Resveratrol targeting tau proteins, amyloid-beta aggregations, and their adverse effects: An updated review

被引:17
作者
Ashrafizadeh, Milad [1 ]
Zarrabi, Ali [2 ]
Najafi, Masoud [3 ]
Samarghandian, Saeed [4 ]
Mohammadinejad, Reza [5 ]
Ahn, Kwang Seok [6 ]
机构
[1] Univ Tabriz, Fac Vet Med, Dept Basic Sci, Tabriz, Iran
[2] Sabanci Univ, Nanotechnol Res & Applicat Ctr SUNUM, Tuzla, Turkey
[3] Kermanshah Univ Med Sci, Sch Paramed Sci, Radiol & Nucl Med Dept, Kermanshah, Iran
[4] Neyshabur Univ Med Sci, Dept Basic Med Sci, Neyshabur, Iran
[5] Kerman Univ Med Sci, Neurosci Res Ctr, Inst Neuropharmacol, Kerman 7619813159, Iran
[6] Kyung Hee Univ, Coll Korean Med, 47 Kyungheedae Gil, Seoul 130701, South Korea
基金
新加坡国家研究基金会;
关键词
aggregation; amyloid-beta; neurological disorders; neuroprotective; resveratrol; tau protein; ALZHEIMERS-DISEASE; A-BETA; BIOLOGICAL EVALUATION; SIGNALING PATHWAY; CANCER PREVENTION; OXIDATIVE STRESS; DIRECTED LIGANDS; MEDIATED NEURODEGENERATION; ENDOPLASMIC-RETICULUM; MULTITARGETED AGENTS;
D O I
10.1002/ptr.6732
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Resveratrol (Res) is a non-flavonoid compound with pharmacological actions such as antioxidant, antiinflammatory, hepatoprotective, antidiabetes, and antitumor. This plant-derived chemical has a long history usage in treatment of diseases. The excellent therapeutic impacts of Res and its capability in penetration into blood-brain barrier have made it an appropriate candidate in the treatment of neurological disorders (NDs). Tau protein aggregations and amyloid-beta (A beta) deposits are responsible for the induction of NDs. A variety of studies have elucidated the role of these aggregations in NDs and the underlying molecular pathways in their development. In the present review, based on the recently published articles, we describe that how Res administration could inhibit amyloidogenic pathway and stimulate processes such as autophagy to degrade A beta aggregations. Besides, we demonstrate that Res supplementation is beneficial in dephosphorylation of tau proteins and suppressing their aggregations. Then, we discuss molecular pathways and relate them to the treatment of NDs.
引用
收藏
页码:2867 / 2888
页数:22
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