Cikrt M, Tichý M
J Hyg Epidemiol Microbiol Immunol. 1980;24(3):346-55.
Wistar strain female rats were used to study the impact of 1-cysteine,D,L-penicillamine, EDTA, sodium N,N-diethyldithiocarbamate, BAL, Unitiou, Spironolactone, Thiomestron and thiophenolacetate on excretion kinetics and distribution pattern of 203Hg injected intravenously in a dose of 120 microgram 203Hg2+ per rat. A considerably enhanced biliary excretion of mercury was observed after pretreatment with Spironolactone, Unitiol, BAL and Thiomestron. The action of these agents persisted for only 2--3 hours after mercury application. The highest urinary excretion of mercury was recorded after pretreatment with Unitol and BAL. All the tested agents, particularly thiophenolacetate, turned out to enhance mercury excretion through intestinal wall cells. Pretreatment with the tested agents caused also considerable changes in the pattern of mercury distribution in the rat organism.
选用Wistar品系雌性大鼠,研究1-半胱氨酸、DL-青霉胺、乙二胺四乙酸(EDTA)、N,N-二乙基二硫代氨基甲酸钠、二巯丙醇(BAL)、二巯基丙磺酸钠(Unitiol)、螺内酯、硫美雌醇和硫代苯乙酸酯对每只大鼠静脉注射120微克203Hg2+形式的203Hg排泄动力学及分布模式的影响。用螺内酯、二巯基丙磺酸钠、二巯丙醇和硫美雌醇预处理后,观察到汞的胆汁排泄显著增强。这些药物的作用在汞注入后仅持续2至3小时。用二巯基丙磺酸钠和二巯丙醇预处理后,汞的尿排泄量最高。所有受试药物,尤其是硫代苯乙酸酯,均能增强汞通过肠壁细胞的排泄。用受试药物预处理也会使大鼠体内汞的分布模式发生显著变化。