Advance of sporadic Alzheimer's disease animal models

被引:79
作者
Zhang, Lili [1 ]
Chen, Chen [1 ]
Mak, Marvin S. H. [2 ]
Lu, Junfeng [1 ]
Wu, Zeqing [1 ]
Chen, Qiuhe [1 ]
Han, Yifan [2 ,3 ,4 ]
Li, Yuefeng [5 ]
Pi, Rongbiao [1 ,3 ,6 ,7 ]
机构
[1] Sun Yat Sen Univ, Sch Pharmaceut Sci, Guangzhou 510006, Guangdong, Peoples R China
[2] Hong Kong Polytech Univ, Inst Modern Chinese Med, Dept Appl Biol & Chem Technol, Hung Hom, Hong Kong, Peoples R China
[3] Lnternatl Joint Lab SYSU PolyU HK Novel Antidemen, Guangzhou, Guangdong, Peoples R China
[4] Hong Kong Polytech Univ Shenzhen Res Inst, State Key Lab Chinese Med & Mol Pharmacol Incubat, Shenzhen Res Inst, Shenzhen, Peoples R China
[5] Guangdong Landau Biotechnol Co Ltd, Guangzhou, Guangdong, Peoples R China
[6] Sun Yat Sen Univ, Natl & Local United Engn Lab Druggabil & New Drug, Guangzhou, Guangdong, Peoples R China
[7] Sun Yat Sen Univ, Zhongshan Sch Med, Guangdong Prov Key Lab Brain Funct & Dis, Guangzhou, Guangdong, Peoples R China
关键词
animal model; mechanism; sporadic Alzheimer's disease; TRAUMATIC BRAIN-INJURY; AMYLOID PRECURSOR PROTEIN; OXIDATIVE STRESS; D-GALACTOSE; TAU PHOSPHORYLATION; LIPID-PEROXIDATION; MITOCHONDRIAL DYSFUNCTION; COGNITIVE IMPAIRMENT; MEMORY IMPAIRMENT; IN-VITRO;
D O I
10.1002/med.21624
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Alzheimer's disease (AD), the most common form of dementia, is a progressive neurodegenerative disease. In the past decades, numbers of promising drug candidates showed significant anti-AD effects in preclinical studies but failed in clinical trials. One of the major reasons might be the limitation of appropriate animal models for evaluating anti-AD drugs. More than 95% of AD cases are sporadic AD (sAD). However, the anti-AD drug candidates were mainly tested in the familial AD (fAD) animal models. The diversity between the sAD and fAD might lead to a high failure rate during the development of anti-AD drugs. Therefore, an ideal sAD animal model is urgently needed for the development of anti-AD drugs. Here, we summarized the available sAD animal models, including their methodology, pathologic features, and potential underlying mechanisms. The limitations of these sAD animal models and future trends in the field were also discussed.
引用
收藏
页码:431 / 458
页数:28
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