Institut de Radioprotection et de Sûreté Nucléaire (IRSN), PSE-SANTE, SESANE, B.P. N°17, 92262, Fontenay-Aux-Roses Cedex, France.
Institut de Radioprotection et de Sûreté Nucléaire (IRSN), PSE-SANTE, SDOS, Fontenay-aux-Roses, France.
Sci Rep. 2023 Mar 13;13(1):4111. doi: 10.1038/s41598-023-31073-1.
During nuclear fuel processing, workers can potentially be exposed to repeated inhalations of uranium compounds. Uranium nephrotoxicity is well documented after acute uranium intake, but it is controversial after long-term or protracted exposure. This study aims to analyze the nephrotoxicity threshold after repeated uranium exposure through upper airways and to investigate the resulting uranium biokinetics in comparison to reference models. Mice (C57BL/6J) were exposed to uranyl nitrate (0.03-3 mg/kg/day) via intranasal instillation four times a week for two weeks. Concentrations of uranium in urines and tissues were measured at regular time points (from day 1 to 91 post-exposure). At each exposure level, the amount of uranium retained in organs/tissues (kidney, lung, bone, nasal compartment, carcass) and excreta (urine, feces) reflected the two consecutive weeks of instillation except for renal uranium retention for the highest uranium dose. Nephrotoxicity biomarkers, KIM-1, clusterin and osteopontin, are induced from day 4 to day 21 and associated with changes in renal function (arterial fluxes) measured using non-invasive functional imaging (Doppler-ultrasonography) and confirmed by renal histopathological analysis. These results suggest that specific biokinetic models should be developed to consider altered uranium excretion and retention in kidney due to nephrotoxicity. The threshold is between 0.25 and 1 mg/kg/day after repeated exposure to uranium via upper airways.
在核燃料处理过程中,工作人员可能会反复吸入铀化合物。急性铀摄入后,铀肾毒性已有充分的记载,但长期或长期暴露后则存在争议。本研究旨在通过上呼吸道分析反复铀暴露后的肾毒性阈值,并与参考模型相比研究由此产生的铀生物动力学。通过鼻内滴注,每周 4 次,2 周内,将小鼠(C57BL/6J)暴露于硝酸铀酰(0.03-3mg/kg/天)中。定期测量铀在尿液和组织中的浓度(从暴露后第 1 天到第 91 天)。在每个暴露水平下,器官/组织(肾脏、肺、骨、鼻隔室、尸体)和排泄物(尿液、粪便)中保留的铀量反映了两次连续的滴注,除了最高铀剂量的肾脏铀保留。从第 4 天到第 21 天,肾毒性生物标志物 KIM-1、簇蛋白和骨桥蛋白被诱导,并与使用非侵入性功能成像(超声多普勒)测量的肾功能(动脉通量)变化相关,并通过肾脏组织病理学分析得到证实。这些结果表明,应开发特定的生物动力学模型来考虑由于肾毒性而改变的肾脏中铀的排泄和保留。在上呼吸道反复暴露于铀后,阈值在 0.25 至 1mg/kg/天之间。