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MERCURY 340<br />

2. HEALTH EFFECTS<br />

In<strong>for</strong>mation concerning metallic mercury exists primarily <strong>for</strong> the inhalation route of exposure in humans<br />

<strong>and</strong> animals (see Figure 2-8). Human data exist <strong>for</strong> all categories of effect following inhalation exposure<br />

to metallic mercury vapor. The results from inhalation studies in animals have been reported <strong>for</strong> all end<br />

points except immunological <strong>and</strong> genotoxic effects, <strong>and</strong> cancer. With the exception of case studies on<br />

contact dermatitis <strong>and</strong> neurological effects after acute <strong>and</strong> occupational dermal exposure to metallic<br />

mercury in humans, no studies were located <strong>for</strong> either the oral or dermal routes of exposure <strong>for</strong> either<br />

humans or animals.<br />

Existing in<strong>for</strong>mation on inorganic mercury salts is shown in Figure 2-9. No studies were found on the<br />

health effects from inhaled mercury salts in humans or animals. A number of case histories <strong>for</strong> acute or<br />

chronic oral exposure to mercury salts provide in<strong>for</strong>mation on systemic <strong>and</strong> neurological effects <strong>and</strong> death.<br />

Some case histories <strong>and</strong> occupational studies provide in<strong>for</strong>mation on dermal exposures to mercury salts at<br />

acute, intermediate, <strong>and</strong> chronic exposures leading to death, immunologic, neurologic, <strong>and</strong> systemic<br />

effects. No animal inhalation studies <strong>for</strong> inorganic mercury salts were identified, <strong>and</strong> only one acute study<br />

provides limited in<strong>for</strong>mation on death from dermal exposure. A number of animal studies that have<br />

investigated the effects from oral exposure to mercury salts provide good in<strong>for</strong>mation on systemic effects;<br />

limited in<strong>for</strong>mation on cancer, neurologic, immunologic, <strong>and</strong> genotoxic effects; <strong>and</strong> no in<strong>for</strong>mation on<br />

reproductive or developmental effects.<br />

In<strong>for</strong>mation on methylmercuric <strong>and</strong> phenylmercuric mercury is presented in Figures 2-10 <strong>and</strong> 2-11. These<br />

two <strong>for</strong>ms of organic mercury were chosen to represent the group of organic mercurials because they have<br />

been detected at Superfund sites, <strong>and</strong> because methylmercury is the predominant <strong>for</strong>m of organic mercury<br />

in the environment. There is a paucity of in<strong>for</strong>mation on phenylmercury. Only a few case histories are<br />

available <strong>for</strong> effects following inhalation exposure (death, acute or chronic systemic effects, <strong>and</strong><br />

neurologic effects), <strong>and</strong> the in<strong>for</strong>mation from these reports is very limited. Only one case history <strong>for</strong> acute<br />

systemic effects following dermal exposure to phenylmercury was identified. One chronic oral study in<br />

rats <strong>and</strong> a cancer study in rats <strong>and</strong> mice provide the only animal data <strong>for</strong> phenylmercury. In contrast, there<br />

are a number of human studies on systemic, neurologic, <strong>and</strong> developmental effects resulting from an oral<br />

exposure to methylmercury. No human toxicity data were identified <strong>for</strong> immunologic, reproductive, or<br />

genotoxic effect, nor <strong>for</strong> carcinogenicity. The human data <strong>for</strong> methylmercury are accompanied by a<br />

relatively large number of animal studies representing all three exposure durations <strong>and</strong> providing some,<br />

although often limited, in<strong>for</strong>mation <strong>for</strong> all health effects categories. As with phenylmercury, there are only<br />

a few case histories <strong>for</strong> inhalation <strong>and</strong> dermal exposures, with limited in<strong>for</strong>mation on neurologic <strong>and</strong>

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