类固醇-西罗莫司联合用药对大鼠包膜性腹膜硬化实验模型的影响

S. Ersan, A. Çelik, A. Celik, S. Ada, M. Unlu, T. Köse, S. Sarıoğlu, T. Camsari
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摘要

目的:囊性腹膜硬化(EPS)是腹膜透析的一种破坏性并发症,最终以腹膜硬化和肠袢茧化而告终。哺乳动物雷帕霉素靶点(mTOR)抑制剂依维莫司和西罗莫司在实验动物模型中有减弱EPS的发现。西罗莫司与类固醇联合使用的效果尚未见文献报道。本研究旨在探讨西罗莫司联合类固醇对实验性硬化性腹膜炎模型的影响。材料与方法:41只雄性wistar白化大鼠分为6组:对照组(C组;腹腔注射等渗生理盐水),葡萄糖酸氯己定组(CG;模型组)、休息组(R;CG后腹腔休息,强的松龙组(P;CG组再为强的松龙组,西罗莫司组(Sir;CG组为西罗莫司组,泼尼松龙-西罗莫司组(P-Sir;CG然后是强的松龙加西罗莫司)。在研究结束时牺牲后获得的腹膜标本在光镜下检查腹膜厚度、纤维化和血管强度。结果:与C、P、Sir、P-Sir组相比,CG组和R组腹膜壁层和内脏层厚度、纤维化评分和血管强度均显著增加(P <0.05)。研究结束时,C组、P组、Sir组和P-Sir组的参数没有差异。P组、Sir组和P-Sir组间差异无统计学意义。静息对EPS参数的衰减无效。结论:在本研究中,我们观察到西罗莫司-泼尼松龙联合治疗实验性EPS模型与泼尼松龙和西罗莫司单独治疗方案同样有效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Effect of Steroid-Sirolimus Combination on the Experimental Model of Encapsulating Peritoneal Sclerosis in Rats
ABS TRACT Objective: Encapsulating peritoneal sclerosis (EPS) is a devastating complication of peritoneal dialysis terminating with peritoneal sclerosis and coccooning of intestinal loops. The inhibitors of mammalian target of rapamycin (mTOR), everolimus and sirolimus, have attenuated EPS findings in experimental animal models. The effect of combination of sirolimus with steroid has not been documented so far. The aim of the study was to determine the effect of combination of sirolimus and steroid on experimental sclerosing peritonitis model. Material and Methods: 41 wistar albino male rats were divided into 6 groups : control group (C; isotonic saline injected intraperitoneally), chlorhexidine gluconate group (CG; model group), resting group (R; CG then peritoneal rest, prednisolone group (P; CG then prednisolone), sirolimus group (Sir; CG then sirolimus), and prednisolone-sirolimus group (P-Sir; CG then prednisolone plus sirolimus). Peritoneal specimens obtained after sacrification at the end of study were examined for peritoneal thickness, fibrosis, and vascular intensities under light microscopy. Results: In the CG and R groups there was a significant increase in peritoneal thickness, fibrosis score and vascular intensity compared to C, P, Sir, and P-Sir groups in both parietal and visceral peritoneum (p<0.05). The parameters at the end of the study were not different in C, P, Sir, and P-Sir groups. The difference between P, Sir, and P-Sir groups were not significant. Resting was shown to be ineffective in attenuating EPS parameters. Conclusion: In this study we observed that sirolimus-prednisolone combination was equally effective in experimental EPS model compared to prednisolone and sirolimus only regimens.
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