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MERCURY 166<br />

2. HEALTH EFFECTS<br />

mercury excreted by the fecal route was significantly lower in the 500 compared to the 5 <strong>and</strong> 50 µM Hg<br />

group.<br />

The rate of oral absorption of mercuric mercury compounds in rats is dependent on several factors (e.g.,<br />

intestinal pH, compound dissociation) (Endo et al. 1990). Age <strong>and</strong> diet also can influence the extent of<br />

absorption in mice (Kostial et al. 1978). One-week-old suckling mice absorbed 38% of the orally<br />

administered mercuric chloride, whereas adult mice absorbed only 1% of the dose in st<strong>and</strong>ard diets. When<br />

the adult mice received a milk diet instead of the st<strong>and</strong>ard diet, absorption increased to 7% of the<br />

administered dose (Kostial et al. 1978).<br />

Several studies suggest that the bioavailability of mercuric sulfide in animals is less than that of mercuric<br />

chloride (Sin et al. 1983, 1990; Yeoh et al. 1986, 1989). For example, Sin et al. (1983) found an increase in<br />

tissue levels of mercury in mice orally exposed to low doses of mercuric chloride, but elevated levels of<br />

mercury were not found in the tissues of mice fed an equivalent weight of mercury as mercuric sulfide.<br />

This finding indicates a difference in bioavailability between HgCl2 <strong>and</strong> HgS in mice. However, a<br />

quantitative determination of the relative bioavailabilities of mercuric sulfide versus mercuric chloride has<br />

not been derived in the available studies. Furthermore, the relative bioavailability of mercuric sulfide in<br />

humans has not been examined.<br />

Organic Mercury. Organic mercury compounds are more readily absorbed by the oral route than inorganic<br />

mercury compounds. Based on retention <strong>and</strong> excretion studies in humans, approximately 95% of an oral<br />

tracer dose of aqueous methylmercuric nitrate was absorbed (Aberg et al. 1969). Absorption of mercury<br />

was also reported in studies in which volunteers received doses of methylmercury bound to protein<br />

(Miettinen 1973) or ate bread contaminated with a fungicide that contained methylmercury (Al-Shahristani<br />

et al. 1976); however, no quantitative data regarding the percentage of absorption were available.<br />

In vitro evidence suggests that organic mercury is also readily absorbed in the gastrointestinal tract <strong>and</strong> that<br />

methylmercuric chloride is absorbed to a greater extent than phenylmercuric chloride (Endo et al. 1989).<br />

Complexing of methylmercury with nonprotein sulfhydryls also may play a role in intestinal absorption <strong>and</strong><br />

reabsorption (Urano et al. 1990). Phenylmercuric salt in the diet was completely absorbed in mice<br />

(Clarkson 1972a) <strong>and</strong> readily absorbed in rats following long-term oral administration (Fitzhugh et al.<br />

1950). Absorption was nearly complete within 6 hours after female cynomolgus monkeys were given<br />

0.5 mg Hg/kg as methylmercuric chloride by gavage (Rice 1989b). Following a single oral exposure

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