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Protective effects and mechanisms of omega‐3 polyunsaturated fatty acid on intestinal injury and macrophage polarization in peritoneal dialysis rats

AIM: This study was conducted to investigate the chronic injury of peritoneal glucose injection on the peritoneum and intestine and the protective effects of omega‐3 polyunsaturated fatty acid (ω‐3PUFA) during peritoneal dialysis (PD). METHODS: Peritoneal dialysis animal models were established by i...

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Autores principales: Tang, Hanfen, Zhu, Xuping, Gong, Cai, Liu, Haiyang, Liu, Fuyou
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Australia, Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6790651/
https://www.ncbi.nlm.nih.gov/pubmed/30887626
http://dx.doi.org/10.1111/nep.13587
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author Tang, Hanfen
Zhu, Xuping
Gong, Cai
Liu, Haiyang
Liu, Fuyou
author_facet Tang, Hanfen
Zhu, Xuping
Gong, Cai
Liu, Haiyang
Liu, Fuyou
author_sort Tang, Hanfen
collection PubMed
description AIM: This study was conducted to investigate the chronic injury of peritoneal glucose injection on the peritoneum and intestine and the protective effects of omega‐3 polyunsaturated fatty acid (ω‐3PUFA) during peritoneal dialysis (PD). METHODS: Peritoneal dialysis animal models were established by intraperitoneal injection of 4.25% glucose for 28 days. Protein expression in ileum and peritoneum was measured by immunofloresence and immunohistochemistry. Protein expression in macrophages was measured by Western blot. Fibrosis was analyzed by Masson staining. RESULTS: Peritoneal dialysis significantly increased the structural injury and decreased junction‐related protein ZO‐1 and occludin expression in ileum, the expression of proteins relating to the activation of M2 (Erg2, IRF4), but not M1 (CD38, IRF5) macrophages. PD significantly increased the expression of TGF‐β1, VEGF and ALK5 protein in peritoneal tissues. PD significantly increased fibrosis (Masson staining) and the expression of fibroblast marker α‐SMA in peritoneal tissues. Injection of macrophage clean reagent and ω‐3PUFA significantly inhibited M2 activation, and decreased Masson staining, α‐SMA, TGF‐β1, VEGF and ALK5 protein expression in peritoneal tissues in PD treated rats. ω‐3PUFA injection significantly decreased PD‐induced injury in ileum and normalized the expression of ZO‐1 and occludin in the ileum of PD rats. CONCLUSION: Omega‐3 fatty acids can provide a protective role on PD‐induced peritoneal fibrosis and injury of the intestine.
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spelling pubmed-67906512019-10-18 Protective effects and mechanisms of omega‐3 polyunsaturated fatty acid on intestinal injury and macrophage polarization in peritoneal dialysis rats Tang, Hanfen Zhu, Xuping Gong, Cai Liu, Haiyang Liu, Fuyou Nephrology (Carlton) Original Article AIM: This study was conducted to investigate the chronic injury of peritoneal glucose injection on the peritoneum and intestine and the protective effects of omega‐3 polyunsaturated fatty acid (ω‐3PUFA) during peritoneal dialysis (PD). METHODS: Peritoneal dialysis animal models were established by intraperitoneal injection of 4.25% glucose for 28 days. Protein expression in ileum and peritoneum was measured by immunofloresence and immunohistochemistry. Protein expression in macrophages was measured by Western blot. Fibrosis was analyzed by Masson staining. RESULTS: Peritoneal dialysis significantly increased the structural injury and decreased junction‐related protein ZO‐1 and occludin expression in ileum, the expression of proteins relating to the activation of M2 (Erg2, IRF4), but not M1 (CD38, IRF5) macrophages. PD significantly increased the expression of TGF‐β1, VEGF and ALK5 protein in peritoneal tissues. PD significantly increased fibrosis (Masson staining) and the expression of fibroblast marker α‐SMA in peritoneal tissues. Injection of macrophage clean reagent and ω‐3PUFA significantly inhibited M2 activation, and decreased Masson staining, α‐SMA, TGF‐β1, VEGF and ALK5 protein expression in peritoneal tissues in PD treated rats. ω‐3PUFA injection significantly decreased PD‐induced injury in ileum and normalized the expression of ZO‐1 and occludin in the ileum of PD rats. CONCLUSION: Omega‐3 fatty acids can provide a protective role on PD‐induced peritoneal fibrosis and injury of the intestine. John Wiley & Sons Australia, Ltd 2019-04-04 2019-10 /pmc/articles/PMC6790651/ /pubmed/30887626 http://dx.doi.org/10.1111/nep.13587 Text en © 2019 The Authors Nephrology published by John Wiley & Sons Australia, Ltd on behalf of Asian Pacific Society of Nephrology This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Article
Tang, Hanfen
Zhu, Xuping
Gong, Cai
Liu, Haiyang
Liu, Fuyou
Protective effects and mechanisms of omega‐3 polyunsaturated fatty acid on intestinal injury and macrophage polarization in peritoneal dialysis rats
title Protective effects and mechanisms of omega‐3 polyunsaturated fatty acid on intestinal injury and macrophage polarization in peritoneal dialysis rats
title_full Protective effects and mechanisms of omega‐3 polyunsaturated fatty acid on intestinal injury and macrophage polarization in peritoneal dialysis rats
title_fullStr Protective effects and mechanisms of omega‐3 polyunsaturated fatty acid on intestinal injury and macrophage polarization in peritoneal dialysis rats
title_full_unstemmed Protective effects and mechanisms of omega‐3 polyunsaturated fatty acid on intestinal injury and macrophage polarization in peritoneal dialysis rats
title_short Protective effects and mechanisms of omega‐3 polyunsaturated fatty acid on intestinal injury and macrophage polarization in peritoneal dialysis rats
title_sort protective effects and mechanisms of omega‐3 polyunsaturated fatty acid on intestinal injury and macrophage polarization in peritoneal dialysis rats
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6790651/
https://www.ncbi.nlm.nih.gov/pubmed/30887626
http://dx.doi.org/10.1111/nep.13587
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