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Salvianolic acid A as a multifunctional agent ameliorates doxorubicin-induced nephropathy in rats
Nephrotic syndrome (NS) is still a therapeutic challenge. To date there is no ideal treatment. Evidence suggest that multidrug therapy has more effect than monotherapy in amelioration of renal injury. Salvianolic acid A (SAA) is the major active component of Salviae Miltiorrhizae Bunge. Previous stu...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4508635/ https://www.ncbi.nlm.nih.gov/pubmed/26194431 http://dx.doi.org/10.1038/srep12273 |
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author | Fan, Hua-Ying Yang, Ming-Yan Qi, Dong Zhang, Zuo-Kai Zhu, Lin Shang-Guan, Xiu-Xin Liu, Ke Xu, Hui Che, Xin |
author_facet | Fan, Hua-Ying Yang, Ming-Yan Qi, Dong Zhang, Zuo-Kai Zhu, Lin Shang-Guan, Xiu-Xin Liu, Ke Xu, Hui Che, Xin |
author_sort | Fan, Hua-Ying |
collection | PubMed |
description | Nephrotic syndrome (NS) is still a therapeutic challenge. To date there is no ideal treatment. Evidence suggest that multidrug therapy has more effect than monotherapy in amelioration of renal injury. Salvianolic acid A (SAA) is the major active component of Salviae Miltiorrhizae Bunge. Previous studies have demonstrated that SAA is a multi-target agent and has various pharmacological activities. The pleiotropic properties of SAA predict its potential in the treatment of NS. The study investigated the effect of SAA on doxorubicin-induced nephropathy. The kidney function related-biochemical changes, hemorheological parameters and oxidative stress status were determined, and histological examination using light and transmission electron microcopies and western blot analysis were also performed. Results revealed that treatment with SAA alleviated histological damages, relieved proteinuria, hypoalbuminemia and hyperlipidemia, reduced oxidative stress, as well as improving hemorheology. Furthermore, SAA restored podocin expression, down-regulated the expression of NF-κB p65 and p-IκBα while up-regulating IκBα protein expression. Overall, as a multifunctional agent, SAA has a favorable renoprotection in doxorubicin-induced nephropathy. The anti-inflammation, antioxidant, amelioration of podocyte injury, improvement of hemorheology and hypolipidemic properties may constituent an important part of its therapeutic effects. All these indicate that SAA is likely to be a promising agent for NS. |
format | Online Article Text |
id | pubmed-4508635 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-45086352015-07-28 Salvianolic acid A as a multifunctional agent ameliorates doxorubicin-induced nephropathy in rats Fan, Hua-Ying Yang, Ming-Yan Qi, Dong Zhang, Zuo-Kai Zhu, Lin Shang-Guan, Xiu-Xin Liu, Ke Xu, Hui Che, Xin Sci Rep Article Nephrotic syndrome (NS) is still a therapeutic challenge. To date there is no ideal treatment. Evidence suggest that multidrug therapy has more effect than monotherapy in amelioration of renal injury. Salvianolic acid A (SAA) is the major active component of Salviae Miltiorrhizae Bunge. Previous studies have demonstrated that SAA is a multi-target agent and has various pharmacological activities. The pleiotropic properties of SAA predict its potential in the treatment of NS. The study investigated the effect of SAA on doxorubicin-induced nephropathy. The kidney function related-biochemical changes, hemorheological parameters and oxidative stress status were determined, and histological examination using light and transmission electron microcopies and western blot analysis were also performed. Results revealed that treatment with SAA alleviated histological damages, relieved proteinuria, hypoalbuminemia and hyperlipidemia, reduced oxidative stress, as well as improving hemorheology. Furthermore, SAA restored podocin expression, down-regulated the expression of NF-κB p65 and p-IκBα while up-regulating IκBα protein expression. Overall, as a multifunctional agent, SAA has a favorable renoprotection in doxorubicin-induced nephropathy. The anti-inflammation, antioxidant, amelioration of podocyte injury, improvement of hemorheology and hypolipidemic properties may constituent an important part of its therapeutic effects. All these indicate that SAA is likely to be a promising agent for NS. Nature Publishing Group 2015-07-21 /pmc/articles/PMC4508635/ /pubmed/26194431 http://dx.doi.org/10.1038/srep12273 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 Fan, Hua-Ying Yang, Ming-Yan Qi, Dong Zhang, Zuo-Kai Zhu, Lin Shang-Guan, Xiu-Xin Liu, Ke Xu, Hui Che, Xin Salvianolic acid A as a multifunctional agent ameliorates doxorubicin-induced nephropathy in rats |
title | Salvianolic acid A as a multifunctional agent ameliorates doxorubicin-induced nephropathy in rats |
title_full | Salvianolic acid A as a multifunctional agent ameliorates doxorubicin-induced nephropathy in rats |
title_fullStr | Salvianolic acid A as a multifunctional agent ameliorates doxorubicin-induced nephropathy in rats |
title_full_unstemmed | Salvianolic acid A as a multifunctional agent ameliorates doxorubicin-induced nephropathy in rats |
title_short | Salvianolic acid A as a multifunctional agent ameliorates doxorubicin-induced nephropathy in rats |
title_sort | salvianolic acid a as a multifunctional agent ameliorates doxorubicin-induced nephropathy in rats |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4508635/ https://www.ncbi.nlm.nih.gov/pubmed/26194431 http://dx.doi.org/10.1038/srep12273 |
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