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Baicalein decreases uric acid and prevents hyperuricemic nephropathy in mice

Baicalein, a natural flavonoid, is structurally advantageous for binding to xanthine oxidoreductase. In our study, molecular docking analysis and Surface Plasmon Resonance revealed a direct interaction between baicalein and xanthine oxidoreductase. Moreover, 50 mg/kg/d baicalein treatment significan...

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Autores principales: Meng, Xiaolu, Mao, Zhuo, Li, Xin, Zhong, Dandan, Li, Min, Jia, Yingli, Wei, Jing, Yang, Baoxue, Zhou, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5522264/
https://www.ncbi.nlm.nih.gov/pubmed/28445133
http://dx.doi.org/10.18632/oncotarget.16928
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author Meng, Xiaolu
Mao, Zhuo
Li, Xin
Zhong, Dandan
Li, Min
Jia, Yingli
Wei, Jing
Yang, Baoxue
Zhou, Hong
author_facet Meng, Xiaolu
Mao, Zhuo
Li, Xin
Zhong, Dandan
Li, Min
Jia, Yingli
Wei, Jing
Yang, Baoxue
Zhou, Hong
author_sort Meng, Xiaolu
collection PubMed
description Baicalein, a natural flavonoid, is structurally advantageous for binding to xanthine oxidoreductase. In our study, molecular docking analysis and Surface Plasmon Resonance revealed a direct interaction between baicalein and xanthine oxidoreductase. Moreover, 50 mg/kg/d baicalein treatment significantly suppressed the viability of xanthine oxidoreductase in hyperuricemia mouse model. The data showed that baicalein remarkably prevented renal dysfunction, ameliorated kidney fibrosis, alleviated epithelial-mesenchymal transition and oxidative stress in hyperuricemia mice. Thus, we concluded that baicalein executed a kidney-protection action in hyperuricemia and therefore may be used as a therapeutic alternative for hyperuricemic nephropathy.
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spelling pubmed-55222642017-08-21 Baicalein decreases uric acid and prevents hyperuricemic nephropathy in mice Meng, Xiaolu Mao, Zhuo Li, Xin Zhong, Dandan Li, Min Jia, Yingli Wei, Jing Yang, Baoxue Zhou, Hong Oncotarget Research Paper Baicalein, a natural flavonoid, is structurally advantageous for binding to xanthine oxidoreductase. In our study, molecular docking analysis and Surface Plasmon Resonance revealed a direct interaction between baicalein and xanthine oxidoreductase. Moreover, 50 mg/kg/d baicalein treatment significantly suppressed the viability of xanthine oxidoreductase in hyperuricemia mouse model. The data showed that baicalein remarkably prevented renal dysfunction, ameliorated kidney fibrosis, alleviated epithelial-mesenchymal transition and oxidative stress in hyperuricemia mice. Thus, we concluded that baicalein executed a kidney-protection action in hyperuricemia and therefore may be used as a therapeutic alternative for hyperuricemic nephropathy. Impact Journals LLC 2017-04-07 /pmc/articles/PMC5522264/ /pubmed/28445133 http://dx.doi.org/10.18632/oncotarget.16928 Text en Copyright: © 2017 Meng et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (http://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Meng, Xiaolu
Mao, Zhuo
Li, Xin
Zhong, Dandan
Li, Min
Jia, Yingli
Wei, Jing
Yang, Baoxue
Zhou, Hong
Baicalein decreases uric acid and prevents hyperuricemic nephropathy in mice
title Baicalein decreases uric acid and prevents hyperuricemic nephropathy in mice
title_full Baicalein decreases uric acid and prevents hyperuricemic nephropathy in mice
title_fullStr Baicalein decreases uric acid and prevents hyperuricemic nephropathy in mice
title_full_unstemmed Baicalein decreases uric acid and prevents hyperuricemic nephropathy in mice
title_short Baicalein decreases uric acid and prevents hyperuricemic nephropathy in mice
title_sort baicalein decreases uric acid and prevents hyperuricemic nephropathy in mice
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5522264/
https://www.ncbi.nlm.nih.gov/pubmed/28445133
http://dx.doi.org/10.18632/oncotarget.16928
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