Antimicrobial drugs for Parkinson's disease: Existing therapeutic strategies and novel drugs exploration

被引:0
作者
Fu, Mengjie [1 ]
Wang, Qiuchen [1 ]
Gao, Lihui [1 ]
Yuan, Xin [1 ]
Wang, Ju [1 ]
机构
[1] Tianjin Med Univ, Sch Biomed Engn, Tianjin 300070, Peoples R China
关键词
Parkinson's disease; Drug repurposing; Molecular docking; Molecular dynamics simulation; Antimicrobial drugs; ALPHA-SYNUCLEIN; RAT MODEL; PREVENTS; AGGREGATION; MINOCYCLINE; NEURODEGENERATION; NEUROPROTECTION; NEUROGENESIS; DOXYCYCLINE; DYSFUNCTION;
D O I
10.1016/j.arr.2024.102387
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Parkinson's disease (PD), the second most common neurodegenerative disorder, is characterized by loss of dopaminergic neurons in the substantia nigra, as well as the abnormal accumulation of misfolded alpha-synuclein. Clinically, PD is featured by typical motor symptoms and some non-motor symptoms. Up to now, although considerable progress has been made in understanding the pathogenesis of PD, there is still no effective therapeutic treatment for the disease. Thus, exploring new therapeutic strategies has been a topic that needs to be addressed urgently. Noteworthy, with the proposal of the microbiota-gut-brain axis theory, antimicrobial drugs have received significant attention due to their effects on regulating the intestinal microbiota. Nowadays, there is growing evidence showing that some antimicrobial drugs may be promising drugs for the treatment of PD. Data from pre-clinical and clinical studies have shown that some antimicrobial drugs may play neuroprotective roles in PD by modulating multiple biochemical and molecular pathways, including reducing alpha-synuclein aggregation, inhibiting neuroinflammation, regulating mitochondrial structure and function, as well as suppressing oxidative stress. In this paper, we summarized the effects of some antimicrobial drugs on PD treatment from recent preclinical and clinical studies. Then, we further discussed the potential of a few antimicrobial drugs for treating PD based on molecular docking and molecular dynamics simulation. Importantly, we highlighted the potential of clorobiocin as the therapeutic strategy for PD owing to its ability to inhibit alpha-synuclein aggregation. These results will help us to better understand the potential of antimicrobial drugs in treating PD and how antimicrobial drugs may alleviate or reverse the pathological symptoms of PD.
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页数:13
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