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在动物模型中,腹腔内注射大剂量基于钆的造影剂不会导致肾源性系统性纤维化。

In an animal model nephrogenic systemic fibrosis cannot be induced by intraperitoneal injection of high-dose gadolinium based contrast agents.

机构信息

Medicine and Health Sciences (FMHS), United Arab Emirates University, Al Ain, United Arab Emirates.

出版信息

Eur J Radiol. 2012 Oct;81(10):2562-7. doi: 10.1016/j.ejrad.2011.10.032. Epub 2012 Feb 1.

Abstract

AIM AND OBJECTIVE

Nephrogenic systemic fibrosis (NSF) has been reported in humans to be most likely induced by gadolinium based contrast agents (GBCA), namely by gadodiamide, gadopentetate dimeglumine, and gadoversetamide, rarely by other GBCA. The pathogenesis of NSF remains unclear; different hypotheses are under discussion. The objective of the study is to assess if in the animal model human-like NSF changes can be induced by high-dose, intraperitoneal GBCA injections over four weeks.

MATERIALS AND METHODS

After approval by the institutional animal ethics committee, six rats each were randomly assigned to groups, and treated with seven different GBCA. Intraperitoneal (IP) injections - proven in the animal model to be effective - were chosen to prolong the animals' exposure to the respective GBCA. GBCA doses of previous intravenous (IV) animal studies were applied. After five weeks all rats were sacrificed. Sham controls were treated with IP saline injections, employing the same regimen.

RESULTS

No findings comparable with human NSF were observed in all animals after IP treatment with all seven GBCA at daily doses of 2.5 and 5.0 mmol/kg body weight (BW). No histopathological abnormalities of all examined organs were noted. Weight loss was stated in weeks three and four with GBCA injections at doses of 5.0 mmol/kg BW, but rats regained weight after cessation of GBCA treatment.

CONCLUSIONS

NSF-comparable pathological findings could not be induced by high dose intraperitoneal injection of seven GBCA.

摘要

目的和目标

已在人类中报告,肾源性系统性纤维化(NSF)最有可能由基于钆的造影剂(GBCA)引起,即由钆喷酸葡胺、钆贝葡胺和gadodiamide 引起,很少由其他 GBCA 引起。NSF 的发病机制仍不清楚;正在讨论不同的假设。本研究的目的是评估在动物模型中,高剂量腹腔内 GBCA 注射是否可以在四周内诱导出类似人类的 NSF 变化。

材料和方法

在机构动物伦理委员会批准后,将六只大鼠随机分为每组,并分别用七种不同的 GBCA 进行处理。选择腹腔内(IP)注射-已在动物模型中证明有效-以延长动物接触各自 GBCA 的时间。应用了先前静脉内(IV)动物研究的 GBCA 剂量。五周后,所有大鼠均被处死。假对照采用腹腔内生理盐水注射,采用相同方案。

结果

在所有动物中,用每天 2.5 和 5.0mmol/kg 体重(BW)的七种 GBCA 进行腹腔内治疗后,未观察到与人类 NSF 相媲美的发现。所有检查器官均未发现组织病理学异常。在 5.0mmol/kg BW 剂量的 GBCA 注射后的第三和第四周,体重下降,但在停止 GBCA 治疗后,大鼠体重恢复。

结论

高剂量腹腔内注射七种 GBCA 不能诱导出与 NSF 相媲美的病理发现。

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