Bjondahl K
Med Biol. 1976 Dec;54(6):454-60.
Pretreatment with nafenopin and pregnenolone-16-alpha-carbonitrile (PCN) decreased the acute lethal toxicity in mice induced by cerium chloride (12 mg/kg resp. 15 mg/kg). Treatment with nafenopin and PCN increased the relative liver weight. More cerium accumulated in the liver of nafenopin- and PCN-treated animals than in controls during the first hours after injection. After 14 days the amount of cerium in the livers of nafenopin-treated animals was significantly higher. The concentration of cerium as a percentage of the injected dose calculated per mg liver was lower during the first day in the nafenopin group and higher in the PCN group than in the control group. After 6 days cerium concentration decreased significantly less in the livers of the nafenopin group. Cerium concentration in the blood was significantly lower in the nafenopin group during the first day. Only small amounts of the injected cerium were excreted in the urine, and no difference between treated and untreated animals was found. The amount of cerium excreted in faeces was somewhat smaller in the nafenopin-treated animals during the whole experiment.
用萘芬诺平及孕烯醇酮 -16-α- 腈(PCN)进行预处理可降低氯化铈(分别为 12 毫克/千克和 15 毫克/千克)诱导的小鼠急性致死毒性。用萘芬诺平和 PCN 进行处理可增加肝脏相对重量。在注射后的最初几小时内,萘芬诺平和 PCN 处理组动物肝脏中积累的铈比对照组更多。14 天后,萘芬诺平处理组动物肝脏中的铈含量显著更高。以每毫克肝脏计算,萘芬诺平组在第一天铈的浓度占注射剂量的百分比低于对照组,而 PCN 组则高于对照组。6 天后,萘芬诺平组肝脏中铈浓度的下降明显较少。第一天,萘芬诺平组血液中的铈浓度显著较低。仅少量注射的铈从尿液中排出,未发现处理组和未处理组动物之间存在差异。在整个实验过程中,萘芬诺平处理组动物粪便中排出的铈量略少。