首页> 美国卫生研究院文献>The Journal of Clinical Investigation >Inhibitory role of dietary protein restriction on the development and expression of immune-mediated antitubular basement membrane-induced tubulointerstitial nephritis in rats.
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Inhibitory role of dietary protein restriction on the development and expression of immune-mediated antitubular basement membrane-induced tubulointerstitial nephritis in rats.

机译:饮食中蛋白质的限制对免疫介导的抗肾小管基底膜诱发的肾小管间质性肾炎的发展和表达的抑制作用。

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摘要

The protective effect of dietary protein restriction on the development and expression of immune-mediated interstitial nephritis was evaluated in Brown Norway rats with anti-tubular basement membrane disease. In the first series of experiments, pair-fed rats received low protein (LP) (3% casein) or normal protein (NP) (27% casein), normocaloric diets. After 6 wk, each group was immunized with renal tubular antigen in adjuvant to produce anti-tubular basement membrane antibody (alpha TBM-Ab) and tubulointerstitial nephritis. The kidneys harvested from NP rats after four more weeks on the diet had histologically more severe interstitial disease than the LP rats (histologic severity; NP = 3.1 +/- 0.2 vs. LP = 1.1 +/- 0.3; P less than 0.001), and serum creatinine values were concordantly different (NP = 1.34 +/- 0.02 vs. LP = 0.82 +/- 0.03). Titers of alpha TBM-Ab were similar in both groups, while the T cell-mediated immune response, as measured by delayed-type hypersensitivity (DTH), was nonspecifically impaired in LP rats when compared with the NP group. Admixture cotransfers of LP plus NP cells failed to demonstrate active suppression as an explanation for the depressed DTH in LP rats. The therapeutic role of dietary protein restriction was also examined in rats with established alpha TBM disease. In these experiments, rats were first immunized and fed NP diets for 4 wk (histologic severity = 3.0 +/- 0.2; creatinine = 1.78 +/- 0.02), and then were divided into two groups and followed for six more weeks on either LP or NP diets. LP rats, under these conditions, developed less disease than those fed NP diet (histologic severity; NP = 3.2 +/- 0.3 vs. LP = 1.4 +/- 0.2; P less than 0.001), and serum creatinine values were concordantly different (NP = 1.92 +/- 0.05 vs. LP = 0.97 +/- 0.02). Again, the titers of alpha TBM-Ab in both LP and NP groups were similar. These data collectively suggest that LP diet has a protective effect both on the development and extent of tubulointerstitial nephritis that is perhaps, in part, related to the selective abrogation of effector T cell immunity.
机译:在患有抗肾小管基底膜疾病的褐挪威大鼠中,评估了饮食蛋白限制对免疫介导的间质性肾炎的发生和表达的保护作用。在第一批实验中,成对喂养的大鼠接受低热量饮食,摄入低蛋白(LP)(3%酪蛋白)或正常蛋白(NP)(27%酪蛋白)。 6周后,每组均用佐剂中的肾小管抗原免疫,以产生抗小管基底膜抗体(αTBM-Ab)和肾小管间质性肾炎。在饮食上再过四周后,从NP大鼠中收获的肾脏在组织学上比LP大鼠更严重的间质疾病(组织学严重度; NP = 3.1 +/- 0.2与LP = 1.1 +/- 0.3; P小于0.001),和血清肌酐值一致地不同(NP = 1.34 +/- 0.02 vs. LP = 0.82 +/- 0.03)。在两组中,αTBM-Ab的滴度相似,而与NP组相比,通过延迟型超敏反应(DTH)测得的T细胞介导的免疫反应在LP大鼠中无特异性受损。 LP加NP细胞的混合物共转移未能显示出主动抑制作用,这可解释LP大鼠DTH降低。饮食蛋白限制的治疗作用也已在患有既定的αTBM疾病的大鼠中进行了检查。在这些实验中,首先对大鼠进行免疫接种,并以NP日粮喂养4周(组织学严重度= 3.0 +/- 0.2;肌酐= 1.78 +/- 0.02),然后分为两组,然后在任一LP上再治疗6周或NP饮食。在这些条件下,LP大鼠的疾病发病率低于NP饮食(组织学严重程度; NP = 3.2 +/- 0.3 vs. LP = 1.4 +/- 0.2; P小于0.001),并且血清肌酐值也存在差异( NP = 1.92 +/- 0.05与LP = 0.97 +/- 0.02)。同样,LP和NP组中的αTBM-Ab的效价相似。这些数据共同表明,LP饮食对肾小管间质性肾炎的发展和程度均具有保护作用,这可能部分与选择性消除效应T细胞免疫有关。

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