Environmental Toxicology Section, Alberta Environmental Centre, Bag 4000, TOB 4L0, Vegreville, Alberta, Canada.
Biol Trace Elem Res. 1986 Jul;10(1):47-63. doi: 10.1007/BF02795318.
Cadmium was administered subcutaneously to male Wistar rats, 0.1 mL/rat in 0.9% saline 3 times a wk for 4 wk at 3 mg Cd/kg. Saline was administered to control animals in an equivalent manner, without Cd. After the end of the dosing period, the distribution and excretion of Cd, Cu, Ca, Zn, and Fe were observed in some organs and excreta for 35 d (1, 7, 14, 21, 28, and 35 d). Cadmium dosing caused significant disturbances in the metabolism of Zn, Cu, Fe, and Ca, especially during the recovery period. Growth in Cd-dosed animals did not accelerate, even after 5 wk of recovery. There was evidence of mobilization of some elements among organs. Accumulation of Cd occurred in liver, kidney, and spleen during dosing, and during the recovery period it was retained in kidney and testes (for 2 wk) and cleared steadily in liver and RBC (for 5 wk), but increased in spleen (first 3 wk). The pattern of Cd excretion was closely associated with the binding of Cd with metallothioneins in kidney and liver for the first 21 and 7 d, respectively. This was associated with the excretion of Cd-metallothioneins (Cd-MT) in urine from d 1 to 21 during recovery. Cadmium caused higher Ca accumulations in testes and liver, which were probably associated with the lesions observed in these organs. Significant increases of Cu (in kidney d 7) and Fe (in liver) were observed during recovery. Furthermore, significant reductions of Cu and Fe were found in plasma, spleen, and RBC (after 5 wk) and kidney, spleen, and testes (on d 7), and blood (after 5 wk).
给雄性 Wistar 大鼠皮下注射 0.1 mL/只 0.9%生理盐水,每周 3 次,共 4 周,剂量为 3 mg Cd/kg。以相同方式向对照动物给予生理盐水,不给予 Cd。给药期结束后,观察 Cd、Cu、Ca、Zn 和 Fe 在某些器官和排泄物中的分布和排泄情况,为期 35 天(1、7、14、21、28 和 35 天)。Cd 给药导致 Zn、Cu、Fe 和 Ca 的代谢明显紊乱,尤其是在恢复期。即使在 5 周的恢复期后,Cd 处理动物的生长也没有加速。有证据表明,器官之间存在某些元素的动员。在给药期间,Cd 在肝脏、肾脏和脾脏中积累,在恢复期,它在肾脏和睾丸中保留(2 周),并在肝脏和 RBC 中稳定清除(5 周),但在脾脏中增加(前 3 周)。Cd 排泄模式与 Cd 与肾和肝中金属硫蛋白的结合密切相关,分别在第 21 和 7 天。这与恢复期第 1 至 21 天尿中 Cd-金属硫蛋白(Cd-MT)的排泄有关。Cd 导致睾丸和肝脏中 Ca 积累增加,这可能与这些器官中观察到的病变有关。在恢复期观察到 Cu(肾脏第 7 天)和 Fe(肝脏)显著增加。此外,在恢复期,还发现血浆、脾脏和 RBC(5 周后)以及肾脏、脾脏和睾丸(第 7 天)和血液(5 周后)中的 Cu 和 Fe 显著减少。