Suzuki S, Taguchi T
J Toxicol Environ Health. 1980 Jul;6(4):783-96. doi: 10.1080/15287398009529897.
Retention, excretion, and organ distribution of radioactive Cd were observed after a single oral dose of two monkeys. The retention rate of Cd 19 d after the administration of radiocadmium (109CdCl2, carrier-free) to one monkey was 5.2% of the administered dose; 73.4% of the dose was excreted in the feces and 0.7% in the urine. The largest fractions of the administered dose were found in the small intestine, liver, and kidney. The absorption rate of Cd 25 d after the administration of radiocadmium with 1.0 mg cold Cd as CdCl2 solution to the othermonkey was 6.3% of the administered dose; 75.5% of the dose was excreted in the feces and 0.9% in the urine. Setting the whole body retention equal to 100% on d 19 or 25, the largest fractions were found in the small intestines (51.5 and 36.3%), livers (21.8 and 29.6%), and kidneys (13.4 and 21.0%) of the respective monkeys). The effect of carrier Cd on absorption, excretion, and organ distribution was not pronounced. The highest concentration and greatest retention of Cd was observed in the upper small intestinal wall and the content of the small intestine, indicating the importance of enteroenteric circulation of the element; this finding was different from the results for Cd metabolism in rodents.
给两只猴子单次口服给药后,观察了放射性镉的滞留、排泄及在器官中的分布情况。给一只猴子口服无载体放射性镉(109CdCl2)19天后,镉的滞留率为给药剂量的5.2%;73.4%的剂量经粪便排出,0.7%经尿液排出。给药剂量中最大部分分布在小肠、肝脏和肾脏。给另一只猴子以氯化镉溶液形式口服含1.0毫克非放射性镉的放射性镉25天后,镉的吸收率为给药剂量的6.3%;75.5%的剂量经粪便排出,0.9%经尿液排出。在第19天或第25天将全身滞留量设定为100%时,在相应猴子的小肠(分别为51.5%和36.3%)、肝脏(分别为21.8%和29.6%)和肾脏(分别为13.4%和21.0%)中发现了最大部分。载体镉对吸收、排泄和器官分布的影响不明显。在小肠上段肠壁和小肠内容物中观察到镉的最高浓度和最大滞留量,表明该元素肠肝循环的重要性;这一发现与啮齿动物中镉代谢的结果不同。