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

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), h...

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Autores principales: Wang, Zhongjie, Huang, Wenhan, Li, Hui, Tang, Lin, Sun, Hang, Liu, Qi, Zhang, Ling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6014339/
https://www.ncbi.nlm.nih.gov/pubmed/29569980
http://dx.doi.org/10.1080/0886022X.2018.1450763
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author Wang, Zhongjie
Huang, Wenhan
Li, Hui
Tang, Lin
Sun, Hang
Liu, Qi
Zhang, Ling
author_facet Wang, Zhongjie
Huang, Wenhan
Li, Hui
Tang, Lin
Sun, Hang
Liu, Qi
Zhang, Ling
author_sort Wang, Zhongjie
collection PubMed
description 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.
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spelling pubmed-60143392018-06-28 Synergistic action of inflammation and lipid dysmetabolism on kidney damage in rats Wang, Zhongjie Huang, Wenhan Li, Hui Tang, Lin Sun, Hang Liu, Qi Zhang, Ling Ren Fail Laboratory Study 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. Taylor & Francis 2018-03-23 /pmc/articles/PMC6014339/ /pubmed/29569980 http://dx.doi.org/10.1080/0886022X.2018.1450763 Text en © 2018 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Laboratory Study
Wang, Zhongjie
Huang, Wenhan
Li, Hui
Tang, Lin
Sun, Hang
Liu, Qi
Zhang, Ling
Synergistic action of inflammation and lipid dysmetabolism on kidney damage in rats
title Synergistic action of inflammation and lipid dysmetabolism on kidney damage in rats
title_full Synergistic action of inflammation and lipid dysmetabolism on kidney damage in rats
title_fullStr Synergistic action of inflammation and lipid dysmetabolism on kidney damage in rats
title_full_unstemmed Synergistic action of inflammation and lipid dysmetabolism on kidney damage in rats
title_short Synergistic action of inflammation and lipid dysmetabolism on kidney damage in rats
title_sort synergistic action of inflammation and lipid dysmetabolism on kidney damage in rats
topic Laboratory Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6014339/
https://www.ncbi.nlm.nih.gov/pubmed/29569980
http://dx.doi.org/10.1080/0886022X.2018.1450763
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