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revised final - Agency for Toxic Substances and Disease Registry ...

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MERCURY 185<br />

2.3.4 Elimination <strong>and</strong> Excretion<br />

2. HEALTH EFFECTS<br />

Elimination of metallic mercury occurs through the urine, feces, <strong>and</strong> expired air, while inorganic mercury is<br />

excreted in the urine <strong>and</strong> feces in humans. Animal data on excretion are limited but indicate that excretion<br />

is species <strong>and</strong> dose dependent. The feces are a major elimination route <strong>for</strong> inorganic mercury compounds,<br />

but high acute doses increase the percentage of excretion via the urine. Excretion of organic mercury is<br />

predominantly thought to occur through the fecal (biliary) route in humans. In animals, phenylmercury is<br />

excreted initially though the bile <strong>and</strong> then shifts to urine, whereas methylmercury is primarily excreted in<br />

the bile <strong>and</strong> then the feces. Age is a factor in the elimination of mercury in rats following inorganic <strong>and</strong><br />

organic mercury exposure, with younger rats demonstrating significantly higher retention than older rats.<br />

Both inorganic <strong>and</strong> organic mercury compounds can be excreted in breast milk. There are no data<br />

suggesting that the route of exposure affects the ultimate elimination of inorganic <strong>and</strong> organic mercury that<br />

is absorbed into the body.<br />

Metallic <strong>and</strong> Inorganic Mercury. The urine <strong>and</strong> feces are the main excretory pathways of metallic <strong>and</strong><br />

inorganic mercury in humans, with a body burden half-life of approximately 1–2 months (Clarkson 1989).<br />

In a study of <strong>for</strong>mer chloralkali workers exposed to metallic mercury vapor <strong>for</strong> 2–18 years (median,<br />

5 years), Sallsten et al. (1995) found that the elimination of mercury in urine was well characterized by a<br />

one-compartment model, which estimated a half-life of 55 days. There was a tendency toward longer half-<br />

lives with shorter duration exposures than with long-term exposure, when uptake <strong>and</strong> elimination have<br />

reached a steady state. This might be due to the induction of a higher metabolic rate after a longer exposure<br />

time, but there is no experimental evidence to support such an effect (Sallsten et al. 1995). For high-level<br />

exposure to inorganic divalent mercury, the urine is probably the major elimination route, with a half-life<br />

similar to that of metallic mercury (Clarkson 1989). An elimination half-life from urine was estimated to be<br />

25.9 days following an acute exposure to a high level of mercuric chloride (13.8 mg/kg) (Suzuki et al.<br />

1992). Exhalation in the lungs <strong>and</strong> secretion in saliva, bile, <strong>and</strong> sweat may also contribute a small portion<br />

to the excretion process (Joselow et al. 1968b; Lovejoy et al. 1974). After an acute mercury exposure in<br />

humans, urinary excretion accounts <strong>for</strong> 13% of the total body burden. After long-term exposure, urinary<br />

excretion increases to 58%. Humans inhaling mercury vapor <strong>for</strong> less than an hour expired approximately<br />

7% of the retained dose of mercury (Cherian et al. 1978; Hursh et al. 1976). The half-life <strong>for</strong> this<br />

elimination pathway was 14–25 hours; there<strong>for</strong>e, excretion through expired air is negligible 5–7 days after<br />

exposure (Cherian et al. 1978). Using a two-compartment model, elimination half-lives in the urine of<br />

workers exposed <strong>for</strong> 20–45 hours to >0.1 mg/m 3 metallic mercury vapor were

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