Targeting psychologic stress signaling pathways in Alzheimer's disease

被引:42
作者
Futch, Hunter S. [1 ,2 ,4 ]
Croft, Cara L. [1 ,2 ,4 ]
Truong, Van Q. [1 ,2 ,4 ]
Krause, Eric G. [3 ,4 ]
Golde, Todd E. [1 ,2 ,4 ]
机构
[1] Univ Florida, Dept Neurosci, Gainesville, FL 32610 USA
[2] Univ Florida, Ctr Translat Res Neurodegenerat Dis, Gainesville, FL 32610 USA
[3] Univ Florida, Dept Pharmacodynam, Coll Pharm, Gainesville, FL USA
[4] Univ Florida, McKnight Brain Inst, 1149 Newell Dr,POB 1000015, Gainesville, FL 32610 USA
关键词
Alzheimer's disease; Corticotropin-releasing hormone; Psychologic distress; Chronic stress; Neurodegeneration; CORTICOTROPIN-RELEASING-FACTOR; MILD COGNITIVE IMPAIRMENT; MESSENGER-RNA EXPRESSION; AMYLOID-BETA PRODUCTION; MOUSE MODEL; PARKINSONS-DISEASE; TRANSGENIC MICE; TAU PATHOLOGY; TG2576; MICE; RECEPTOR ANTAGONISTS;
D O I
10.1186/s13024-017-0190-z
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 prevalent progressive neurodegenerative disease; to date, no AD therapy has proven effective in delaying or preventing the disease course. In the search for novel therapeutic targets in AD, it has been shown that increased chronic psychologic stress is associated with AD risk. Subsequently, biologic pathways underlying psychologic stress have been identified and shown to be able to exacerbate AD relevant pathologies. In this review, we summarize the literature relevant to the association between psychologic stress and AD, focusing on studies investigating the effects of stress paradigms on transgenic mouse models of Amyloid-beta (A beta) and tau pathologies. In recent years, a substantial amount of research has been done investigating a key stress-response mediator, corticotropin-releasing hormone (CRH), and its interactions with AD relevant processes. We highlight attempts to target the CRH signaling pathway as a therapeutic intervention in these transgenic mouse models and discuss how targeting this pathway is a promising avenue for further investigation.
引用
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页数:10
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