Suppr超能文献

慢性肾衰竭大鼠的比较及作为高磷血症模型的制备方案的改进

Comparison of chronic renal failure rats and modification of the preparation protocol as a hyperphosphataemia model.

作者信息

Terai Kazuhiro, Mizukami Kazuhiko, Okada Masamichi

机构信息

Kidney and Digestive Tracts Laboratory, Institute of Pharmacology, Astellas Pharma Co. Ltd, Miyukigaoka, Tsukuba, Ibaraki, Japan.

出版信息

Nephrology (Carlton). 2008 Apr;13(2):139-46. doi: 10.1111/j.1440-1797.2007.00844.x.

Abstract

BACKGROUND

Several animal models with chronic renal failure have been established and used for demonstrating complications including hyperphosphataemia. Although long-time feeding is required to cause hyperphosphataemia in animals, a few modifications have been reported to provide more useful models for research.

METHODS

Three separate experiments were carried out in the present study. First, characteristics of commonly used subnephrectomized (5/6Nx) rats and rats fed an adenine diet (0.75% adenine in normal diet) were compared as hyperphosphataemia models. Next, using adenine-diet rats, the inhibitory effect of sevelamer hydrochloride (Sev) on serum phosphorus elevation was examined. Third, oral adenine dosing for induction of hyperphosphataemia and validation as a model using Sev were examined.

RESULTS

Serum phosphorus in 5/6Nx rats became elevated in 8-17 weeks, but the levels and time points of elevation differed among animals. In adenine-fed rats, the elevation was more clearly demonstrated with less diversity at 4 weeks. The data revealed a potential shorter model preparation period and the importance of controlling feeding amounts. Oral adenine dosing induced hyperphosphataemia by 12 days, and Sev treatment was inhibitory. After a maintenance period of over a month (no treatments), Sev-treated rats showed hyperphosphataemia as did oral adenine-dosed control rats. The serum phosphorus levels significantly decreased on further Sev treatment.

CONCLUSION

Oral dosing with adenine made the model preparation period definitely shorter, and its usefulness as a hyperphosphataemia model was revealed using Sev.

摘要

背景

已经建立了几种慢性肾衰竭动物模型,并用于证明包括高磷血症在内的并发症。尽管在动物中需要长时间喂食才能导致高磷血症,但据报道一些改进方法可提供更有用的研究模型。

方法

本研究进行了三项独立实验。首先,比较常用的肾次全切除(5/6Nx)大鼠和喂食腺嘌呤饮食(正常饮食中含0.75%腺嘌呤)的大鼠作为高磷血症模型的特征。其次,使用喂食腺嘌呤饮食的大鼠,研究盐酸司维拉姆(Sev)对血清磷升高的抑制作用。第三,研究口服腺嘌呤诱导高磷血症并验证其作为使用Sev的模型的有效性。

结果

5/6Nx大鼠的血清磷在8 - 17周时升高,但升高水平和时间点在动物之间有所不同。在喂食腺嘌呤的大鼠中,4周时升高更明显,且差异较小。数据显示模型制备期可能更短以及控制喂食量的重要性。口服腺嘌呤给药12天后诱导出高磷血症,Sev治疗具有抑制作用。经过一个多月的维持期(无治疗)后,接受Sev治疗的大鼠与口服腺嘌呤给药的对照大鼠一样出现高磷血症。进一步进行Sev治疗后,血清磷水平显著下降。

结论

口服腺嘌呤使模型制备期明显缩短,并且使用Sev揭示了其作为高磷血症模型的有效性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验