Shaikh Z A, Smith J C
Chem Biol Interact. 1976 Dec;15(4):327-36. doi: 10.1016/0009-2797(76)90138-1.
The biosynthesis of the cadmium-binding protein, metallothionein, was studied in rat liver and kidney after injection of cadmium chloride. A simplified procedure for the isolation of metallothionein from liver and kidney tissues was devised. It was found that the concentration of a subcutaneously injected dose of 30 mumoles of 109CdCl2/kg in the liver reached the maximum within 36 h. Thereafter, a slow decrease in the concentration of the isotope was noted during the 3 week period. In the kidney, the isotope was taken up in two phases. During the first phase the uptake was faster and lasted for about 4 days. The second phase of 109Cd accumulation showed a slower increase in the concentration oe 109Cd was associated with metallothionein. Amino acid incorporation studies revealed that active biosynthesis of metallothionein took place in the kidney as well as in the liver of cadmium-exposed rats. The turnover of 35S-labeled metallothionein was also investigated and the half-lives of the hepatic and the renal metallothionein were found to be 2.8 and 5 days, respectively.
在给大鼠注射氯化镉后,对其肝脏和肾脏中镉结合蛋白金属硫蛋白的生物合成进行了研究。设计了一种从肝脏和肾脏组织中分离金属硫蛋白的简化程序。结果发现,皮下注射剂量为30微摩尔/千克的109CdCl2在肝脏中的浓度在36小时内达到最大值。此后,在3周内该同位素的浓度缓慢下降。在肾脏中,同位素的摄取分为两个阶段。在第一阶段,摄取速度较快,持续约4天。109Cd积累的第二阶段显示,109Cd浓度的增加较为缓慢,且与金属硫蛋白有关。氨基酸掺入研究表明,在镉暴露大鼠的肾脏和肝脏中均发生了金属硫蛋白的活跃生物合成。还研究了35S标记的金属硫蛋白的周转情况,发现肝脏和肾脏中金属硫蛋白的半衰期分别为2.8天和5天。