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MERCURY 178<br />

2. HEALTH EFFECTS<br />

This finding supports the assumption by Suda et al. (1989) that ingested methylmercury is dealkylated to<br />

inorganic mercury in the brain.<br />

Monkeys were fed 0.05 or 0.09 mg Hg/kg/day as methylmercury, containing 5% impurity of inorganic<br />

mercury, <strong>for</strong> 0.5–1.5 years (Lind et al. 1988). The low-dosed monkeys were found to have 10–33% of the<br />

total mercury present in the inorganic <strong>for</strong>m in brain cortices, while the high-dosed monkeys had 90% in the<br />

inorganic <strong>for</strong>m. Demethylation of methylmercury in the brain, as well as in other organs, including the<br />

kidneys <strong>and</strong> liver, is believed to contribute substantially to the high concentration of inorganic mercury in<br />

the brain. Following oral exposure to methylmercuric chloride, regional distribution of total mercury in<br />

the brain of monkeys was observed; the highest levels were in the thalamus <strong>and</strong> hypothalamus (Rice<br />

1989b).<br />

In contrast, in the brain of 21-day-old neonatal rats that had been previously exposed to a gavage dose of<br />

6.4 mg Hg/kg as methylmercury chloride in utero, the cerebellum had the highest mercury concentrations<br />

<strong>and</strong> the brainstem had the lowest (Braghiroli et al. 1990). By 60 days of age, concentrations in the brain<br />

reached normal values, with an estimated half-life of approximately 37 days (Braghiroli et al. 1990).<br />

There<strong>for</strong>e, age can affect regional distribution in the brain of animals.<br />

Massie et al. (1993) reported no significant change in the total amount of mercury in the organs (lung,<br />

heart, kidney, brain, <strong>and</strong> liver) of male C57BL/6J mice ranging in age from 133 to 904 days of age<br />

maintained under conventional conditions with no known source of mercury exposure other than<br />

background concentrations. The ratio of mercury in the brain to that in the liver or to that in the kidney<br />

was significantly increased with age, indicating that older mice are less able to maintain a low brain-toliver<br />

ratio of mercury regardless of the total body content of mercury.<br />

In a study of organs from sledge dogs fed methylmercury-laden meat <strong>and</strong> organs from predatory marine<br />

animals (Hansen <strong>and</strong> Danscher 1995), the highest concentration of total mercury was found in the<br />

mesenterial lymph nodes, followed by liver <strong>and</strong> kidneys, indicating that the lymphatic system may play an<br />

important role in the transport of mercury to target organs. The tissue concentrations of mercury observed<br />

in this study were found to be age-related, <strong>and</strong> the results suggest that demethylation takes place in all<br />

organs, except the skeletal muscle. Demethylation of methylmercury was found to be lower in the brain<br />

than in other organs (Hansen <strong>and</strong> Danscher 1995).<br />

Mercury accumulates in hair following exposure to methylmercury in humans <strong>and</strong> mice (Gr<strong>and</strong>jean et al.

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