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Gut Microbiota-Mediated Personalized Treatment of Hyperlipidemia Using Berberine
Nitroreductases (NRs) are bacterial enzymes that reduce nitro-containing compounds. We have previously reported that NR of intestinal bacteria is a key factor promoting berberine (BBR) intestinal absorption. We show here that feeding hamsters with high fat diet (HFD) caused an increase in blood lipi...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5525748/ https://www.ncbi.nlm.nih.gov/pubmed/28744326 http://dx.doi.org/10.7150/thno.18290 |
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author | Wang, Yan Tong, Qian Shou, Jia-Wen Zhao, Zhen-Xiong Li, Xiao-Yang Zhang, Xian-Feng Ma, Shu-Rong He, Chi-Yu Lin, Yuan Wen, Bao-Ying Guo, Fang Fu, Jie Jiang, Jian-Dong |
author_facet | Wang, Yan Tong, Qian Shou, Jia-Wen Zhao, Zhen-Xiong Li, Xiao-Yang Zhang, Xian-Feng Ma, Shu-Rong He, Chi-Yu Lin, Yuan Wen, Bao-Ying Guo, Fang Fu, Jie Jiang, Jian-Dong |
author_sort | Wang, Yan |
collection | PubMed |
description | Nitroreductases (NRs) are bacterial enzymes that reduce nitro-containing compounds. We have previously reported that NR of intestinal bacteria is a key factor promoting berberine (BBR) intestinal absorption. We show here that feeding hamsters with high fat diet (HFD) caused an increase in blood lipids and NR activity in the intestine. The elevation of fecal NR by HFD was due to the increase in either the fraction of NR-producing bacteria or their activity in the intestine. When given orally, BBR bioavailability in the HFD-fed hamsters was higher than that in those fed with normal chow (by +72%, *P<0.05). BBR (100 mg/kg/day, orally) decreased blood lipids in the HFD-fed hamsters (**P<0.01) but not in those fed with normal diet. Clinical studies indicated that patients with hyperlipidemia had higher fecal NR activity than that in the healthy individuals (**P<0.01). Similarly, after oral administration, the blood level of BBR in hyperlipidemic patients was higher than that in healthy individuals (*P<0.05). Correlation analysis revealed a positive relationship between blood BBR and fecal NR activity (r=0.703). Thus, the fecal NR activity might serve as a biomarker in the personalized treatment of hyperlipidemia using BBR. |
format | Online Article Text |
id | pubmed-5525748 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-55257482017-07-25 Gut Microbiota-Mediated Personalized Treatment of Hyperlipidemia Using Berberine Wang, Yan Tong, Qian Shou, Jia-Wen Zhao, Zhen-Xiong Li, Xiao-Yang Zhang, Xian-Feng Ma, Shu-Rong He, Chi-Yu Lin, Yuan Wen, Bao-Ying Guo, Fang Fu, Jie Jiang, Jian-Dong Theranostics Research Paper Nitroreductases (NRs) are bacterial enzymes that reduce nitro-containing compounds. We have previously reported that NR of intestinal bacteria is a key factor promoting berberine (BBR) intestinal absorption. We show here that feeding hamsters with high fat diet (HFD) caused an increase in blood lipids and NR activity in the intestine. The elevation of fecal NR by HFD was due to the increase in either the fraction of NR-producing bacteria or their activity in the intestine. When given orally, BBR bioavailability in the HFD-fed hamsters was higher than that in those fed with normal chow (by +72%, *P<0.05). BBR (100 mg/kg/day, orally) decreased blood lipids in the HFD-fed hamsters (**P<0.01) but not in those fed with normal diet. Clinical studies indicated that patients with hyperlipidemia had higher fecal NR activity than that in the healthy individuals (**P<0.01). Similarly, after oral administration, the blood level of BBR in hyperlipidemic patients was higher than that in healthy individuals (*P<0.05). Correlation analysis revealed a positive relationship between blood BBR and fecal NR activity (r=0.703). Thus, the fecal NR activity might serve as a biomarker in the personalized treatment of hyperlipidemia using BBR. Ivyspring International Publisher 2017-06-24 /pmc/articles/PMC5525748/ /pubmed/28744326 http://dx.doi.org/10.7150/thno.18290 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Research Paper Wang, Yan Tong, Qian Shou, Jia-Wen Zhao, Zhen-Xiong Li, Xiao-Yang Zhang, Xian-Feng Ma, Shu-Rong He, Chi-Yu Lin, Yuan Wen, Bao-Ying Guo, Fang Fu, Jie Jiang, Jian-Dong Gut Microbiota-Mediated Personalized Treatment of Hyperlipidemia Using Berberine |
title | Gut Microbiota-Mediated Personalized Treatment of Hyperlipidemia Using Berberine |
title_full | Gut Microbiota-Mediated Personalized Treatment of Hyperlipidemia Using Berberine |
title_fullStr | Gut Microbiota-Mediated Personalized Treatment of Hyperlipidemia Using Berberine |
title_full_unstemmed | Gut Microbiota-Mediated Personalized Treatment of Hyperlipidemia Using Berberine |
title_short | Gut Microbiota-Mediated Personalized Treatment of Hyperlipidemia Using Berberine |
title_sort | gut microbiota-mediated personalized treatment of hyperlipidemia using berberine |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5525748/ https://www.ncbi.nlm.nih.gov/pubmed/28744326 http://dx.doi.org/10.7150/thno.18290 |
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