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MERCURY 233<br />

Inorganic Mercury<br />

C<br />

2. HEALTH EFFECTS<br />

The acute- <strong>and</strong> intermediate-duration MRLs <strong>for</strong> oral exposure to inorganic mercury are based on kidney<br />

effects reported in a 1993 NTP study of mercuric chloride (NTP 1993). Most of the supporting studies of<br />

oral exposure to inorganic mercury also use mercuric chloride.<br />

Mercuric sulfide (also known as cinnabar) is the predominant natural <strong>for</strong>m of mercury in the environment<br />

<strong>and</strong> is a common ore from which metallic mercury is derived. Mercury released to the environment may be<br />

trans<strong>for</strong>med into mercuric sulfide. Several studies suggest that the bioavailability of mercuric sulfide in<br />

animals is less than that of mercuric chloride (Sin et al. 1983, 1990; Yeoh et al. 1986, 1989). For example,<br />

Sin et al. (1983) found an increase in tissue levels of mercury in mice orally exposed to low doses of<br />

mercuric chloride, but elevated levels of mercury were not found in the tissues of mice fed an equivalent<br />

weight of mercuric sulfide. This finding indicates a difference in bioavailability between HgCl2 <strong>and</strong> HgS in<br />

mice. However, a quantitative determination of the relative bioavailabilities of mercuric sulfide versus<br />

mercuric chloride has not been derived in the available studies, nor has the relative bioavailability of<br />

mercuric sulfide in humans been examined.<br />

An MRL of 0.007 mg Hg/kg/day has been derived <strong>for</strong> acute-duration oral exposure (14 days or<br />

less) to inorganic mercury.<br />

The MRL was based on a NOAEL of 0.93 mg Hg/kg/day <strong>for</strong> renal effects in rats administered mercuric<br />

chloride 5 days a week <strong>for</strong> 2 weeks. The dose used in this study was duration-adjusted <strong>for</strong> a 5-day/week<br />

exposure <strong>and</strong> divided by an uncertainty factor of 100 (10 <strong>for</strong> extrapolation from animals to humans <strong>and</strong><br />

10 <strong>for</strong> human variability). Increased absolute <strong>and</strong> relative kidney weights were observed in male rats<br />

exposed to 1.9 mg Hg/kg/day as mercuric chloride (NTP 1993). At higher doses, an increased incidence<br />

<strong>and</strong> severity of tubular necrosis was observed.<br />

Several other studies examining the effects of oral exposure to inorganic mercury salts have also shown<br />

renal toxicity in humans as a result of acute oral exposures. Kidney effects (i.e., heavy albuminuria,<br />

hypoalbuminemia, edema, <strong>and</strong> hypercholesterolemia) have been reported after therapeutic administration of<br />

inorganic mercury (Kazantzis et al. 1962). Acute renal failure has been observed in a number of case<br />

studies in which mercuric chloride had been ingested (Afonso <strong>and</strong> deAlvarez 1960; Murphy et al. 1979;<br />

Samuels et al. 1982). The autopsy of a 35-year-old man who ingested a lethal dose of mercuric chloride

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