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Metabolomics insights into chronic kidney disease and modulatory effect of rhubarb against tubulointerstitial fibrosis

Chronic kidney disease (CKD) is a major public health problem worldwide. Rhubarb has been shown to have nephroprotective and anti-fibrotic activities in patients with CKD. However, bioactive fractions and biochemical mechanism of anti-fibrotic properties of rhubarb remain unclear. Here we applied ul...

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Autores principales: Zhang, Zhi-Hao, Wei, Feng, Vaziri, Nosratola D., Cheng, Xian-Long, Bai, Xu, Lin, Rui-Chao, Zhao, Ying-Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4585987/
https://www.ncbi.nlm.nih.gov/pubmed/26412413
http://dx.doi.org/10.1038/srep14472
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author Zhang, Zhi-Hao
Wei, Feng
Vaziri, Nosratola D.
Cheng, Xian-Long
Bai, Xu
Lin, Rui-Chao
Zhao, Ying-Yong
author_facet Zhang, Zhi-Hao
Wei, Feng
Vaziri, Nosratola D.
Cheng, Xian-Long
Bai, Xu
Lin, Rui-Chao
Zhao, Ying-Yong
author_sort Zhang, Zhi-Hao
collection PubMed
description Chronic kidney disease (CKD) is a major public health problem worldwide. Rhubarb has been shown to have nephroprotective and anti-fibrotic activities in patients with CKD. However, bioactive fractions and biochemical mechanism of anti-fibrotic properties of rhubarb remain unclear. Here we applied ultra-performance liquid chromatography-quadrupole time-of-flight mass spectrometry together with univariate and multivariate statistical analyses to investigate the urinary metabolite profile in rats with adenine-induced CKD treated with the petroleum ether (PE)-, ethyl acetate (EA)- and n-butanol (BU)- extracts of rhubarb. Significant differences in renal function, kidney histopathology as well as metabolic profiles were observed between CKD and control rats. Changes in these parameters reflected characteristic phenotypes of CKD rats. We further identified a series of differential urinary metabolites for CKD rats, suggesting metabolic dysfunction in pathway of amino acid, purine, taurine, and choline metabolisms. Treatment with EA, BU and PE extracts of rhubarb improved renal function and histopathological abnormalities including interstitial fibrosis and inflammation, and either fully or partially reversed the abnormalities of the urinary metabolites. Among them, the nephroprotective effect of EA extract was stronger than BU and PE extracts. This work provides important mechanistic insights into the CKD and nephroprotective effects of different rhubarb extract against tubulo-interstitial fibrosis.
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spelling pubmed-45859872015-09-30 Metabolomics insights into chronic kidney disease and modulatory effect of rhubarb against tubulointerstitial fibrosis Zhang, Zhi-Hao Wei, Feng Vaziri, Nosratola D. Cheng, Xian-Long Bai, Xu Lin, Rui-Chao Zhao, Ying-Yong Sci Rep Article Chronic kidney disease (CKD) is a major public health problem worldwide. Rhubarb has been shown to have nephroprotective and anti-fibrotic activities in patients with CKD. However, bioactive fractions and biochemical mechanism of anti-fibrotic properties of rhubarb remain unclear. Here we applied ultra-performance liquid chromatography-quadrupole time-of-flight mass spectrometry together with univariate and multivariate statistical analyses to investigate the urinary metabolite profile in rats with adenine-induced CKD treated with the petroleum ether (PE)-, ethyl acetate (EA)- and n-butanol (BU)- extracts of rhubarb. Significant differences in renal function, kidney histopathology as well as metabolic profiles were observed between CKD and control rats. Changes in these parameters reflected characteristic phenotypes of CKD rats. We further identified a series of differential urinary metabolites for CKD rats, suggesting metabolic dysfunction in pathway of amino acid, purine, taurine, and choline metabolisms. Treatment with EA, BU and PE extracts of rhubarb improved renal function and histopathological abnormalities including interstitial fibrosis and inflammation, and either fully or partially reversed the abnormalities of the urinary metabolites. Among them, the nephroprotective effect of EA extract was stronger than BU and PE extracts. This work provides important mechanistic insights into the CKD and nephroprotective effects of different rhubarb extract against tubulo-interstitial fibrosis. Nature Publishing Group 2015-09-28 /pmc/articles/PMC4585987/ /pubmed/26412413 http://dx.doi.org/10.1038/srep14472 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Zhang, Zhi-Hao
Wei, Feng
Vaziri, Nosratola D.
Cheng, Xian-Long
Bai, Xu
Lin, Rui-Chao
Zhao, Ying-Yong
Metabolomics insights into chronic kidney disease and modulatory effect of rhubarb against tubulointerstitial fibrosis
title Metabolomics insights into chronic kidney disease and modulatory effect of rhubarb against tubulointerstitial fibrosis
title_full Metabolomics insights into chronic kidney disease and modulatory effect of rhubarb against tubulointerstitial fibrosis
title_fullStr Metabolomics insights into chronic kidney disease and modulatory effect of rhubarb against tubulointerstitial fibrosis
title_full_unstemmed Metabolomics insights into chronic kidney disease and modulatory effect of rhubarb against tubulointerstitial fibrosis
title_short Metabolomics insights into chronic kidney disease and modulatory effect of rhubarb against tubulointerstitial fibrosis
title_sort metabolomics insights into chronic kidney disease and modulatory effect of rhubarb against tubulointerstitial fibrosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4585987/
https://www.ncbi.nlm.nih.gov/pubmed/26412413
http://dx.doi.org/10.1038/srep14472
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