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机构地区:[1]江苏食品药品职业技术学院药学院,江苏淮安223003
出 处:《中国病理生理杂志》2016年第10期1887-1891,共5页Chinese Journal of Pathophysiology
摘 要:目的:观察依维莫司对大鼠实验性Ig A肾病的作用并初步探讨其机制。方法:建立实验性Ig A肾病大鼠模型,实验共分为正常对照(control)组、模型组(Ig A组)和依维莫司给药组;测定给药后各组大鼠尿红细胞、尿蛋白和尿N-乙酰-β-D-氨基葡萄糖苷酶(NAG)的含量;免疫荧光染色检测肾组织中Ig A沉淀情况;Western blot法检测髓样分化因子88(My D88)、TLR4、NF-κB、IL-4和IL-13的蛋白表达水平;实时荧光定量PCR检测IL-4与IL-13的mRNA表达水平。结果:依维莫司能够抑制实验性Ig A肾病大鼠尿红细胞、尿蛋白和尿NAG含量的升高,抑制My D88、TLR4、NF-κB和IL-4和IL-13蛋白表达水平的上调,以及抑制IL-4和IL-13 mRNA表达水平的上调。结论:依维莫司能降低Ig A肾病大鼠尿红细胞、尿蛋白和尿NAG含量,其作用可能与其调节My D88、TLR4、NF-κB、IL-4与IL-13的表达有关。AIM:To investigate the effects of everolimus on the experimental IgA nephropathy in rats and its possible mechanisms .METHODS:The rat model of experimental IgA nephropathy was established .The rats were randomly divided into control group , IgA group and everolimus treatment group .After the corresponding treatments were given, urinary red blood cells , protein and N-acetyl-β-D-glucosaminidase ( NAG) were examined .Immunofluorescence staining was used to analyze the level of IgA precipitation in the renal tissues .Additionally, the protein expression of myeloid differentiation factor 88 (MyD88), TLR4, NF-κB, IL-4 and IL-13 was determined by Western blot.The mRNA levels of IL-4 and IL-13 were detected by qPCR .RESULTS:Everolimus significantly inhibited the increases in the urinary levels of red blood cells, protein and NAG in experimental IgA nephropathy rats .Furthermore, IgA nephropathy-induced increases in the protein expression of MyD88, TLR4, NF-κB, IL-4 and IL-13 were attenuated after everolimus treatment .Similar results were obtained in the mRNA levels of IL-4 and IL-13 by qPCR detection .CONCLUSION: Everolimus improves the impairments of renal function in experimental IgA nephropathy rats as evidenced by decreasing urinary red blood cells , protein and NAG, which may be related to the inhibition of MyD 88, TLR4, NF-κB, IL-4 and IL-13 expression.
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