Progress on Aβ-Targeted Therapeutic Strategies for Alzheimer's Disease

被引:6
作者
Hua Qian [1 ]
Ding Hai-Min [1 ]
Liang Mi [1 ]
机构
[1] Beijing Univ Chinese Med, Sch Preclin Med, Beijing 100029, Peoples R China
基金
中国国家自然科学基金;
关键词
Alzheimer's disease; beta-amyloid peptides; immunotherapy; presymptomatical treatment; AMYLOID PRECURSOR PROTEIN; GAMMA-SECRETASE INHIBITORS; PHASE-II; IMMUNOTHERAPY; PATHOLOGY; BRAIN; IMMUNIZATION; TOXICITY; CLEAVAGE; GROWTH;
D O I
10.3724/SP.J.1206.2012.00215
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Alzheimer's disease (AD) is the most common cause of dementia among the elderly people. The prevailing hypothesis for the pathological progression of AD is the beta-amyloid peptide (A beta) cascade hypothesis: oligomeric forms of A beta with cytotoxicity are the main cause of neuronal death in the brain of the AD patients. Thus, the inhibition of A beta production and aggregation as well as improvement of its clearance appear to be the main strategy for drug development. However, the disturbing issue is that no significantly effective approach is available yet although a large number of compounds have been trialed on clinic. It questions the hypothesis that A beta is the key pathologic factor leading to AD progression. The other possibility of failure is that loss of neural cells is so extensive that any treatment becomes not available when cognitive symptoms are apparent. New diagnostic ways may help to identify individuals before substantial neural damage has occurred. Treatments could then be attempted to stave off the onset of the disorders or the progression of the disease.
引用
收藏
页码:734 / 740
页数:7
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