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碘海醇与碘克沙醇对肾脏的毒性作用比较

Comparative toxic effects of iobitridol and iohexol on the kidney.

作者信息

Wasaki M, Kawamura H, Sugimoto J, Shimada M, Satoh Y, Tanaka E, Gemba M

机构信息

Toxicology Laboratory, Yokohama Research Center, Mitsubishi Chemical Co., Japan.

出版信息

Invest Radiol. 1998 Jul;33(7):393-400. doi: 10.1097/00004424-199807000-00003.

Abstract

RATIONALE AND OBJECTIVES

The authors compare the toxic effects of iobitridol and iohexol, which are nonionic contrast media with equivalent osmolalities and viscosities on the kidney.

METHODS

In a rat acute renal failure (ARF) model, iobitridol or iohexol (both at the dose of 2.87 g I/kg) were injected to rats after pretreatment with indomethacin and N omega-nitro-L-arginin methyl ester. The effects on histopathology, creatinine clearance, and urinary N-acethyl-beta-D-glucosaminidase (NAG) activity were assessed. In a rat renal slice system, the slices were exposed to iobitridol or iohexol (both at the concentration range of 17.5-70 mg iodine/mL) for 60 min. The accumulation of para-aminohippuric acid (PAH), an organic anion, and the intracellular potassium content as the indicators of renal tubular injury were measured to assess the direct effects of iobitridol and iohexol on renal tubules.

RESULTS

In the ARF model, no significant difference was detected between the effects of iobitridol and those of iohexol on the creatinine clearance and urinary NAG activity 24 hours after the injection. However, iobitridol produced a lower degree and incidence of renal tubular injury of renal proximal tubules (P < 0.001) and distal tubules (P < 0.05) compared with iohexol. In the rat renal slice system, the iobitridol treatment had significantly less effect on the PAH accumulation compared with iohexol (P < 0.001). There were no changes in the intracellular potassium content.

CONCLUSIONS

These findings suggest that iobitridol has significantly less toxic effects on the kidney compared with iohexol under the condition of our experiment.

摘要

原理与目的

作者比较了碘比醇和碘海醇的毒性作用,这两种非离子型造影剂具有相同的渗透压和粘度,且均作用于肾脏。

方法

在大鼠急性肾衰竭(ARF)模型中,在使用吲哚美辛和N-ω-硝基-L-精氨酸甲酯预处理后,将碘比醇或碘海醇(剂量均为2.87 g I/kg)注射给大鼠。评估其对组织病理学、肌酐清除率和尿N-乙酰-β-D-氨基葡萄糖苷酶(NAG)活性的影响。在大鼠肾切片系统中,将切片暴露于碘比醇或碘海醇(浓度范围均为17.5 - 70 mg碘/mL)中60分钟。测量对氨基马尿酸(PAH,一种有机阴离子)的积累以及细胞内钾含量作为肾小管损伤的指标,以评估碘比醇和碘海醇对肾小管的直接作用。

结果

在ARF模型中,注射后24小时,碘比醇和碘海醇对肌酐清除率和尿NAG活性的影响之间未检测到显著差异。然而,与碘海醇相比,碘比醇导致的肾近端小管(P < 0.001)和远端小管(P < 0.05)的肾小管损伤程度和发生率更低。在大鼠肾切片系统中,与碘海醇相比,碘比醇处理对PAH积累的影响显著更小(P < 0.001)。细胞内钾含量没有变化。

结论

这些发现表明,在我们的实验条件下,碘比醇对肾脏的毒性作用明显小于碘海醇。

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