| dc.description.abstract | Methylmercury (MeHg), a known neurotoxicant, is found in seafood, leading to regular exposure of humans to this compound. Many of the molecular targets and detoxifying components of MeHg toxicity, including glutathione (GSH), metallothioneins (MTs), and heat shock proteins (HSPs) have been identified; however, the molecular mechanisms of MeHg neurotoxicity are largely unknown. We used the model organism, Caenorhabditis elegans, to elucidate some of these mechanisms. We found that, although MeHg accumulated within C. elegans and caused a delay in development and a decrease in pharyngeal pumping rate, many endpoints, including life span, brood size, thrashing rate, and, most surprisingly, nervous system morphology, were unaffected. This finding led to the hypothesis that C. elegans has unique mechanisms for protecting its nervous system from MeHg neurotoxicity. We examined the involvement of GSH, MTs, and HSPs in MeHg toxicity in C. elegans and found that GSH levels were altered upon MeHg exposure, a glutathione s-transferase was highly upregulated upon exposure, and that the lack of MTs in MT knockout animals resulted in increased sensitivity to this toxicant. We also demonstrated that MeHg can induce hormesis in C. elegans, likely at least partially due to the involvement of GSTs in MeHg toxicity. As a result of our findings, we began to elucidate some of the molecular mechanisms of MeHg neuroprotection in the C. elegans model system. Our findings are highly valuable to the field of human health due to the regular exposure of humans to MeHg. | |
