Mthfr deficiency and SARS‐CoV‐2 infection synergistically deplete dopamine and upregulate α‐synuclein increasing the risk of Parkinson's disease
Year: 2025
Type: article
Abstract: Background Methylene tetrahydrofolate reductase (MTHFR) is a critical enzyme in one‐carbon metabolism that affects several biological processes such as nucleotide synthesis, amino acid homeostasis, DNA methylation, redox defense, and neurotransmitter synthesis including dopamine. Common MTHFR polymorphisms increase the risk of vascular dementia and neurodegenerative diseases such as Parkinson's disease (PD) and are also associated with high COVID‐19 incidence and mortality. Furthermore, Mthfr‐deficient mice display cognitive deficits, cerebrovascular dysfunction, and a increased risk of PD‐like pathology. We hypothesized that SARS‐CoV‐2 infection could accelerate the onset or progression of vascular dementia and PD in the context of MTHFR deficiency as modeled by Mthfr heterozygous knockout ( Mthfr +/‐ ) mice. Methods We infected 10‐months‐old Mthfr +/‐ and wild type (WT) mice with mouse‐adapted (MA10) strain of SARS‐CoV‐2 (1 × 10 4 PFU) or with mock (PBS). Mice were monitored for weight loss and euthanized 3 days post‐infection (dpi). Brain and lung tissue were evaluated for viral titer, inflammation, blood‐brain‐barrier (BBB) permeability, and PD pathology. Untargeted metabolomics analysis was performed on plasma samples. Results Mthfr +/‐ and WT mice showed comparable weight loss and lung viral titer but no detectable virus in the brain following MA10 infection. Interestingly, we observed increased BBB disruption marked by reduced tight junction protein ZO‐1 and increased BBB leakage in Mthfr +/‐ MA10‐infected mice. MA10 infection also increased IL‐1β mRNA and microglia count in brains of Mthfr +/‐ mice. Metabolomics analysis showed significantly lower plasma dopamine in Mthfr +/‐ infected mice. In addition, MA10 infection significantly decreased tyrosine hydroxylase (TH) level and reduced TH+ dopaminergic neuron count, and increased α‐synuclein levels in substantia nigra of Mthfr +/‐ mice and reduced TH levels in the dorsal striatum. Conclusions SARS‐CoV‐2 infection leads to BBB dysfunction , neuroinflammation, and lower plasma dopamine levels in Mthfr +/‐ mice. It also decreases dopaminergic neurons in substantia nigra and dorsal striatum, while enhancing α‐synuclein levels in the substantia nigra. These effects may increase the risk of PD, particularly in the context of Mthfr deficiency.
Source: Alzheimer s & Dementia
Institution: Tulane University
Language: English
Subfield: Neurology
Field: Medicine
Domain: Health Sciences
Open Access status: hybrid
Estimated APC paid: $4,200
OpenAlex ID: W7117139387
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