1999
DOI: 10.1006/enrs.1998.3889
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In UteroMethylmercury Exposure Differentially Affects the Activities of Selenoenzymes in the Fetal Mouse Brain

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Cited by 116 publications
(66 citation statements)
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“…Whether this accumulation of MeHg in placenta causes any adverse effects in humans is not known. Studies on mice have shown effects on the activity of selenoenzymes, such as inhibition of glutathione peroxidase, although the placental concentration of selenium was not affected (33). Glutathione peroxidase is an antioxidative enzyme, and high levels are probably needed in the placenta to protect the fetus from the oxidative stress produced during the metabolism of MeHg (34).…”
Section: Discussionmentioning
confidence: 99%
“…Whether this accumulation of MeHg in placenta causes any adverse effects in humans is not known. Studies on mice have shown effects on the activity of selenoenzymes, such as inhibition of glutathione peroxidase, although the placental concentration of selenium was not affected (33). Glutathione peroxidase is an antioxidative enzyme, and high levels are probably needed in the placenta to protect the fetus from the oxidative stress produced during the metabolism of MeHg (34).…”
Section: Discussionmentioning
confidence: 99%
“…Dietary selenium is postulated to protect against mercury toxicity and the mercury-dependent inhibition of selenoenzyme activity. Additional dietary selenium has been shown to offset the selenium sequestered by mercury and thereby maintain normal antioxidant activity of brain selenoenzymes [39][40][41][42][43][44] . Increasing blood Hg:Se ratios are indicative of increasing risk or harm, therefore, assessment of MeHg exposure should involve the evaluation of blood Hg:Se ratios, rather than mercury levels alone.…”
Section: Biological Functions Of Selenoneine In Fishmentioning
confidence: 99%
“…Therefore, intracellular methylmercury tends to diminish the amount of selenium that is biologically available for normal selenoenzyme synthesis, especially as Hg:Se molar ratios approach or exceed a 1:1 stoichiometry. Protective effects of dietary selenium against mercury toxicity (Ganther et al, 1972;Prohaska and Ganther, 1977;Watanabe et al, 1999a,b;Ralston et al, 2007;Yang et al, 2008), and in prevention of mercury-dependent inhibition of selenoenzyme activities (Prohaska and Ganther, 1977;Watanabe et al, 1999b), appear to occur because additional dietary selenium is able to offset the selenium sequestered by mercury and thereby maintain normal antioxidant activities of brain selenoenzymes.…”
Section: Introductionmentioning
confidence: 99%