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

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MERCURY 356<br />

2. HEALTH EFFECTS<br />

The mechanism of mercury toxicity is still largely unknown. It is not known whether there are unique<br />

mechanisms of action <strong>for</strong> the toxic effects in children that would require special consideration <strong>for</strong><br />

treatment modalities, but at present it appears that target site is determined more by the pharmacokinetics<br />

(i.e., which tissues end up with the highest levels) than by a specific mechanism of action (e.g., a receptor<br />

binding-process initiating type of mechanism).<br />

The results of a number of accidental food poisonings indicate that children are more vulnerable, <strong>and</strong> this<br />

vulnerability may be a function of easier access of mercury to the systemic circulation <strong>and</strong> brain, or it may<br />

be because disruption of cell growth <strong>and</strong> organization is more critical <strong>for</strong> children in developmental stages<br />

of growth. More data are needed to determine if the vulnerability of children is due to less plasticity to<br />

insult of analogous target tissue in adults, or because target tissues actually receive more toxic agent.<br />

There are not adequate biomarkers of exposure nor adequate access to biomarkers of exposure. Hair,<br />

urine, <strong>and</strong> blood levels are gross measures of body burden <strong>and</strong> do not provide the essential in<strong>for</strong>mation<br />

about levels of mercury at target tissues. Research is needed into better (preferably noninvasive)<br />

monitoring tools. Research is also needed on how to make monitoring tests readily <strong>and</strong> inexpensively<br />

available to the general public. Mercury is one of the top ten most hazardous substances, <strong>and</strong> its levels are<br />

increasing in the environment. There is considerable anxiety present in the general population about<br />

potential mercury toxicity from dental amalgam, but this occurs in the absence of good in<strong>for</strong>mation on<br />

actual body burdens. The general public <strong>and</strong> health officials would benefit from readily available ways <strong>for</strong><br />

individuals to measure personal <strong>and</strong> family member mercury body burdens.<br />

The interactions of immediate interest are those that either affect absorption from the gastrointestinal tract<br />

or that prevent or reduce mercury toxicity. No in<strong>for</strong>mation was identified to indicate that mercury<br />

interacts differently with iron or zinc, <strong>for</strong> example, in a child’s body then it would in an adult, although the<br />

difference in children’s physiology <strong>and</strong> morphology may result in a different response to that interaction.<br />

Except <strong>for</strong> the latter, which is again a toxicokinetic question, chemical interactions do not appear to be a<br />

data need.<br />

There is a data need to develop better chelation therapies, better ways to prevent absorption of mercury<br />

into the body of children, <strong>and</strong> better ways to interfere with the mechanism of action, especially <strong>for</strong> damage<br />

to the nervous system. The current literature continues to grow with case histories of poisonings where

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