3
Decoding molecular mechanisms: brain aging and Alzheimer's disease.
解码分子机制:大脑衰老与阿尔茨海默病
Neural Regen Res. 2025 Aug 1;20(8):2279-2299. doi: 10.4103/NRR.NRR-D-23-01403. Epub 2024 Jul 29.
4
Alpha-lipoic Acid: An Antioxidant with Anti-aging Properties for Disease Therapy.α-硫辛酸:一种具有抗衰老特性用于疾病治疗的抗氧化剂。
Curr Med Chem. 2025;32(1):23-54. doi: 10.2174/0109298673300496240416114827.
5
Effect of a combined program of running exercise and environmental enrichment on memory function and neurogenesis markers in amyloid-beta-induced Alzheimer-like model.跑步锻炼与环境富集联合方案对淀粉样蛋白诱导的阿尔茨海默病样模型中记忆功能和神经发生标志物的影响
Iran J Basic Med Sci. 2023;26(12):1400-1408. doi: 10.22038/IJBMS.2023.70269.15277.
6
Brain metabolism in Alzheimer's disease: biological mechanisms of exercise.阿尔茨海默病中的大脑代谢:运动的生物学机制。
Transl Neurodegener. 2023 Jun 26;12(1):33. doi: 10.1186/s40035-023-00364-y.
7
Non-Enzymatic Antioxidants against Alzheimer's Disease: Prevention, Diagnosis and Therapy.用于对抗阿尔茨海默病的非酶抗氧化剂:预防、诊断与治疗
Antioxidants (Basel). 2023 Jan 12;12(1):180. doi: 10.3390/antiox12010180.
8
Treadmill exercise promotes E3 ubiquitin ligase to remove amyloid β and P-tau and improve cognitive ability in APP/PS1 transgenic mice. treadmill 运动促进 E3 泛素连接酶去除淀粉样β和 P-tau 并改善 APP/PS1 转基因小鼠的认知能力。
J Neuroinflammation. 2022 Oct 4;19(1):243. doi: 10.1186/s12974-022-02607-7.
9
The Use of Bioactive Compounds in Hyperglycemia- and Amyloid Fibrils-Induced Toxicity in Type 2 Diabetes and Alzheimer's Disease.生物活性化合物在2型糖尿病和阿尔茨海默病中高血糖和淀粉样纤维诱导毒性中的应用
Pharmaceutics. 2022 Jan 20;14(2):235. doi: 10.3390/pharmaceutics14020235.
10
C-Phycocyanin-derived Phycocyanobilin as a Potential Nutraceutical Approach for Major Neurodegenerative Disorders and COVID-19- induced Damage to the Nervous System.藻蓝蛋白衍生的藻蓝胆素作为一种潜在的营养保健方法,可用于治疗主要神经退行性疾病和 COVID-19 引起的神经系统损伤。
Curr Neuropharmacol. 2021;19(12):2250-2275. doi: 10.2174/1570159X19666210408123807.