Peripheral clearance of brain-derived Aβ in Alzheimer's disease: pathophysiology and therapeutic perspectives

被引:117
|
作者
Cheng, Yuan [1 ,2 ,3 ,4 ]
Tian, Ding-Yuan [1 ,2 ,3 ,4 ]
Wang, Yan-Jiang [1 ,2 ,3 ,4 ,5 ]
机构
[1] Third Mil Med Univ, Daping Hosp, Dept Neurol, Chongqing, Peoples R China
[2] Third Mil Med Univ, Daping Hosp, Ctr Clin Neurosci, Chongqing, Peoples R China
[3] Third Mil Med Univ, Inst Brain & Intelligence, Chongqing, Peoples R China
[4] Key Lab Aging & Brain Dis, Chongqing, Peoples R China
[5] Chinese Acad Sci, Ctr Excellence Brain Sci & Intelligence Technol, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
Alzheimer's disease; Beta-amyloid (A beta); Blood-brain barrier; Lymphatic vessel; Venous sinus; Periphery; Liver; Kidney; Intestine; Skin; Blood; Monocyte; Enzymes; RECEPTOR-RELATED PROTEIN-1; AMYLOID PRECURSOR PROTEIN; CEREBROSPINAL-FLUID ABSORPTION; INSULIN-DEGRADING ENZYME; TRANSGENIC MOUSE MODEL; CHRONIC KIDNEY-DISEASE; BLOOD-BRAIN; DENSITY-LIPOPROTEIN; APOLIPOPROTEIN-E; COMPLEMENT INTERACTIONS;
D O I
10.1186/s40035-020-00195-1
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Alzheimer's disease (AD) is the most common type of dementia, and no disease-modifying treatments are available to halt or slow its progression. Amyloid-beta (A beta) is suggested to play a pivotal role in the pathogenesis of AD, and clearance of A beta from the brain becomes a main therapeutic strategy for AD. Recent studies found that A beta clearance in the periphery contributes substantially to reducing A beta accumulation in the brain. Therefore, understanding the mechanism of how A beta is cleared in the periphery is important for the development of effective therapies for AD. In this review, we summarized recent findings on the mechanisms of A beta efflux from the brain to the periphery and discuss where and how the brain-derived A beta is cleared in the periphery. Based on these findings, we propose future strategies to enhance peripheral A beta clearance for the prevention and treatment of AD. This review provides a novel perspective to understand the pathogenesis of AD and develop interventions for this disease from a systemic approach.
引用
收藏
页数:11
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