Osuna O, Edds G T
Am J Vet Res. 1982 Aug;43(8):1380-6.
Observations on the interactions of cadmium (Cd) x aflatoxin B1 (AFB1) and Cd x warfarin included several variables of animal performance and hematology. Cadmium was fed daily for 40 days (groups IV, V, VI) and a Cd-free diet was fed to groups I, II, and III. Groups II and V were treated with AFB1, and groups III and VI were treated with warfarin--each for 5 days during the 5th week of the experiment and the effects were observed for 10 days. All pigs fed the diet with added Cd had developed severe anemia by the 4th week of the experiment. The incorporation of this toxic concentration of Cd (83 micrograms/g) in the diet seemed to have blocked the liver microsomal enzyme system (cytochrome P-450), diminishing the toxic effects of 5 daily oral doses (0.2 mg/kg of body wt) of AFB1 (group V pigs), but enhancing synergistically the toxic anticoagulant effects of the same doses of warfarin in young pigs (group VI). The data presented also indicated that the feeding of toxic concentrations of Cd stimulated increased glutathione peroxidase activity, which conjugated the AFB1 epoxides with their excretion as reduced glutathione but enhanced the toxic anticoagulant effects of warfarin in young pigs.
关于镉(Cd)与黄曲霉毒素B1(AFB1)以及镉与华法林相互作用的观察包括动物性能和血液学的几个变量。给IV、V、VI组每日喂食镉,持续40天,给I、II、III组喂食不含镉的饲料。在实验的第5周,给II组和V组用AFB1处理,给III组和VI组用华法林处理,均处理5天,并观察10天的效果。到实验第4周时,所有喂食添加了镉的饲料的猪都出现了严重贫血。饲料中这种有毒浓度的镉(83微克/克)的掺入似乎阻断了肝脏微粒体酶系统(细胞色素P - 450),减轻了5次每日口服剂量(0.2毫克/千克体重)的AFB1对V组猪的毒性作用,但协同增强了相同剂量的华法林对幼猪的毒性抗凝作用(VI组)。所呈现的数据还表明,喂食有毒浓度的镉会刺激谷胱甘肽过氧化物酶活性增加,该酶将AFB1环氧化物与还原型谷胱甘肽结合并排出,但增强了华法林对幼猪的毒性抗凝作用。