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The influence of the intestinal microflora to the efficacy of Rosuvastatin
BACKGROUND: Intestinal microflora has been shown to play essential roles in the clinical therapies of metabolic diseases. The present study is aiming to investigate the potential roles and mechanisms of how intestinal microflora mediates lipid-reduction efficacy of Rosuvastatin. METHODS: To investig...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6026514/ https://www.ncbi.nlm.nih.gov/pubmed/29960598 http://dx.doi.org/10.1186/s12944-018-0801-x |
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author | Wang, Lijun Wang, Yang Wang, Hongwei Zhou, Xue Wei, Xianjing Xie, Zezhou Zhang, Zhipeng Wang, Keke Mu, Jianjun |
author_facet | Wang, Lijun Wang, Yang Wang, Hongwei Zhou, Xue Wei, Xianjing Xie, Zezhou Zhang, Zhipeng Wang, Keke Mu, Jianjun |
author_sort | Wang, Lijun |
collection | PubMed |
description | BACKGROUND: Intestinal microflora has been shown to play essential roles in the clinical therapies of metabolic diseases. The present study is aiming to investigate the potential roles and mechanisms of how intestinal microflora mediates lipid-reduction efficacy of Rosuvastatin. METHODS: To investigate the correlation between the intestinal microflora and efficacy of Rosuvastatin, we analyzed the diversity of intestinal microflora using PCR-DGGE analysis and 16S rDNA sequencing approaches. Furthermore, we compared the blood lipid levels of rat models with dysbiosis of intestinal microflora and control rats upon the Rosuvastatin administration. RESULTS: The diversity of the intestinal flora was obviously decreased upon the antibiotic treatment, this effect could be maintained for 2 weeks after establishment of the models. Importantly, the results from 16S rDNA sequencing demonstrated that the abundance of Lactobacillus and Bifidobacterium was remarkably diminished upon the antibiotic treatment in antibiotic+Rosuvastatin-treated group compared to that of Rosuvastatin-treated group and control group. Correspondently, the lipid-reduction efficacy of Rosuvastatin was significantly compromised. However, the diversity of the intestinal flora was recovered 4 weeks after the antibiotic treatment. Subsequently, the lipid-reduction efficacy of Rosuvastatin was also recovered to level of the control rats treated with Rosuvastatin alone. CONCLUSION: Intestinal flora could play an essential role in mediating the lipid-reduction efficacy of Rosuvastatin. |
format | Online Article Text |
id | pubmed-6026514 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-60265142018-07-09 The influence of the intestinal microflora to the efficacy of Rosuvastatin Wang, Lijun Wang, Yang Wang, Hongwei Zhou, Xue Wei, Xianjing Xie, Zezhou Zhang, Zhipeng Wang, Keke Mu, Jianjun Lipids Health Dis Research BACKGROUND: Intestinal microflora has been shown to play essential roles in the clinical therapies of metabolic diseases. The present study is aiming to investigate the potential roles and mechanisms of how intestinal microflora mediates lipid-reduction efficacy of Rosuvastatin. METHODS: To investigate the correlation between the intestinal microflora and efficacy of Rosuvastatin, we analyzed the diversity of intestinal microflora using PCR-DGGE analysis and 16S rDNA sequencing approaches. Furthermore, we compared the blood lipid levels of rat models with dysbiosis of intestinal microflora and control rats upon the Rosuvastatin administration. RESULTS: The diversity of the intestinal flora was obviously decreased upon the antibiotic treatment, this effect could be maintained for 2 weeks after establishment of the models. Importantly, the results from 16S rDNA sequencing demonstrated that the abundance of Lactobacillus and Bifidobacterium was remarkably diminished upon the antibiotic treatment in antibiotic+Rosuvastatin-treated group compared to that of Rosuvastatin-treated group and control group. Correspondently, the lipid-reduction efficacy of Rosuvastatin was significantly compromised. However, the diversity of the intestinal flora was recovered 4 weeks after the antibiotic treatment. Subsequently, the lipid-reduction efficacy of Rosuvastatin was also recovered to level of the control rats treated with Rosuvastatin alone. CONCLUSION: Intestinal flora could play an essential role in mediating the lipid-reduction efficacy of Rosuvastatin. BioMed Central 2018-06-30 /pmc/articles/PMC6026514/ /pubmed/29960598 http://dx.doi.org/10.1186/s12944-018-0801-x Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Wang, Lijun Wang, Yang Wang, Hongwei Zhou, Xue Wei, Xianjing Xie, Zezhou Zhang, Zhipeng Wang, Keke Mu, Jianjun The influence of the intestinal microflora to the efficacy of Rosuvastatin |
title | The influence of the intestinal microflora to the efficacy of Rosuvastatin |
title_full | The influence of the intestinal microflora to the efficacy of Rosuvastatin |
title_fullStr | The influence of the intestinal microflora to the efficacy of Rosuvastatin |
title_full_unstemmed | The influence of the intestinal microflora to the efficacy of Rosuvastatin |
title_short | The influence of the intestinal microflora to the efficacy of Rosuvastatin |
title_sort | influence of the intestinal microflora to the efficacy of rosuvastatin |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6026514/ https://www.ncbi.nlm.nih.gov/pubmed/29960598 http://dx.doi.org/10.1186/s12944-018-0801-x |
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