依那西普对实验性急性肾衰竭的保护作用

Mehmet Kara, Mehmet Fatih Sönmez, Hasan Basri Ulusoy
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摘要

目的:急性肾衰竭(ARF)是一种临床综合征,引起肾小球滤过率下降,导致含氮废物和尿毒症毒素的积累。本研究探讨依那西普对ARF的保护作用。材料与方法:以Balb-C雌性小鼠为实验对象。急性肾衰竭是由腹腔注射叶酸引起的。治疗组依那西普注射叶酸,剂量分别为0.7 mg/kg、3.5 mg/kg和7 mg/kg。在研究第7天测定血尿素氮、肌酐和胱抑素c水平。采用苏木精-伊红染色和Tunel法对肾脏进行组织学检查。结果:依那西普改善叶酸所致肾形态损伤。依那西普组大鼠肾小管细胞凋亡指数较低,扩张程度较轻。叶酸增加了血尿素氮水平。随着依那西普剂量的增加,这种增加逐渐减少。各组肌酐水平无差异。结论:本研究探讨依那西普对急性肾功能衰竭(ARF)的保护作用。结果表明,依那西普能改善叶酸损伤大鼠肾脏形态,降低细胞凋亡指数,并逐渐降低血尿素氮水平。尽管肌酐水平在治疗组之间没有显着差异,但研究结果表明依那西普可能有望成为治疗ARF的潜在药物。需要进一步的研究和临床研究来验证其在人类受试者中的有效性和安全性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Protective Effect of Etanercept in Experimentally Generated Acute Kidney Failure
Objective: Acute renal failure (ARF) is a clinical syndrome that causes a decrease in the glomerular filtration rate and leads to an accumulation of nitrogenous waste products and uremic toxins. This study investigated the protective effect of Etanercept on ARF. Materials and Methods: Experiments were done on Balb-C female mice. Acute renal failure was created with an intraperitoneal folic acid injection. Etanercept was injected with folic acid in doses of 0.7 mg/kg, 3.5 mg/kg, and 7 mg/kg in treatment groups. Blood urea nitrogen levels, creatinine and cystatin-c were measured on the 7th day of the study. The kidneys were examined histologically with hematoxylin-eosin staining and Tunel assay. Results: Etanercept improved kidney morphology damaged by folic acid. The apoptotic index was low, and there was less dilation in the renal tubules in the groups treated with Etanercept. Folic acid increased blood urea nitrogen levels. This increase was decreased gradually with increased doses of Etanercept. There were no differences in creatinine levels in all groups. Conclusion: This study investigated the protective effects of Etanercept in the context of Acute Renal Failure (ARF). The results demonstrated that Etanercept improved kidney morphology damaged by folic acid, reduced the apoptotic index, and gradually decreased elevated blood urea nitrogen levels. Although creatinine levels showed no significant differences among the treatment groups, the findings suggest that Etanercept may hold promise as a potential agent for the treatment of ARF. Further research and clinical studies are warranted to validate its effectiveness and safety in human subjects.
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