| Literature DB >> 31328804 |
Lili Zhang1, Chen Chen1, Marvin Sh Mak2, Junfeng Lu1, Zeqing Wu1, Qiuhe Chen1, Yifan Han2,3,4, Yuefeng Li5, Rongbiao Pi1,3,6,7.
Abstract
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.Entities:
Keywords: animal model; mechanism; sporadic Alzheimer's disease
Mesh:
Year: 2019 PMID: 31328804 DOI: 10.1002/med.21624
Source DB: PubMed Journal: Med Res Rev ISSN: 0198-6325 Impact factor: 12.944