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| Teratology 1987 Dec;36(3):321-8 |
Related Articles,
|
Mercury 203 distribution
in pregnant and nonpregnant rats following
systemic infusions with thiol-containing
amino acids.
Aschner M, Clarkson TW.
Environmental Health Sciences Center,
School of Medicine and Dentistry,
University of Rochester, New York 14642.
Near-term pregnant (gestational day 17) and
nonpregnant Long-Evans female rats were
continuously infused into the external
jugular vein with 0.1 mmole/hour L-cysteine,
0.1 mmole/hour L-leucine, or saline. At 24,
48, and 72 hours, 50 mumole/hour
[203Hg]-MeHgCl was administered over 1
hour.
Total 203Hg body burden, brain, kidney, liver, and blood 203Hg concentrations were determined at 96 hours by gamma scintillation spectrometry. Despite significantly greater 203Hg whole body retention in the pregnant animals 203Hg concentrations in blood, brain, kidney, and liver were higher in nonpregnant rats.
In addition, brain 203Hg concentrations in both pregnant and virgin rats were significantly higher in L-cysteine-treated rats compared with controls.
These results suggest that the fetus may act as a "sink" for MeHg, thus decreasing 203Hg concentrations in maternal blood, brain, kidney, and liver.
Furthermore, the data indicate that brain
uptake of methylmercury in both pregnant
and nonpregnant rats is enhanced by chronic
L-cysteine infusion, lending support to the
hypothesis that methylmercury in the rat
may be translocated across the blood-brain
barrier by the neutral amino acid carrier
transport system.
PMID: 3424221 [PubMed - indexed for
MEDLINE]
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