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Phenotypic characterization of nanshi oral liquid alters metabolic signatures during disease prevention
This paper was designed to investigate the phenotypic characterization of Nanshi Oral Liquid (NOL) alters metabolic signatures of the ‘Kidney Yang Deficiency syndrome’ (KYDS). Urine metabolites were profiled by UPLC-ESI-Q-TOF-HDMS. The significantly changed metabolites such as xanthurenic acid, 4,8-...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4726315/ https://www.ncbi.nlm.nih.gov/pubmed/26785698 http://dx.doi.org/10.1038/srep19333 |
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author | Zhang, Aihua Liu, Qi Zhao, Hongwei Zhou, Xiaohang Sun, Hui Nan, Yang Zou, Shiyu Ma, Chung Wah Wang, Xijun |
author_facet | Zhang, Aihua Liu, Qi Zhao, Hongwei Zhou, Xiaohang Sun, Hui Nan, Yang Zou, Shiyu Ma, Chung Wah Wang, Xijun |
author_sort | Zhang, Aihua |
collection | PubMed |
description | This paper was designed to investigate the phenotypic characterization of Nanshi Oral Liquid (NOL) alters metabolic signatures of the ‘Kidney Yang Deficiency syndrome’ (KYDS). Urine metabolites were profiled by UPLC-ESI-Q-TOF-HDMS. The significantly changed metabolites such as xanthurenic acid, 4,8-dihydroxyquinoline, 3-methyldioxyindole, 4,6-dihydroxyquinoline, kynurenic acid, hippuric acid, taurine, tyramine, and 3-metanephrine, had been identified, and were related to the disturbance in tyrosine metabolism, steroid hormone biosynthesis, taurine and hypotaurine metabolism, tryptophan metabolism, phenylalanine metabolism and lysine degradation, which were helpful to further understanding the KYDS and intervention mechanism of NOL. The biochemical result showed that NOL can alleviate the kidney impairment induced by KYDS. Metabolomics results indicated the significantly changed metabolites were found to be reasonable in explaining the action mechanism of NOL. Interestingly, the effectiveness of NOL against KYDS was proved using the established metabolomics method and regulated the biomarkers as well as adjusted the metabolic disorder pathways. NOL had potentially pharmacological effect through regulating multiple perturbed pathways to normal state. This work showed that the metabolomics method was a powerful approach for studying the phenotypic characterization of disease’s syndrome during disease prevention and its intervention mechanism. |
format | Online Article Text |
id | pubmed-4726315 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47263152016-01-27 Phenotypic characterization of nanshi oral liquid alters metabolic signatures during disease prevention Zhang, Aihua Liu, Qi Zhao, Hongwei Zhou, Xiaohang Sun, Hui Nan, Yang Zou, Shiyu Ma, Chung Wah Wang, Xijun Sci Rep Article This paper was designed to investigate the phenotypic characterization of Nanshi Oral Liquid (NOL) alters metabolic signatures of the ‘Kidney Yang Deficiency syndrome’ (KYDS). Urine metabolites were profiled by UPLC-ESI-Q-TOF-HDMS. The significantly changed metabolites such as xanthurenic acid, 4,8-dihydroxyquinoline, 3-methyldioxyindole, 4,6-dihydroxyquinoline, kynurenic acid, hippuric acid, taurine, tyramine, and 3-metanephrine, had been identified, and were related to the disturbance in tyrosine metabolism, steroid hormone biosynthesis, taurine and hypotaurine metabolism, tryptophan metabolism, phenylalanine metabolism and lysine degradation, which were helpful to further understanding the KYDS and intervention mechanism of NOL. The biochemical result showed that NOL can alleviate the kidney impairment induced by KYDS. Metabolomics results indicated the significantly changed metabolites were found to be reasonable in explaining the action mechanism of NOL. Interestingly, the effectiveness of NOL against KYDS was proved using the established metabolomics method and regulated the biomarkers as well as adjusted the metabolic disorder pathways. NOL had potentially pharmacological effect through regulating multiple perturbed pathways to normal state. This work showed that the metabolomics method was a powerful approach for studying the phenotypic characterization of disease’s syndrome during disease prevention and its intervention mechanism. Nature Publishing Group 2016-01-20 /pmc/articles/PMC4726315/ /pubmed/26785698 http://dx.doi.org/10.1038/srep19333 Text en Copyright © 2016, 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, Aihua Liu, Qi Zhao, Hongwei Zhou, Xiaohang Sun, Hui Nan, Yang Zou, Shiyu Ma, Chung Wah Wang, Xijun Phenotypic characterization of nanshi oral liquid alters metabolic signatures during disease prevention |
title | Phenotypic characterization of nanshi oral liquid alters metabolic signatures during disease prevention |
title_full | Phenotypic characterization of nanshi oral liquid alters metabolic signatures during disease prevention |
title_fullStr | Phenotypic characterization of nanshi oral liquid alters metabolic signatures during disease prevention |
title_full_unstemmed | Phenotypic characterization of nanshi oral liquid alters metabolic signatures during disease prevention |
title_short | Phenotypic characterization of nanshi oral liquid alters metabolic signatures during disease prevention |
title_sort | phenotypic characterization of nanshi oral liquid alters metabolic signatures during disease prevention |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4726315/ https://www.ncbi.nlm.nih.gov/pubmed/26785698 http://dx.doi.org/10.1038/srep19333 |
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