Vahter M E, Mottet N K, Friberg L T, Lind S B, Charleston J S, Burbacher T M
Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden.
Toxicol Appl Pharmacol. 1995 Oct;134(2):273-84. doi: 10.1006/taap.1995.1193.
Total (T-Hg) and inorganic (I-Hg) mercury concentrations were determined in specific brain sites (cerebellum, occipital pole, pons, motor strip, frontal pole, temporal pole, thalamus, and pituitary) of female Macaca fascicularis monkeys exposed to daily peroral doses (50 micrograms Hg/kg body weight) of methyl mercury (MeHg) for 6, 12, or 18 months, or to continuous iv infusion of HgCl2 (200 micrograms Hg/kg body wt). In normal weight monkeys (2.4-4.1 kg body wt), the average concentration of MeHg (calculated as T-Hg minus I-Hg) was about the same in all brain sites, except the pituitary--3.0 micrograms Hg/g at 6 months, 4.2 micrograms/g at 12 months, and 4.3 micrograms Hg/g at 18 months. MeHg concentrations in the pituitary were about 50% of those in the other brain sites. In a group of monkeys that were kept unexposed for 6 months following 12 months of MeHg exposure, T 1/2 for MeHg was about 37 days in all brain sites, with the exception of the pituitary, where it was shorter. The concentration of I-Hg increased in all brain sites, but especially in the thalamus and pituitary, with the time of MeHg exposure. In most brain sites, I-Hg constituted about 9% of T-Hg at 6 and 12 months, and 12% of T-Hg at 18 months. In the pituitary, I-Hg increased from 20% of T-Hg at 6 months to 46% at 18 months. Elimination T 1/2 for I-Hg was extremely long, 230-540 days in most brain sites and considerably longer in the thalamus and pituitary. The concentration of I-Hg in the thalamus did not decrease during the clearance period (6 months), while I-Hg in the pituitary continued to increase in spite of no additional exposure. The MeHg exposed monkeys had several times higher I-Hg concentrations in the brain than monkeys exposed to HgCl2, indicating that I-Hg was formed by demethylation of MeHg in the brain, and not by brain uptake of I-Hg formed by demethylation elsewhere in the body. There were large variations in the relative concentration of I-Hg between individual monkeys, but not between brain sites (except thalamus and pituitary). Obese monkeys (5.0-6.1 kg body wt) exposed to MeHg had higher concentrations of both MeHg and I-Hg than normal weight monkeys in all brain sites, except in the pituitary.
测定了每日经口给予甲基汞(MeHg)(50微克汞/千克体重)6、12或18个月,或持续静脉输注氯化汞(HgCl2)(200微克汞/千克体重)的雌性食蟹猴特定脑区(小脑、枕极、脑桥、运动区、额极、颞极、丘脑和垂体)中的总汞(T-Hg)和无机汞(I-Hg)浓度。在正常体重的猴子(体重2.4 - 4.1千克)中,除垂体外,所有脑区中MeHg的平均浓度(计算为T-Hg减去I-Hg)大致相同——6个月时为3.0微克汞/克,12个月时为4.2微克/克,18个月时为4.3微克汞/克。垂体中的MeHg浓度约为其他脑区的50%。在一组经12个月MeHg暴露后又6个月未暴露的猴子中,除垂体中较短外,所有脑区中MeHg的半衰期约为37天。随着MeHg暴露时间的延长,所有脑区中I-Hg的浓度均升高,尤其是丘脑和垂体。在大多数脑区,6个月和12个月时I-Hg约占T-Hg的9%,18个月时占12%。在垂体中,I-Hg从6个月时占T-Hg的20%增加到18个月时的46%。I-Hg的消除半衰期极长,大多数脑区为230 - 540天,丘脑和垂体中更长。在清除期(6个月)内,丘脑中I-Hg的浓度未降低,而垂体中的I-Hg尽管没有额外暴露仍持续升高。暴露于MeHg的猴子脑中I-Hg浓度比暴露于HgCl2的猴子高几倍,这表明I-Hg是由脑中MeHg的去甲基化形成的,而不是由身体其他部位去甲基化形成的I-Hg被脑摄取。个体猴子之间I-Hg的相对浓度存在很大差异,但脑区之间(除丘脑和垂体外)没有差异。暴露于MeHg的肥胖猴子(体重5.0 - 6.1千克)在所有脑区中MeHg和I-Hg的浓度均高于正常体重猴子,但垂体除外。