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. 2018 Aug 3;6(3):45.
doi: 10.3390/toxics6030045.

Health Impacts and Biomarkers of Prenatal Exposure to Methylmercury: Lessons from Minamata, Japan

Affiliations

Health Impacts and Biomarkers of Prenatal Exposure to Methylmercury: Lessons from Minamata, Japan

Mineshi Sakamoto et al. Toxics. .

Abstract

The main chemical forms of mercury are elemental mercury, inorganic divalent mercury, and methylmercury, which are metabolized in different ways and have differing toxic effects in humans. Among the various chemical forms of mercury, methylmercury is known to be particularly neurotoxic, and was identified as the cause of Minamata disease. It bioaccumulates in fish and shellfish via aquatic food webs, and fish and sea mammals at high trophic levels exhibit high mercury concentrations. Most human methylmercury exposure occurs through seafood consumption. Methylmercury easily penetrates the blood-brain barrier and so can affect the nervous system. Fetuses are known to be at particularly high risk of methylmercury exposure. In this review, we summarize the health effects and exposure assessment of methylmercury as follows: (1) methylmercury toxicity, (2) history and background of Minamata disease, (3) methylmercury pollution in the Minamata area according to analyses of preserved umbilical cords, (4) changes in the sex ratio in Minamata area, (5) neuropathology in fetuses, (6) kinetics of methylmercury in fetuses, (7) exposure assessment in fetuses.

Keywords: exposure assessment; fetus; kinetics; methylmercury; toxicity.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Individual methylmercury concentrations of preserved umbilical cords (μg/g dry weight) from the Minamata area and the amount of annual acetaldehyde production.
Figure 2
Figure 2
Comparisons of the distributions of lesions among adult and fetal-type cases of Minamata disease. Note: The distributions of degenerated neurons in adult (a) and fetal patients (b) are shown. (Modified from Reference [9] with permission).
Figure 3
Figure 3
Correlation coefficients (r) for the relationships among biomarkers of methylmercury exposure at parturition. Note: Red blood cells were used to calculate the correlations between the levels of methylmercury in blood, the placenta, and cord tissue (---) [30]. Whale blood was used to calculate the correlations between the methylmercury levels of blood, hair, and nails () [45].

References

    1. NRC (National Research Council) Toxicological Effects of Methylmercury. Academic Press; Washington, DC, USA: 2000.
    1. UNIDO (United Nations Industrial Development Organization) Protocols for Environmental and Health Assessment of Mercury Released by Artisanal and Small-Scale Gold Miners. United Nations Industrial Development Organization; Vienna, Austria: 2008.
    1. WHO (World Health Organization) Inorganic Mercury. Environmental Health Criteria 118. World Health Organization; Geneva, Switzerland: 1991.
    1. UNEP (United Nations Environment Programme) Global Mercury Assessment 2013: Sources, Emissions, Releases and Environmental Transport. UNEP Chemicals Branch; Geneva, Switzerland: 2013.
    1. WHO (World Health Organization) Methylmercury. Environmental Health Criteria 101. World Health Organization; Geneva, Switzerland: 1990.

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