From GE Healthcare, The Grove Centre (GC18), White Lion Rd, Amersham HP7 9LL, England (A.P.L.S., P.M.E.); GE Global Research Centre, Niskayuna, NY (M.M., J.R., J.M.C., J.C., L.L., C.M.); and GE Healthcare, Life Sciences, Marlborough, Mass (M.G.H.).
Radiology. 2017 Mar;282(3):743-751. doi: 10.1148/radiol.2016160905. Epub 2016 Sep 27.
Purpose To measure the levels of gadolinium present in the rat brain 1 and 20 weeks after dosing with contrast agent and to determine if there are any histopathologic sequelae. Materials and Methods The study was approved by the GE Global Research Center Institutional Animal Care and Use Committee. Absolute gadolinium levels were quantified in the blood and brains of rats 1 week after dosing and 20 weeks after dosing with up to 20 repeat doses of gadodiamide (cumulative dose, 12 mmol per kilogram of body weight) by using inductively coupled plasma-mass spectrometry. Treatment groups (n = 6 rats per group) included low-dosage and high-dosage gadodiamide and osmolality-matched saline controls. Brain sections were submitted (blinded) for standard toxicology assessment per Registry of Industrial Toxicology Animal data guidelines. Analysis of variance and Mann-Whitney U tests with post hoc correction were used to assess differences in absolute gadolinium levels and percentage of injected dose, respectively. Results Dose-dependent low levels of gadolinium were detected in the brain, a mean ± standard deviation of 2.49 nmol per gram of brain tissue ± 0.30 or 0.00019% of the injected dose 1 week after dosing. This diminished by approximately 50% (to 1.38 nmol per gram of brain tissue ± 0.10 or 0.00011% of the injected dose) 20 weeks after dosing. As a percentage of injected dose, the levels of gadolinium measured were comparable between different doses, indicating that mechanisms of uptake and elimination were not saturated at the tested doses. There were no histopathologic findings associated with the levels of gadolinium measured. Conclusion Low levels of gadolinium are present in the brain after repeat dosing with gadodiamide, which is partially cleared over 20 weeks with no detectable neurotoxicity.
测量大鼠在给予造影剂后 1 周和 20 周时大脑中的钆含量,并确定是否存在任何组织病理学后遗症。
本研究得到了通用电气全球研究中心机构动物护理和使用委员会的批准。通过电感耦合等离子体质谱法,在大鼠给予造影剂后 1 周和 20 周时(累计剂量为 12mmol/kg 体重),定量测量血液和大脑中的绝对钆含量。处理组(每组 6 只大鼠)包括低剂量和高剂量的钆喷酸葡胺以及渗透压匹配的生理盐水对照。根据工业毒理学动物数据登记处的指导原则,提交(盲法)脑切片进行标准毒理学评估。使用方差分析和曼-惠特尼 U 检验(事后校正)分别评估绝对钆含量和注射剂量百分比的差异。
在大脑中检测到剂量依赖性的低水平的钆,给药后 1 周时平均值±标准偏差为 2.49nmol/克脑组织±0.30,或注射剂量的 0.00019%。20 周后,这一数值减少了约 50%(至 1.38nmol/克脑组织±0.10,或注射剂量的 0.00011%)。作为注射剂量的百分比,测量的钆水平在不同剂量之间相当,表明在测试剂量下,摄取和消除机制没有饱和。没有与测量的钆水平相关的组织病理学发现。
在重复给予钆喷酸葡胺后,大脑中存在低水平的钆,这些钆在 20 周内部分清除,没有可检测到的神经毒性。