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Sanziguben polysaccharides inhibit diabetic nephropathy through NF-κB-mediated anti-inflammation
BACKGROUND: Sanziguben polysaccharides (SZP) are large amounts of classical Chinese medicines from Sanziguben (SZGB). Moreover, SZGB is a widely applied compound prescription for diabetic nephropathy (DN) treatment, but the role is still unclear. This study initially explores the mechanism of SZP in...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8425148/ https://www.ncbi.nlm.nih.gov/pubmed/34493288 http://dx.doi.org/10.1186/s12986-021-00601-z |
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author | Zhou, Kang Zhang, Jianing Liu, Chang Ou, Lijuan Wang, Fan Yu, Yang Wang, Yumei Bai, Shasha |
author_facet | Zhou, Kang Zhang, Jianing Liu, Chang Ou, Lijuan Wang, Fan Yu, Yang Wang, Yumei Bai, Shasha |
author_sort | Zhou, Kang |
collection | PubMed |
description | BACKGROUND: Sanziguben polysaccharides (SZP) are large amounts of classical Chinese medicines from Sanziguben (SZGB). Moreover, SZGB is a widely applied compound prescription for diabetic nephropathy (DN) treatment, but the role is still unclear. This study initially explores the mechanism of SZP in the treatment of DN. METHODS: The high-fat diet plus streptozotocin injections were used to replicate the DN models in male C57BL/6 mice. DN mice were divided into five groups: DN mice, DN mice treated with SZP(1.01 or 2.02 g/kg), DN mice treated with SZGB decoction(4.7 g/kg), and DN mice treated with metformin (300 mg/kg). HG and LPS plus TNFα stimulated human tubule epithelial (HK-2) cells to establish an in vitro model and treated with SZP (100 or 200 μg/mL). RESULTS: SZP was found to comprise sugar, protein, and uronic acid. Furthermore, SZP alleviated the progression of inflammation in vivo and in vitro by inhibiting the expression of NF-κB. CONCLUSIONS: NF-κB plays a critical role in the development of DN induced by STZ and HG. Furthermore, SZP can attenuate the NF-κB‐mediated progression of diabetic nephropathy, improve DN through anti-inflammation. |
format | Online Article Text |
id | pubmed-8425148 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-84251482021-09-10 Sanziguben polysaccharides inhibit diabetic nephropathy through NF-κB-mediated anti-inflammation Zhou, Kang Zhang, Jianing Liu, Chang Ou, Lijuan Wang, Fan Yu, Yang Wang, Yumei Bai, Shasha Nutr Metab (Lond) Research BACKGROUND: Sanziguben polysaccharides (SZP) are large amounts of classical Chinese medicines from Sanziguben (SZGB). Moreover, SZGB is a widely applied compound prescription for diabetic nephropathy (DN) treatment, but the role is still unclear. This study initially explores the mechanism of SZP in the treatment of DN. METHODS: The high-fat diet plus streptozotocin injections were used to replicate the DN models in male C57BL/6 mice. DN mice were divided into five groups: DN mice, DN mice treated with SZP(1.01 or 2.02 g/kg), DN mice treated with SZGB decoction(4.7 g/kg), and DN mice treated with metformin (300 mg/kg). HG and LPS plus TNFα stimulated human tubule epithelial (HK-2) cells to establish an in vitro model and treated with SZP (100 or 200 μg/mL). RESULTS: SZP was found to comprise sugar, protein, and uronic acid. Furthermore, SZP alleviated the progression of inflammation in vivo and in vitro by inhibiting the expression of NF-κB. CONCLUSIONS: NF-κB plays a critical role in the development of DN induced by STZ and HG. Furthermore, SZP can attenuate the NF-κB‐mediated progression of diabetic nephropathy, improve DN through anti-inflammation. BioMed Central 2021-09-07 /pmc/articles/PMC8425148/ /pubmed/34493288 http://dx.doi.org/10.1186/s12986-021-00601-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Zhou, Kang Zhang, Jianing Liu, Chang Ou, Lijuan Wang, Fan Yu, Yang Wang, Yumei Bai, Shasha Sanziguben polysaccharides inhibit diabetic nephropathy through NF-κB-mediated anti-inflammation |
title | Sanziguben polysaccharides inhibit diabetic nephropathy through NF-κB-mediated anti-inflammation |
title_full | Sanziguben polysaccharides inhibit diabetic nephropathy through NF-κB-mediated anti-inflammation |
title_fullStr | Sanziguben polysaccharides inhibit diabetic nephropathy through NF-κB-mediated anti-inflammation |
title_full_unstemmed | Sanziguben polysaccharides inhibit diabetic nephropathy through NF-κB-mediated anti-inflammation |
title_short | Sanziguben polysaccharides inhibit diabetic nephropathy through NF-κB-mediated anti-inflammation |
title_sort | sanziguben polysaccharides inhibit diabetic nephropathy through nf-κb-mediated anti-inflammation |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8425148/ https://www.ncbi.nlm.nih.gov/pubmed/34493288 http://dx.doi.org/10.1186/s12986-021-00601-z |
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