Cherian M G, Vostal J J
J Toxicol Environ Health. 1977 Mar;2(4):945-54. doi: 10.1080/15287397709529493.
Biliary excretion of cadmium was studied in rats after intravenous injection of different doses of cadmium chloride (0.1-2 mg Cd/kg). The rate of bile flow was not affected by cadmium injection and cadmium was excreted into bile during the first 2 hr after injection. The biliary excretion of cadmium increased with increasing dose of CdCl2. Cumulative biliary excretion of cadmium for 5 hr was 0.065% of the administered dose for groups injected with 0.1 mg Cd/kg as compared to 16.9% of the administered dose for 2 mg Cd/kg. During the 5 hr experimental period, most of the cadmium in liver cytosol was bound to high-molecular-weight proteins and less than 10% was bound to the metallothionein fraction. The biliary cadmium was recovered as a low-molecular-weight compound (less than 4,000) in experiments with various doses of cadmium and no cadmium was attached to high-molecular-weight proteins or metallothionein in the bile. The low-molecular-weight cadmium complex in bile was partially characterized as Cd-glutathione by thin-layer chromatography and amino acid analysis.
在给大鼠静脉注射不同剂量的氯化镉(0.1 - 2毫克镉/千克)后,研究了镉的胆汁排泄情况。胆汁流速不受镉注射的影响,并且在注射后的最初2小时内镉排泄到胆汁中。镉的胆汁排泄量随氯化镉剂量的增加而增加。对于注射0.1毫克镉/千克的组,5小时内镉的累积胆汁排泄量为给药剂量的0.065%,而对于注射2毫克镉/千克的组,该比例为给药剂量的16.9%。在5小时的实验期内,肝细胞质溶胶中的大部分镉与高分子量蛋白质结合,与金属硫蛋白部分结合的镉不到10%。在不同剂量镉的实验中,胆汁中的镉以低分子量化合物(小于4000)形式回收,并且胆汁中没有镉与高分子量蛋白质或金属硫蛋白结合。通过薄层色谱和氨基酸分析,胆汁中的低分子量镉复合物部分被鉴定为镉 - 谷胱甘肽。