Phenylpropanoids and Alzheimer's disease: A potential therapeutic platform

被引:29
|
作者
Kolaj, Igri [1 ,2 ]
Liyanage, S. Imindu [1 ]
Weaver, Donald F. [1 ,2 ,3 ]
机构
[1] Univ Hlth Network, Krembil Res Inst, Krembil Discovery Tower,60 Leonard Ave,4KD-473, Toronto, ON M5T 0S8, Canada
[2] Univ Toronto, Dept Chem, 80 St George St, Toronto, ON M5S 3H6, Canada
[3] Univ Toronto, Fac Med, 1 Kings Coll Circle, Toronto, ON M5S 1A8, Canada
关键词
Alzheimer's disease; Protein misfolding; Innate immune system; Mitochondrial dysfunction; Phenylpropanoids; AMYLOID PRECURSOR PROTEIN; NONSTEROIDAL ANTIINFLAMMATORY DRUGS; TEA EPIGALLOCATECHIN-3-GALLATE EGCG; INDUCED MICROGLIAL ACTIVATION; QUERCETIN INDUCES APOPTOSIS; BETA-INDUCED MITOCHONDRIAL; RESPONSE ELEMENT ACTIVITY; BLOOD-BRAIN-BARRIER; FACTOR-KAPPA-B; OXIDATIVE STRESS;
D O I
10.1016/j.neuint.2018.08.001
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 a neurodegenerative disorder, characterized by progressive dementia, neuroin-flammation and the accumulation of intracellular neurofibrillary tangles and extracellular plaques. The etiology of AD is unclear, but is generally attributed to four leading hypotheses: (i) abnormal folding and aggregation of amyloid-beta (A beta)/tau proteins (ii) activation of the innate immune system, (iii) mitochondrial dysfunction, and (iv) oxidative stress. To date, therapeutic strategies have largely focused on A beta-centric targets; however, the repeated failure of clinical trials and the continued lack of a disease-modifying therapy demand novel, multi-faceted approaches. Natural products are common molecular platforms in drug development; in AD, compounds from the plant phenylpropanoid metabolic pathway have yielded promising associations. Herein, we review developments in the pathogenesis of AD and the metabolism of phenylpropanoids in plants. We further discuss the role of these metabolites as relevant to the four leading mechanisms of AD pathogenesis, and observe multiple protective effects among phenylpropanoids against AD onset and progression.
引用
收藏
页码:99 / 111
页数:13
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