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首页> 外文期刊>Nephrology, dialysis, transplantation: official publication of the European Dialysis and Transplant Association - European Renal Association >Addition of oleic acid to delipidated bovine serum albumin aggravates renal damage in experimental protein-overload nephrosis.
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Addition of oleic acid to delipidated bovine serum albumin aggravates renal damage in experimental protein-overload nephrosis.

机译:在脱脂的牛血清白蛋白中添加油酸会加剧实验性蛋白超负荷肾病中的肾脏损害。

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摘要

BACKGROUND: Non-esterified fatty acids (NEFA) carried on albumin may have a causal role in the development of chronic proteinuria-induced nephropathy. To investigate whether NEFA aggravate renal structural damage, we studied the effects of NEFA addition to delipidated bovine serum albumin (BSA) in protein-overload nephropathy. METHODS: Three groups of Wistar rats received daily intraperitoneal injections (3 weeks) of either 1 g NEFA-free BSA (BSA-0), or NEFA-free BSA with three (BSA-3) or six (BSA-6) molecules oleic acid added per BSA molecule. An additional group received saline injections only (SAL). Renal damage was evaluated by immunohistochemistry and RT-PCR. RESULTS: Interstitial and glomerular alpha-smooth muscle actin (alpha-SMA, marker of myofibroblast transformation) expression were higher in BSA-3/6 than in saline-injected controls (P < 0.001). Glomerular macrophage influx and desmin (marker of glomerular epithelial cell damage) expression were higher in all BSA-injected rats than SAL (P < 0.001). Interstitial macrophage influx was elevated in BSA-0/3 (P < 0.05) and BSA-6 (P < 0.001) compared to SAL. Addition of six molecules of oleic acid to BSA revealed higher interstitial and glomerular alpha-SMA expression (P < 0.001), increased interstitial macrophage numbers (P < 0.001) and enhanced glomerular desmin expression (P < 0.05) compared to BSA-0. RT-PCR revealed higher glomerular alpha-SMA mRNA expression in BSA-3/6 than SAL (P < 0.001 and 0.05, respectively), interstitial alpha-SMA mRNA was elevated in BSA-6 (P < 0.05). Interstitial TGF-beta1 mRNA expression was significantly higher in BSA-3 than SAL (P < 0.05). CONCLUSIONS: These data show that addition of oleic acid to NEFA-free BSA aggravates renal damage, suggesting a role for NEFA in the pathogenesis of proteinuric nephropathies.
机译:背景:白蛋白上携带的非酯化脂肪酸(NEFA)可能在慢性蛋白尿引起的肾病的发展中起因果作用。为了研究NEFA是否加重了肾脏的结构损伤,我们研究了NEFA加脂蛋白牛血清白蛋白(BSA)在蛋白质超负荷肾病中的作用。方法:三组Wistar大鼠每天接受腹膜内注射(3周),每次1 g无NEFA的BSA(BSA-0)或无NEFA的BSA,其中三个(BSA-3)或六个(BSA-6)分子油性每个BSA分子添加的酸。另外一组仅接受盐水注射(SAL)。通过免疫组织化学和RT-PCR评估肾损伤。结果:BSA-3 / 6中的间质和肾小球α-平滑肌肌动蛋白(α-SMA,成肌纤维细胞转化的标志物)的表达高于注射生理盐水的对照组(P <0.001)。在所有注射BSA的大鼠中,肾小球巨噬细胞的内流和结蛋白(肾小球上皮细胞损伤的标志)的表达均高于SAL(P <0.001)。与SAL相比,BSA-0 / 3(P <0.05)和BSA-6(P <0.001)的间质巨噬细胞内流增加。与BSA-0相比,向BSA中添加6个油酸分子显示出较高的间质和肾小球α-SMA表达(P <0.001),增加的间质巨噬细胞数目(P <0.001)和增强的肾小球结蛋白表达(P <0.05)。 RT-PCR显示BSA-3 / 6中的肾小球α-SMAmRNA表达高于SAL(分别为P <0.001和0.05),间质性α-SMAmRNA在BSA-6中升高(P <0.05)。在BSA-3中,间质TGF-beta1 mRNA表达显着高于SAL(P <0.05)。结论:这些数据表明,向不含NEFA的BSA中添加油酸会加重肾脏损害,提示NEFA在蛋白尿性肾病的发病机理中具有重要作用。

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