# Neurotoxic Effect of Manganese and Vanadium Co-Exposure in Animal Models of Parkinson’s Disease

**Authors:** Alejandra Bargues-Carot, Naveen Kondru, Maddlyn Haller, Gary Zenitsky, Huajun Jin, Vellareddy Anantharam, Arthi Kanthasamy, Anumantha G. Kanthasamy

PMC · DOI: 10.3390/ijms27041757 · International Journal of Molecular Sciences · 2026-02-12

## TL;DR

Exposure to manganese and vanadium together worsens Parkinson's-like symptoms in mice with a genetic mutation linked to the disease.

## Contribution

This study reveals the neurotoxic effects of manganese and vanadium co-exposure in a Parkinson’s disease mouse model.

## Key findings

- Mn/V co-exposure caused significant brain accumulation and reduced locomotor activity in A53T mice.
- Olfactory deficits and anxiety-like behavior were observed in Mn/V-treated A53T mice but not in wild-type mice.
- Male A53T mice showed more pronounced neurotoxic effects from Mn/V co-exposure.

## Abstract

Chronic environmental exposure to mixtures of heavy metals like manganese (Mn) and vanadium (V) has been associated with Parkinson’s disease (PD). We investigated the poorly understood neurotoxic effects of Mn/V co-exposure on PD-relevant behavioral phenotypes in transgenic mice expressing the human alpha-synuclein (αSyn) A53T mutant. C57BL/6 wild-type (WT) and transgenic A53T mice were intranasally co-exposed to 100 µg MnCl2 and 75 µg V2O5 five times weekly for three months, simulating a 5-day workweek. This led to significant Mn/V accumulation in the brain. Exploratory locomotor activity declined significantly in Mn/V-treated A53T mice, but not in Mn/V-treated WT mice when compared to their respective vehicle controls. Motor coordination, assessed via a forced locomotor activity test, was not significantly affected in either group. In Mn/V-treated A53T mice, olfactory deficits were present, but not in Mn/V-treated WT mice. Behavioral despair, assessed by tail suspension and forced swim tests, was not induced by Mn/V co-exposure in any group compared to their vehicle controls. Mn/V-treated A53T mice exhibited anxiety-like behavior and hyperactivity. These findings suggest that Mn/V co-exposure exacerbates neurotoxic effects in A53T mice, with a more pronounced effect in males, providing insight into the role of metal mixture exposure in environmentally linked Parkinsonism.

## Linked entities

- **Chemicals:** manganese (PubChem CID 23930), vanadium (PubChem CID 23990), MnCl2 (PubChem CID 24480), V2O5 (PubChem CID 14814)
- **Diseases:** Parkinson’s disease (MONDO:0005180)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Snca (synuclein, alpha) [NCBI Gene 20617] {aka NACP, alpha-Syn, alphaSYN}, Prnp (prion protein) [NCBI Gene 19122] {aka CD230, PrP, PrP<C>, PrPC, PrPSc, Prn-i}
- **Diseases:** cognitive and motor deficits (MESH:D003072), motor dysfunction (MESH:D000068079), dislocation (MESH:D004204), rigidity (MESH:D009127), Parkinsonism (MESH:D010302), Lewy (MESH:D018827), degeneration of dopaminergic neurons (MESH:D009410), Depression (MESH:D003866), lethargy (MESH:D053609), weight loss (MESH:D015431), hyposmia (MESH:D000086582), impairments of vestibular coordination (MESH:D001259), Depressive Behavior (MESH:D011596), bradykinesia (MESH:D018476), tremors (MESH:D014202), postural instability (MESH:D054972), olfactory deficits (MESH:D000857), autonomic dysfunction (MESH:D001342), motor deficits (MESH:D009461), hyperactivity (MESH:D006948), learning and memory problems (MESH:D007859), neurobehavioral deficits (MESH:D019954), function (MESH:D003291), impaired locomotion (MESH:D020233), vestibular rolling (MESH:D015837), behavioral deficits (MESH:D019958), Anxiety (MESH:D001007), Lewy bodies (MESH:D020961), Neurotoxic (MESH:D020258), impaired (MESH:D060825), behavioral disease (MESH:D001523), sensory impairments (MESH:D012678), sleep disturbances (MESH:D012893), emotional disturbances (MESH:D014832), PD (MESH:D010300), Parkinsonian syndrome (MESH:D020734), neurodegeneration (MESH:D019636), injury to (MESH:D014947)
- **Chemicals:** nitric acid (MESH:D017942), Manganese (MESH:D008345), Y (MESH:D015019), arsenite (MESH:C015001), dopamine (MESH:D004298), lead (MESH:D007854), In (MESH:D007204), cadmium (MESH:D002104), hydrogen (MESH:D006859), ferrovanadium (MESH:C081363), CO2 (MESH:D002245), V2O5 (MESH:C066075), chromium (MESH:D002857), Bi (MESH:D001729), Chemicals and Reagents (-), Sc (MESH:D012538), hydrochloric acid (MESH:D006851), Cu (MESH:D003300), MnCl2 (MESH:C025340), isoflurane (MESH:D007530), Fe (MESH:D007501), V (MESH:D014639), Li (MESH:D008094), Tb (MESH:D013725), water (MESH:D014867), nickel (MESH:D009532), zinc (MESH:D015032), Metal (MESH:D008670)
- **Species:** Rodentia (rodent, order) [taxon 9989], Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116], Mus musculus (house mouse, species) [taxon 10090]
- **Mutations:** A53T
- **Cell lines:** C57BL/6 — Mus musculus (Mouse), Transformed cell line (CVCL_C0MU), /6 — Homo sapiens (Human), Tongue squamous cell carcinoma, Cancer cell line (CVCL_5985)

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12940837/full.md

## References

89 references — full list in the complete paper: https://tomesphere.com/paper/PMC12940837/full.md

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Source: https://tomesphere.com/paper/PMC12940837