# Neurobehavioral and Dopaminergic Dysfunctions Induced by Mixed Metal Exposure in C57BL/6 Mice

**Authors:** Daeun Lee, Haesoo Kim, Sarita Pyatha, Kisok Kim

PMC · DOI: 10.5812/ijpr-158559 · 2025-03-02

## TL;DR

Exposure to aluminum, lead, and mercury together harms mice brain function and reduces dopamine levels, leading to motor and behavioral issues.

## Contribution

This study is the first to investigate the combined effects of Al, Pb, and Hg on dopaminergic systems and neurobehavioral outcomes in mice.

## Key findings

- Mixed metal exposure reduced motor coordination and locomotor activity in mice.
- Dopamine levels in the striatum were significantly decreased after exposure.
- Key dopaminergic proteins like tyrosine hydroxylase and dopamine receptor D1 were downregulated.

## Abstract

Aluminum (Al), lead (Pb), and mercury (Hg) are major environmental pollutants, and a large population may be simultaneously exposed to these metals. However, studies on the potential neurobehavioral effects of mixed exposure to Al, Pb, and Hg are lacking.

This study aimed to evaluate neurobehavioral changes in mice following combined exposure to Al, Pb, and Hg and to investigate the effects of this exposure on dopaminergic neurotransmission within the striatum.

In this study, C57BL/6 mice (n = 10 per group) were assigned to control and metal-treated groups. Changes in motor coordination and locomotor activity that occurred when mice were simultaneously exposed to these metals via drinking water for 28 days were measured using the rotarod and open field tests. In addition, dopamine content and key factors involved in dopaminergic neurotransmission in the striatum were evaluated using real-time PCR and Western blot analysis.

The mixed metal exposure decreased motor function and significantly reduced the content of dopamine in the striatum of the experimental mice (P < 0.001). Expression of tyrosine hydroxylase, vesicular monoamine transporter 2, and dopamine receptor D1, which are involved in dopaminergic neurotransmission in the striatum, was significantly decreased (P < 0.01), whereas expression of the dopamine transporter was significantly increased (P < 0.05). Dopamine receptor D2 expression was not significantly changed by the mixed metal exposure.

These results suggest that mixed exposure to Al, Pb, and Hg inhibits normal dopaminergic neurotransmission, resulting in neurobehavioral disorders.

## Linked entities

- **Chemicals:** Aluminum (PubChem CID 123667), lead (PubChem CID 5352425), mercury (PubChem CID 23931)

## Full-text entities

- **Genes:** Slc18a2 (solute carrier family 18 (vesicular monoamine), member 2) [NCBI Gene 214084] {aka 1110037L13Rik, 9330105E13, Vmat2}, Th (tyrosine hydroxylase) [NCBI Gene 21823], Drd1 (dopamine receptor D1) [NCBI Gene 13488] {aka C030036C15Rik, Drd-1, Drd1a, Gpcr15}, Drd2 (dopamine receptor D2) [NCBI Gene 13489] {aka D2R, Drd-2}
- **Diseases:** neurobehavioral disorders (MESH:D019954), Dopaminergic Dysfunctions (MESH:D009422)
- **Chemicals:** dopamine (MESH:D004298), Pb (MESH:D007854), Hg (MESH:D008628), Al (MESH:D000535), Metal (MESH:D008670)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** C57BL/6 — Mus musculus (Mouse), Transformed cell line (CVCL_C0MU)

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12297027/full.md

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Source: https://tomesphere.com/paper/PMC12297027