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Red yeast rice repairs kidney damage and reduces inflammatory transcription factors in rat models of hyperlipidemia
Xuezhikang (XZK), an extract of red yeast rice, has been widely used for the management of hyperlipidemia and coronary heart disease (CHD); however, the effects of XZK treatment on kidney injury have not yet been fully identified. The aim of the current study was to evaluate the effects of XZK on th...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4217782/ https://www.ncbi.nlm.nih.gov/pubmed/25371725 http://dx.doi.org/10.3892/etm.2014.2035 |
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author | DING, MEI SI, DAOYUAN ZHANG, WENQI FENG, ZHAOHUI HE, MIN YANG, PING |
author_facet | DING, MEI SI, DAOYUAN ZHANG, WENQI FENG, ZHAOHUI HE, MIN YANG, PING |
author_sort | DING, MEI |
collection | PubMed |
description | Xuezhikang (XZK), an extract of red yeast rice, has been widely used for the management of hyperlipidemia and coronary heart disease (CHD); however, the effects of XZK treatment on kidney injury have not yet been fully identified. The aim of the current study was to evaluate the effects of XZK on the kidneys and investigate the related mechanisms in a rat model of hyperlipidemia. Thus, the effect on inflammatory transcription factors and kidney damage was investigated with in vitro and in vivo experiments on hyperlipidemic rats following XZK treatment. The results revealed that the plasma levels of total cholesterol (TC), triglycerides (TG) and low-density lipoprotein-cholesterol (LDL-C) were significantly decreased, while the levels of high-density lipoprotein-cholesterol (HDL-C) were significantly upregulated in the XZK treatment group, as compared with those in the hyperlipidemia group (P<0.05). In addition, the results demonstrated that XZK was able to repair the kidney damage caused by hyperlipidemia. Furthermore, the expression levels of the inflammatory transcription factors, tumor necrosis factor-α and interleukin-6, were shown to be reduced in the XZK group when compared with the hyperlipidemia group. In summary, XZK reduces kidney injury, downregulates the levels of TG, TC and LDL-C, as well as the expression levels of inflammatory transcription factors, and upregulates HDL-C. These results further the understanding of the molecular pathogenic mechanisms underlying hyperlipidemia and aid the development of XZK as an effective therapeutic agent for hyperlipidemia. |
format | Online Article Text |
id | pubmed-4217782 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-42177822014-11-04 Red yeast rice repairs kidney damage and reduces inflammatory transcription factors in rat models of hyperlipidemia DING, MEI SI, DAOYUAN ZHANG, WENQI FENG, ZHAOHUI HE, MIN YANG, PING Exp Ther Med Articles Xuezhikang (XZK), an extract of red yeast rice, has been widely used for the management of hyperlipidemia and coronary heart disease (CHD); however, the effects of XZK treatment on kidney injury have not yet been fully identified. The aim of the current study was to evaluate the effects of XZK on the kidneys and investigate the related mechanisms in a rat model of hyperlipidemia. Thus, the effect on inflammatory transcription factors and kidney damage was investigated with in vitro and in vivo experiments on hyperlipidemic rats following XZK treatment. The results revealed that the plasma levels of total cholesterol (TC), triglycerides (TG) and low-density lipoprotein-cholesterol (LDL-C) were significantly decreased, while the levels of high-density lipoprotein-cholesterol (HDL-C) were significantly upregulated in the XZK treatment group, as compared with those in the hyperlipidemia group (P<0.05). In addition, the results demonstrated that XZK was able to repair the kidney damage caused by hyperlipidemia. Furthermore, the expression levels of the inflammatory transcription factors, tumor necrosis factor-α and interleukin-6, were shown to be reduced in the XZK group when compared with the hyperlipidemia group. In summary, XZK reduces kidney injury, downregulates the levels of TG, TC and LDL-C, as well as the expression levels of inflammatory transcription factors, and upregulates HDL-C. These results further the understanding of the molecular pathogenic mechanisms underlying hyperlipidemia and aid the development of XZK as an effective therapeutic agent for hyperlipidemia. D.A. Spandidos 2014-12 2014-10-21 /pmc/articles/PMC4217782/ /pubmed/25371725 http://dx.doi.org/10.3892/etm.2014.2035 Text en Copyright © 2014, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited. |
spellingShingle | Articles DING, MEI SI, DAOYUAN ZHANG, WENQI FENG, ZHAOHUI HE, MIN YANG, PING Red yeast rice repairs kidney damage and reduces inflammatory transcription factors in rat models of hyperlipidemia |
title | Red yeast rice repairs kidney damage and reduces inflammatory transcription factors in rat models of hyperlipidemia |
title_full | Red yeast rice repairs kidney damage and reduces inflammatory transcription factors in rat models of hyperlipidemia |
title_fullStr | Red yeast rice repairs kidney damage and reduces inflammatory transcription factors in rat models of hyperlipidemia |
title_full_unstemmed | Red yeast rice repairs kidney damage and reduces inflammatory transcription factors in rat models of hyperlipidemia |
title_short | Red yeast rice repairs kidney damage and reduces inflammatory transcription factors in rat models of hyperlipidemia |
title_sort | red yeast rice repairs kidney damage and reduces inflammatory transcription factors in rat models of hyperlipidemia |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4217782/ https://www.ncbi.nlm.nih.gov/pubmed/25371725 http://dx.doi.org/10.3892/etm.2014.2035 |
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