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炎症和脂代谢紊乱对大鼠肾脏损伤的协同作用。

Synergistic action of inflammation and lipid dysmetabolism on kidney damage in rats.

机构信息

a Chongqing Medical University , Chongqing , China.

b Department of Rheumatology and Immunology , The Second Affiliated Hospital of Chongqing Medical University , Chongqing , China.

出版信息

Ren Fail. 2018 Nov;40(1):175-182. doi: 10.1080/0886022X.2018.1450763.

Abstract

In kidney disease, inflammation and lipid dysmetabolism are often associated together, however, the effect and mechanism of inflammatory mediators and lipid dysmetabolism on kidney damage is still unclear. In this study, Wistar rats were randomized into four groups: normal diet + saline (Group N), high-fat diet (HF)+ saline (Group HF), normal diet + adriamycin (Group ADR), HF + adriamycin (Group ADR + HF). After 10 weeks of feeding, rats in each group were randomly sacrificed. We found that the protein content of urine in ADR and ADR + HF groups were significantly higher than that of group N and HF while the serum levels of total protein and albumin in the ADR and ADR + HF groups decreased correspondingly. The serum levels of triglyceride, total cholesterol and low-density lipoprotein in the HF, ADR and ADR + HF groups increased. In the treatment groups, mesangial proliferation, matrix accumulation, tubular vacuolization, inflammatory cell infiltration and fat deposition were detected. These pathological changes were the most serious in the ADR + HF group. The expression of tumor necrosis factor-α (TNF-α) and transforming growth factor-β1 (TGF-β1) were increased in each treatment group, especially in the ADR + HF group. Our results suggested that the inflammatory factors and abnormal lipid levels can activate the inflammatory response in kidney of the Wistar rats, and lead to a series of pathological changes in renal tissue, and inflammatory factors and lipid dysmetabolism can aggravate damage in the kidney.

摘要

在肾脏疾病中,炎症和脂质代谢紊乱通常同时存在,然而,炎症介质和脂质代谢紊乱对肾脏损伤的影响和机制尚不清楚。在这项研究中,Wistar 大鼠被随机分为四组:正常饮食+生理盐水(N 组)、高脂肪饮食+生理盐水(HF 组)、正常饮食+阿霉素(ADR 组)、高脂肪饮食+阿霉素(ADR+HF 组)。喂养 10 周后,每组大鼠随机处死。我们发现 ADR 和 ADR+HF 组大鼠的尿蛋白含量明显高于 N 组和 HF 组,而 ADR 和 ADR+HF 组大鼠的血清总蛋白和白蛋白水平相应下降。HF、ADR 和 ADR+HF 组大鼠的血清甘油三酯、总胆固醇和低密度脂蛋白水平升高。在治疗组中,观察到系膜增生、基质堆积、肾小管空泡化、炎性细胞浸润和脂肪沉积。ADR+HF 组的这些病理变化最为严重。TNF-α和 TGF-β1 的表达在每个治疗组中均增加,特别是在 ADR+HF 组中。我们的结果表明,炎症因子和异常的脂质水平可激活 Wistar 大鼠肾脏的炎症反应,导致肾脏组织发生一系列病理变化,炎症因子和脂质代谢紊乱可加重肾脏损伤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db09/6014339/6f0d3ffb9c5d/IRNF_A_1450763_F0001_B.jpg

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