碘二醇对实验动物肾脏的影响。

P Walday, I F Heglund, K Golman, J Cornacoff, E Holtz
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引用次数: 21

摘要

本文通过7项独立实验,研究了新型非离子二聚体六碘造影剂(CM)碘沙醇对大鼠、家兔和猴子肾脏功能和形态的影响,并与其他含碘造影剂进行了比较。大鼠5 g I/kg及家兔10.5 g I/kg剂量对血清肌酐水平无显著影响。在与几种CM的比较研究中,当给药10.5 g I/kg和12.5 g I/kg缓慢输注时,兔的蛋白尿立即和短暂增加。注射12.5 g I/kg后血清碘浓度测定显示血清消除半衰期增加。在本研究中,高剂量碘二醇对蛋白尿和消除半衰期的影响与单体非离子CM相同,但不如单体离子CM明显。雄性大鼠在静脉注射碘沙醇或iopamidol (2g I/kg)前4周行单侧肾切除术,可引起肾功能下降。CM的管理不影响肾功能监测血清肌酐和尿素浓度。研究了不同剂量碘沙醇和碘曲兰给药48小时后大鼠肾近端小管细胞空泡化和肾碘潴留的变化。两种CM的空泡化无效应水平均为0.5 g /kg。雄性大鼠的碘潴留率高于雌性大鼠,在2个最高剂量水平(3和5 g I/kg)下,碘沙醇的碘潴留率高于碘曲兰。在其他剂量水平(0.25-1g I/kg)下,碘潴留无差异。研究了雄性大鼠(1.2 g I/kg)和猴子(1.2和3.6 g I/kg)给予碘沙醇后肾近端小管空泡化的可逆性。大鼠的空泡化比猴子更明显。在给药3周后,所有大鼠的空泡化完全逆转,在给药1.2 g I/kg后3天,3只猴子中的2只完全逆转。静脉注射3.5 g /kg碘沙醇14天后,猴子肾脏经皮活检标本的空泡化程度与对照动物无显著差异。综上所述,碘二沙醇对肾功能的影响程度与非离子单体和二聚体比较介质相同,但低于离子单体。碘沙醇诱导的肾近端小管细胞空泡化程度似乎是物种依赖的,在猴子中比在大鼠中更不明显,而且逆转得更快。
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Renal effects of iodixanol in experimental animals.

The effects of the new nonionic dimeric hexa-iodinated contrast media (CM) iodixanol on renal function and morphology were investigated in 7 independent studies in rats, rabbits and monkeys and compared with other iodinated CM. No significant effect on serum creatinine levels was seen at doses up to and including 5 g I/kg in rats and 10.5 g I/kg in rabbits. An immediate and transient increase in proteinuria was found in rabbits when 10.5 g I/kg was administered as a bolus, and when 12.5 g I/kg was administered as a slow infusion in a comparative study with several CM. Increased serum elimination half-life was shown by measuring serum iodine concentrations after the infusion of 12.5 g I/kg. The effect of a high dose of iodixanol on proteinuria and elimination half-life were in this study in the same range as those of the monomeric nonionic CM, but less pronounced than those of the monomeric ionic CM. Reduced renal capacity was induced in male rats by performing unilateral nephrectomy 4 weeks before i.v. injection of iodixanol or iopamidol (2g I/kg). The administration of CM did not affect renal function monitored as serum concentrations of creatinine and urea. The vacuolation of renal proximal tubular cells and kidney iodine retention were investigated in rats 48 hours after administration of different doses of iodixanol or iotrolan. The no-effect level for vacuolation was 0.5 g I/kg for both CM. Iodine retention was higher in male than females rats, and was higher for iodixanol than iotrolan at the 2 highest dose levels (3 and 5 g I/kg). No difference in iodine retention was found at the other dose levels (0.25-1g I/kg). The reversibility of renal proximal tubular vacuolation after administration of iodixanol was studied in male rats (1.2 g I/kg) and monkeys (1.2 and 3.6 g I/kg). The vacuolation was more pronounced in rats than in monkeys. Vacuolation was completely reversed in all rats 3 weeks after dosing, and 2 of 3 monkeys 3 days after a dose of 1.2 g I/kg. The degree of vacuolation evident in renal percutaneous biopsy specimens from monkeys 14 days after i.v. administration of iodixanol at a dose of 3.5 g I/kg was not significantly different to that in control animals. In conclusion, iodixanol affected renal function to the same degree as did the nonionic monomeric and dimeric comparative media, but to a lesser degree than the ionic monomers. The degree of renal proximal tubular cell vacuolation induced by iodixanol seems to be species-dependent, being less pronounced and more quickly reversed in monkeys than rats.

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