Rapamycin and Alzheimer disease: a hypothesis for the effective use of rapamycin for treatment of neurodegenerative disease

被引:10
|
作者
Carosi, Julian M. [1 ]
Sargeant, Timothy J. [1 ]
机构
[1] South Australian Hlth & Med Res Inst SAHMRI, Hopwood Ctr Neurobiol, Lysosomal Hlth Ageing, Lifelong Hlth Theme, Adelaide, Australia
关键词
Alzheimer disease; autophagy; dementia; lysosome; rapamycin; AMYLOID-BETA; MOUSE MODEL; IMPROVES MEMORY; TRANSGENIC MICE; A-BETA; MTOR; DYSREGULATION; CLEARANCE; DEFICITS;
D O I
10.1080/15548627.2023.2175569
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In 2019 we summarized work relating to the potential use of rapamycin for treating Alzheimer disease (AD). We considered the commentary necessary because use of rapamycin in people with AD is a very real prospect and we wanted to present a balanced view of the likely consequences of MTOR (mechanistic target of rapamycin kinase) inhibition in the AD brain. We concluded that use of rapamycin, an MTOR inhibitor that increases macroautophagy/autophagy, could hold promise for prevention of AD if used early enough. However, MTOR inhibition appeared ineffectual in resolving existing amyloid pathology in AD mouse models. In this View article, we update these observations with new studies that have used rapamycin in AD models and provide evidence both for and against its use in AD. We also discuss rapamycin in the light of new research that describes rapamycin-induced autophagic stress in the aging brain and autophagic stress as the origin of the amyloid plaque itself. We conclude that rapamycin will have complex effects on the brain in AD. Further, we hypothesize that lysosomal degradative capacity in the brain will likely determine how effective or detrimental rapamycin will be as a treatment of AD.
引用
收藏
页码:2386 / 2390
页数:5
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