新型gatti隐球菌培养滤液治疗实验性免疫复合物肾小球肾炎的新方法

Abbas Mirshafiey, Farhad Mehrabian, Alireza Razavi, Mohammad R Shidfar, Saeed Namaki
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引用次数: 13

摘要

本研究旨在探讨新型隐球菌(CneF)培养滤液对实验性免疫复合物肾小球肾炎的治疗作用。采用皮下免疫和每日静脉注射牛血清白蛋白(BSA)诱导大鼠肾炎。以三种不同剂量(36、54和90mg /kg,基于碳水化合物浓度)的CneF溶液,每隔72小时定期腹腔注射4周。治疗开始于第65天,并在不同时间间隔测量尿蛋白。在第107天对动物实施安乐死。在献祭时测定血清和尿液决定因素,并检查肾脏标本。本实验结果显示,CneF治疗组大鼠尿蛋白排泄量、血尿素氮(BUN)、血浆甘油三酯浓度显著低于对照组,血清高密度脂蛋白胆固醇显著升高。此外,治疗组和未治疗组的肾小球变化也有显著差异。这些观察结果表明,CneF的有益作用可能与肾小球白细胞数量的减少有关。我们的研究结果表明,CneF作为一种新的抗炎化合物可以减少蛋白尿,抑制肾小球病变的发展,并在免疫复合物肾小球肾炎大鼠模型中发挥降脂作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Novel therapeutic approach by culture filtrate of Cryptococcus neoformans var. gattii (CneF) in experimental immune complex glomerulonephritis

The present study was undertaken to determine the therapeutic effect of the culture filtrate of Cryptococcus neoformans var. gattii (CneF) in experimental immune complex glomerulonephritis. Bovine serum albumin (BSA) nephritis was induced in rats by a subcutaneous immunization and daily intravenous administration of BSA. CneF solution at three different doses (36, 54, and 90 mg/kg based on carbohydrate concentration) was administered intraperitoneally at regular 72-h intervals for 4 weeks. Onset of treatment was day 65, and urinary protein was measured at different intervals. Animals were euthanized on day 107. Serum and urine determinants were measured at the time of sacrifice and kidney specimens were examined. Results of this experiment showed that CneF therapy could significantly reduce the urinary protein excretion, blood urea nitrogen (BUN), plasma concentration of triglyceride, and increase the serum HDL cholesterol in treated rats vs. nontreated controls. Moreover, there was significant difference in glomerular changes between treated and nontreated groups. These observations show that the beneficial effect of CneF may be related to decreased number of glomerular leukocytes. Our findings suggest that treatment with CneF as a new antiinflammatory compound can reduce proteinuria, suppress the development of glomerular lesions, and exert lipid-lowering property in a rat model of immune complex glomerulonephritis.

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