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Resistant starch slows the progression of CKD in the 5/6 nephrectomy mouse model
BACKGROUND: Resistant Starch (RS) improves CKD outcomes. In this report, we study how RS modulates host‐microbiome interactions in CKD by measuring changes in the abundance of proteins and bacteria in the gut. In addition, we demonstrate RS‐mediated reduction in CKD‐induced kidney damage. METHODS: E...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7547583/ https://www.ncbi.nlm.nih.gov/pubmed/33038060 http://dx.doi.org/10.14814/phy2.14610 |
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author | Karaduta, Oleg Glazko, Galina Dvanajscak, Zeljko Arthur, John Mackintosh, Samuel Orr, Lisa Rahmatallah, Yasir Yeruva, Laxmi Tackett, Alan Zybailov, Boris |
author_facet | Karaduta, Oleg Glazko, Galina Dvanajscak, Zeljko Arthur, John Mackintosh, Samuel Orr, Lisa Rahmatallah, Yasir Yeruva, Laxmi Tackett, Alan Zybailov, Boris |
author_sort | Karaduta, Oleg |
collection | PubMed |
description | BACKGROUND: Resistant Starch (RS) improves CKD outcomes. In this report, we study how RS modulates host‐microbiome interactions in CKD by measuring changes in the abundance of proteins and bacteria in the gut. In addition, we demonstrate RS‐mediated reduction in CKD‐induced kidney damage. METHODS: Eight mice underwent 5/6 nephrectomy to induce CKD and eight served as healthy controls. CKD and Healthy (H) groups were further split into those receiving RS (CKDRS, n = 4; HRS, n = 4) and those on normal diet (CKD, n = 4, H, n = 4). Kidney injury was evaluated by measuring BUN/creatinine and by histopathological evaluation. Cecal contents were analyzed using mass spectrometry‐based metaproteomics and de novo sequencing using PEAKS. All the data were analyzed using R/Bioconductor packages. RESULTS: The 5/6 nephrectomy compromised kidney function as seen by an increase in BUN/creatinine compared to healthy groups. Histopathology of kidney sections showed reduced tubulointerstitial injury in the CKDRS versus CKD group; while no significant difference in BUN/creatinine was observed between the two CKD groups. Identified proteins point toward a higher population of butyrate‐producing bacteria, reduced abundance of mucin‐degrading bacteria in the RS fed groups, and to the downregulation of indole metabolism in CKD groups. CONCLUSION: RS slows the progression of chronic kidney disease. Resistant starch supplementation leads to active bacterial proliferation and the reduction of harmful bacterial metabolites. |
format | Online Article Text |
id | pubmed-7547583 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75475832020-10-16 Resistant starch slows the progression of CKD in the 5/6 nephrectomy mouse model Karaduta, Oleg Glazko, Galina Dvanajscak, Zeljko Arthur, John Mackintosh, Samuel Orr, Lisa Rahmatallah, Yasir Yeruva, Laxmi Tackett, Alan Zybailov, Boris Physiol Rep Original Research BACKGROUND: Resistant Starch (RS) improves CKD outcomes. In this report, we study how RS modulates host‐microbiome interactions in CKD by measuring changes in the abundance of proteins and bacteria in the gut. In addition, we demonstrate RS‐mediated reduction in CKD‐induced kidney damage. METHODS: Eight mice underwent 5/6 nephrectomy to induce CKD and eight served as healthy controls. CKD and Healthy (H) groups were further split into those receiving RS (CKDRS, n = 4; HRS, n = 4) and those on normal diet (CKD, n = 4, H, n = 4). Kidney injury was evaluated by measuring BUN/creatinine and by histopathological evaluation. Cecal contents were analyzed using mass spectrometry‐based metaproteomics and de novo sequencing using PEAKS. All the data were analyzed using R/Bioconductor packages. RESULTS: The 5/6 nephrectomy compromised kidney function as seen by an increase in BUN/creatinine compared to healthy groups. Histopathology of kidney sections showed reduced tubulointerstitial injury in the CKDRS versus CKD group; while no significant difference in BUN/creatinine was observed between the two CKD groups. Identified proteins point toward a higher population of butyrate‐producing bacteria, reduced abundance of mucin‐degrading bacteria in the RS fed groups, and to the downregulation of indole metabolism in CKD groups. CONCLUSION: RS slows the progression of chronic kidney disease. Resistant starch supplementation leads to active bacterial proliferation and the reduction of harmful bacterial metabolites. John Wiley and Sons Inc. 2020-10-10 /pmc/articles/PMC7547583/ /pubmed/33038060 http://dx.doi.org/10.14814/phy2.14610 Text en © 2020 The Authors. Physiological Reports published by Wiley Periodicals LLC on behalf of The Physiological Society and the American Physiological Society This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Karaduta, Oleg Glazko, Galina Dvanajscak, Zeljko Arthur, John Mackintosh, Samuel Orr, Lisa Rahmatallah, Yasir Yeruva, Laxmi Tackett, Alan Zybailov, Boris Resistant starch slows the progression of CKD in the 5/6 nephrectomy mouse model |
title | Resistant starch slows the progression of CKD in the 5/6 nephrectomy mouse model |
title_full | Resistant starch slows the progression of CKD in the 5/6 nephrectomy mouse model |
title_fullStr | Resistant starch slows the progression of CKD in the 5/6 nephrectomy mouse model |
title_full_unstemmed | Resistant starch slows the progression of CKD in the 5/6 nephrectomy mouse model |
title_short | Resistant starch slows the progression of CKD in the 5/6 nephrectomy mouse model |
title_sort | resistant starch slows the progression of ckd in the 5/6 nephrectomy mouse model |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7547583/ https://www.ncbi.nlm.nih.gov/pubmed/33038060 http://dx.doi.org/10.14814/phy2.14610 |
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