Metformin Prevents Dopaminergic Neuron Death in MPTP/P-Induced Mouse Model of Parkinson's Disease Via Autophagy and Mitochondrial ROS Clearance
Overview
Affiliations
Background: 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.
Methods: 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.
Results: 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.
Conclusions: 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.
Neurotoxic Effects of Atrazine on Dopaminergic System via miRNAs and Energy-Sensing Pathways.
Chen X, Hu X, Liu H, He J, Li Y, Zhang X Mol Neurobiol. 2025; .
PMID: 40085354 DOI: 10.1007/s12035-025-04822-8.
Metformin and Cognitive Performance in Patients With Type 2 Diabetes: An Umbrella Review.
Enderami A, Shariati B, Zarghami M, Aliasgharian A, Ghazaiean M, Darvishi-Khezri H Neuropsychopharmacol Rep. 2025; 45(1):e12528.
PMID: 39871536 PMC: 11772738. DOI: 10.1002/npr2.12528.
Mitochondria and the Repurposing of Diabetes Drugs for Off-Label Health Benefits.
Yip J, Chiang G, Lee I, Lehming-Teo R, Dai K, Dongol L Int J Mol Sci. 2025; 26(1.
PMID: 39796218 PMC: 11719901. DOI: 10.3390/ijms26010364.
Hashmi M, Fatima H, Ahmad S, Rehman A, Safdar F Ibrain. 2024; 10(4):395-426.
PMID: 39691424 PMC: 11649393. DOI: 10.1002/ibra.12183.
Glucose Metabolism Disorders and Parkinson's Disease: Coincidence or Indicator of Dysautonomia?.
Chmiela T, Jarosz-Chobot P, Gorzkowska A Healthcare (Basel). 2024; 12(23).
PMID: 39685083 PMC: 11641510. DOI: 10.3390/healthcare12232462.