203hg -乙基氯化汞分布与排泄的实验研究

E. Ogawa, Shiro Suzuki, H. Tsuzuki, M. Kawajiri
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引用次数: 3

摘要

采用小鼠和大鼠口服203hg -乙基氯化汞,观察其吸收、滞留、排泄和分布情况。吸收:与甲基汞一样,口服给药后吸收相当快。体内滞留量:全身滞留量日递减曲线在大鼠中为两个指数函数之和,在小鼠中为单个指数函数。体内分布:口服给药后3天小鼠和7天大鼠体内203Hg的分布情况。在大鼠中,肾脏的放射性最高,其次是血液、肝脏、脾脏、胰腺和大脑。在小鼠中,肾脏的放射性最高,其次是肝脏、胰腺、脾脏、血液和大脑。排泄:每日203Hg在粪便中高,在尿液中低。服用各种药物的效果。在小鼠3天的实验中,对203Hg的有效清除药物是dl -青霉胺、2-巯基丙酰甘氨酸和谷胱甘肽。BAL、巯基乙酸和硫乙醇均可增加脑内203Hg浓度。在大鼠7天的实验中,BAL和2-巯基丙酰甘氨酸是排203Hg的有效药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
EXPERIMENTAL STUDIES ON THE DISTRIBUTION AND EXCRETION OF 203HG-ETHYLMERCURY CHLORIDE
203Hg-ethylmercury chloride was orally given to mice and rats, and its absorption, retention, excretion and distribution were investigated.1. Absorption : The absorption was considerably fast after the oral administration as in the case of methylmercury.2. Retention in the body : The daily decrement curve of the whole-body retention represents the sum of two exponential functions in rats, but a single expornential function in mice.3. Distribution in the body : The distribution of 203Hg was determined for 3 days with mice and 7 days with rats after the oral administration. In rats, the highest radioactivity was found in the kidney followed by in blood, liver, spleen, pancreas and brain in the descending order. In mice, the highest radioactivity was also found in the kidney, however, next order was the liver, pancreas, spleen, blood and brain successively.4. Excretion : The daily excretion of 203Hg was high in feces and low in urine.5. Effects of administration of various drugs. In 3 day experiments with mice, the effective drugs on eliminating of 203Hg are DL-Penicillamine, 2-mercaptopropionyl glycine and GSH. BAL, Mercaptoacetic acid and Thioethanol were found to increase 203Hg concentration in the brain. In 7 day experiments with rats, the effective drugs in expelling 203Hg were BAL and 2-Mercaptopropionyl glycine.
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