Journal
NEUROSCIENCE LETTERS
Volume 504, Issue 1, Pages 40-44Publisher
ELSEVIER IRELAND LTD
DOI: 10.1016/j.neulet.2011.08.053
Keywords
Heavy metals; Environmental toxins; Voles; Cytokines; Chemokines; Autism
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Funding
- OSU-CHS
- NIH [NS062664, HD48462]
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Mercury is neurotoxic and increasing evidence suggests that environmental exposure to mercury may contribute to neuropathologies including Alzheimer's disease and autism spectrum disorders. Mercury is known to disrupt immunocompetence in the periphery, however, little is known about the effects of mercury on neuroimmune signaling. Mercury-induced effects on central immune function are potentially very important given that mercury exposure and neuroinflammation both are implicated in certain neuropathologies (i.e., autism). Furthermore, mounting evidence points to the involvement of glial activation in autism. Therefore, we utilized an in vivo model to assess the effects of mercury exposure on neuroimmune signaling. In prairie voles, 10 week mercury exposure (60 ppm HgCl2 in drinking water) resulted in a male-specific increase in TNF alpha protein expression in the cerebellum and hippocampus. These findings are consistent with our previously reported male-specific mercury-induced deficits in social behavior and further support a role for heavy metals exposure in neuropathologies such as autism. Subsequent studies should further evaluate the mechanism of action and biological consequences of heavy metals exposure. Additionally, these observations highlight the potential of neuroimmune markers in male voles as biomarkers of environmental mercury toxicity. (C) 2011 Elsevier Ireland Ltd. All rights reserved.
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