A Toxological Analysis of Mercury


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Distribution / Excretion

Methylmercury Distribution

Methylmercury enters the body through different routes of exposure and is able to easily cross membrane barriers including the blood-brain barrier because organic mercury is transported into tissues by a methylmercury-cysteine complex. The methylmercuric cation has high affinity for this particular amino acid because it contains sulfhydryl groups. The metabolism of organic mercury occurs at a slow rate, which allows time for the methylmercury to enter the membrane barriers. So as the methylmercury complexes enter the membrane barriers, they begin to metabolize into inorganic mercury. This results in a great degree of ionic mercury accumulation in tissues including brain tissues. The half-life of methylmercury in the blood and brain are very different due to this accumulation in brain tissue. Blood half-life for humans is 49-164 days and the half-life for brain may be significantly longer. In addition to the accumulation of mercury in the brain and other body tissues, mercury has also been found to accumulate in fetal umbilical cords.


Methylmercury Excretion

 

The overall half-life of methylmercury in the body is 70-80 days. Reabsorption of methylmercury occurs within the bile which results in this long half-life as indicated above. Secretion occurs through a complexation between methylmercury and glutathione, which then enters the bile via a glutathione carrier protein. This complex may be reabsorbed by the gall bladder or intestines and re-enter the bloodstream once again. However, at some point, microorganisms in the intestinal tract may break down the methylmercury into the inorganic counterpart. This allows methylmercury to finally become fecally excreted as mercuric mercury. Most excretion occurs through the feces, however, as time increases urinary excretion slightly increases as well (after approximately 100 days urinary excretion is roughly 20%). Another form of unfortunate excretion is through lactation. The clearance of methylmercury from blood occurs faster for lactating mothers than those who are not lactating, most likely due to increased food intake, biliary action and changing levels of hormones. This results in a higher concentration of mercury in breast milk. “The ratio of mercury in breast milk to mercury in whole blood was approximately 1:20 in women exposed to methylmercury via contaminated grain in Iraq between 1971 and 1972. Evidence from the Iraqi poisoning incident also showed that lactation decreased blood mercury clearance half-times from 75 days in males and nonlactating females to 42 days in lactating females; the faster clearance due to lactation was confirmed in mice.”

 

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