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Experimental Peritoneal Sclerosis Models Should Not Be Based on Chlorhexidine Gluconate Anymore

机译:实验性腹膜硬化模型不应再以葡萄糖酸氯己定为基础

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Background/Aims: Currently available rodent models of peritoneal sclerosis are not based on clinically relevant factors: renal failure in combination with exposure to bioincompatible fluids. Our aim was to develop a chronic peritoneal infusion model of peritoneal sclerosis in rats with renal failure. Methods: Male Wistar rats underwent a catheter implantation and a 70% nephrectomy. They were randomly divided into three peritoneal infusion groups: chlorhexidine gluconate/ethanol (CGE) + Dianeal (Baxter Healthcare, Cas-tlebar, Ireland), CGE + buffer (Physioneal without glucose; Baxter, Nivelles, Belgium) and Dianeal alone. After 8 weeks a peritoneal permeability test was performed and omental tissue was obtained for morphometrics. Results: The CGE + Dianeal group (n = 6) and CGE + buffer (n = 6) group showed high peritoneal clearances of small solutes and proteins, ul-trafiltration failure, impaired free water transport, severe fi-brosis and high vessel counts, but the groups did not differ significantly. The Dianeal group (n = 6) showed significantly lower clearances of small solutes and proteins, normal ultra-filtration and sodium sieving, and significantly lower fibrosis scores and vessel counts. Conclusions: Abnormalities seen in peritoneal sclerosis can be induced in a peritoneal infusion model in rats with renal failure. However, the addition of a bioincompatible dialysis solution had no contributing role, probably because the effects were overruled by those of CGE.
机译:背景/目的:目前可获得的腹膜硬化的啮齿动物模型并非基于临床相关因素:肾功能衰竭与暴露于生物不相容性液体的结合。我们的目的是建立肾衰竭大鼠腹膜硬化的慢性腹膜灌注模型。方法:雄性Wistar大鼠进行了导管植入和70%肾切除术。他们被随机分为三个腹膜输注组:葡萄糖酸氯己定/乙醇(CGE)+ Dianeal(爱尔兰的Cas-tlebar,Baxter Healthcare),CGE +缓冲液(不含葡萄糖的Physioneal; Baxter,Nivelles,比利时)和单独的Dianeal。 8周后,进行腹膜通透性测试并获得网膜组织以进行形态计量学。结果:CGE + Dianeal组(n = 6)和CGE +缓冲液(n = 6)组显示高的腹膜清除率,小的溶质和蛋白质,超滤失败,自由水运输受损,严重的纤维化和高血管计数,但各组之间没有显着差异。 Dianeal组(n = 6)显示小溶质和蛋白质的清除率明显降低,超滤和钠筛分正常,纤维化评分和血管计数明显降低。结论:肾功能衰竭大鼠腹腔输注模型可诱发腹膜硬化异常。但是,添加生物不相容性透析液没有贡献作用,这可能是因为CGE的效果无法实现。

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