Metformin Prevents Dopaminergic Neuron Death in MPTP/P-Induced Mouse Model of Parkinson's Disease via Autophagy and Mitochondrial ROS Clearance

被引:192
|
作者
Lu, Ming [1 ]
Su, Cunjin [1 ]
Qiao, Chen [1 ]
Bian, Yaqi [1 ]
Ding, Jianhua [1 ]
Hu, Gang [1 ,2 ,3 ]
机构
[1] Nanjing Med Univ, Dept Pharmacol, Jiangsu Key Lab Neurodegenerat, 140 Hanzhong Rd, Nanjing 210029, Jiangsu, Peoples R China
[2] Nanjing Normal Univ, Biomed Funct Mat Collaborat Innovat Ctr, Coll Chem & Mat Sci, Nanjing, Jiangsu, Peoples R China
[3] Nanjing Univ Chinese Med, Dept Pharmacol, Nanjing, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
AMPK; autophagy; metformin; mitochondrial ROS; Parkinson's disease; ACTIVATED PROTEIN-KINASE; HIGH-FAT DIET; NEURODEGENERATIVE DISEASES; METABOLIC INFLAMMATION; BRAIN INFLAMMATION; ALZHEIMERS-DISEASE; MICE; CANCER; ENERGY; CELLS;
D O I
10.1093/ijnp/pyw047
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Our previous study demonstrated that metabolic inflammation exacerbates dopaminergic neuronal degeneration in type 2 diabetes mice. Metformin, a typical oral hypoglycemic agent for diabetes, has been regarded as an activator of AMP-activated protein kinase and a regulator of systemic energy metabolism. Although metformin plays potential protective effects in many disorders, it is unclear whether metformin has a therapeutic role in dopaminergic neuron degeneration in Parkinson's disease. In the present study, a 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine plus probenecid-induced mouse model of Parkinson's disease was established to explore the neuroprotective effect of metformin on dopaminergic neurons in substania nigra compacta. We next cultured SH-SY5Y cells to investigate the mechanisms for the neuroprotective effect of metformin. We showed that treatment with metformin (5mg/mL in drinking water) for 5 weeks significantly ameliorated the degeneration of substania nigra compacta dopaminergic neurons, increased striatal dopaminergic levels, and improved motor impairment induced by 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine plus probenecid. We further found that metformin inhibited microglia overactivation-induced neuroinflammation in substania nigra compacta of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine plus probenecid Parkinson's disease mice, which might contribute to the protective effect of metformin on neurodegeneration. Furthermore, metformin (2mM) activated AMP-activated protein kinase in SH-SY5Y cells, in turn inducing microtubule-associated protein 1 light chain 3-II-mediated autophagy and eliminating mitochondrial reactive oxygen species. Consequently, metformin alleviated MPP+-induced cytotoxicity and attenuated neuronal apoptosis. Our findings demonstrate that metformin may be a pluripotent and promising drug for dopaminergic neuron degeneration, which will give us insight into the potential of metformin in terms of opening up novel therapeutic avenues for Parkinson's disease.
引用
收藏
页码:1 / 11
页数:11
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