Neuroprotective Natural Products for the Treatment of Parkinson's Disease by Targeting the Autophagy-Lysosome Pathway: A Systematic Review

被引:41
|
作者
Wang, Zi-Ying [1 ,2 ]
Liu, Jing-Yi [1 ,2 ]
Yang, Chuan-Bin [1 ,2 ]
Malampati, Sandeep [1 ,2 ]
Huang, Ying-Yu [1 ,2 ]
Li, Mei-Xiang [1 ,2 ]
Li, Min [1 ]
Song, Ju-Xian [1 ]
机构
[1] Hong Kong Baptist Univ, Sch Chinese Med, Kowloon, Hong Kong, Peoples R China
[2] Hong Kong Baptist Univ, Mr & Mrs Ko Chi Ming Ctr Parkinsons Dis Res, Kowloon, Hong Kong, Peoples R China
关键词
Parkinson's disease; autophagy; neuroprotection; natural products; UBIQUITIN-PROTEASOME SYSTEM; ALPHA-SYNUCLEIN; RAT MODEL; NEURODEGENERATIVE DISEASES; OXIDATIVE STRESS; CELLULAR-MODELS; DOWN-REGULATION; SH-SY5Y CELLS; MTOR; DEGRADATION;
D O I
10.1002/ptr.5834
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The autophagy-lysosome pathway (ALP) is a primary means by which damaged organelles and long-lived proteins are removed from cells and their components recycled. Impairment of the ALP has been found to be linked to the pathogenesis of Parkinson's disease (PD), a chronic neurodegenerative disorder characterized by the accumulation of protein aggregates and loss of dopaminergic neurons in the midbrain. In recent years, some active compounds derived from plants have been found to regulate the ALP and to exert neuroprotective effects in experimental models of PD, raising the possibility that autophagy enhancement may be an effective therapeutic strategy in PD treatment. In this review, we summarize recent findings of natural products that enhance ALP and thereby protect against PD. Research articles were retrieved from PubMed using relevant keywords in combination. Papers related to the topic were identified, and then the reliability of the experiments was assessed in terms of methodology. The results suggest that targeting the ALP with natural products is a promising strategy for PD treatment. However, risk of bias exists in some studies due to the defective methodology. Rigorous experimental design following the guidelines of autophagy assays, molecular target identification and in vivo efficacy evaluation is critical for the development of ALP enhancers for PD treatment in future studies. Copyright (C) 2017 John Wiley & Sons, Ltd.
引用
收藏
页码:1119 / 1127
页数:9
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