| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 2582978 | Environmental Toxicology and Pharmacology | 2015 | 9 Pages |
•Hfe deficiency alters brain distribution of iron and manganese.•Hfe deficiency restores manganese-induced impulsivity.•Hfe deficiency increases striatal dopamine D1 receptor expression.•Both Hfe deficiency and olfactory Mn exposure alter monoamine turnover in the striatum.
Manganese in excess promotes unstable emotional behavior. Our previous study showed that olfactory manganese uptake into the brain is altered in Hfe−/− mice, a model of iron overload hemochromatosis, suggesting that Hfe deficiency could modify the neurotoxicity of airborne manganese. We determined anxiety-related behavior and monoaminergic protein expression after repeated intranasal instillation of MnCl2 to Hfe−/− mice. Compared with manganese-instilled wild-type mice, Hfe−/− mice showed decreased manganese accumulation in the cerebellum. Hfe−/− mice also exhibited increased anxiety with decreased exploratory activity and elevated dopamine D1 receptor and norepinephrine transporter in the striatum. Moreover, Hfe deficiency attenuated manganese-associated impulsivity and modified the effect of manganese on the expression of tyrosine hydroxylase, vesicular monoamine transporter and serotonin transporter. Together, our data indicate that loss of HFE function alters manganese-associated emotional behavior and further suggest that HFE could be a potential molecular target to alleviate affective disorders induced by manganese inhalation.
