Zhao J Y, Foulkes E C, Jones M
Department of Environmental Health, University of Cincinnati, College of Medicine, OH 45267-0056.
Toxicology. 1990 Dec 3;64(3):235-43. doi: 10.1016/0300-483x(90)90116-x.
A single injection of CdCl2 (15 mumol/kg) together with 300 mumol/kg mercaptoethanol into adult male rats induced renal dysfunction only after a delay of at least 12 h; in contrast, the peak value of cadmium in renal cortex (34 +/- 3 micrograms/g) was reached within 2 h. The chelator methoxybenzylglucaminedithioate (MBGDT) rapidly reduced the renal Cd level by 2/3, primarily by extracting the metal from the sedimentable rather than the cytosolic fraction. MBGDT prevented the subsequent onset of malfunction, but only when given at an early stage after Cd administration (2 h). It follows that the renal damage seen after the initiation period is independent of the Cd concentration at that time. The changes occurring during initiation remain unexplained.
给成年雄性大鼠单次注射氯化镉(15微摩尔/千克)并同时注射300微摩尔/千克巯基乙醇,至少延迟12小时后才会引发肾功能障碍;相比之下,肾皮质中的镉在2小时内就达到了峰值(34±3微克/克)。螯合剂甲氧基苄基葡糖胺二硫代酸酯(MBGDT)迅速使肾脏镉水平降低了2/3,主要是通过从可沉淀部分而非胞质部分提取金属。MBGDT可预防随后出现的功能障碍,但仅在镉给药后的早期阶段(2小时)给药才有效。由此可见,起始期后出现的肾损伤与当时的镉浓度无关。起始期发生的变化仍无法解释。