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Liver-target nanotechnology facilitates berberine to ameliorate cardio-metabolic diseases
Cardiovascular and metabolic disease (CMD) remains a main cause of premature death worldwide. Berberine (BBR), a lipid-lowering botanic compound with diversified potency against metabolic disorders, is a promising candidate for ameliorating CMD. The liver is the target of BBR so that liver-site accu...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6491597/ https://www.ncbi.nlm.nih.gov/pubmed/31040273 http://dx.doi.org/10.1038/s41467-019-09852-0 |
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author | Guo, Hui-Hui Feng, Chen-Lin Zhang, Wen-Xuan Luo, Zhi-Gang Zhang, Hong-Juan Zhang, Ting-Ting Ma, Chen Zhan, Yun Li, Rui Wu, Song Abliz, Zeper Li, Cong Li, Xiao-Lin Ma, Xiao-Lei Wang, Lu-Lu Zheng, Wen-Sheng Han, Yan-Xing Jiang, Jian-Dong |
author_facet | Guo, Hui-Hui Feng, Chen-Lin Zhang, Wen-Xuan Luo, Zhi-Gang Zhang, Hong-Juan Zhang, Ting-Ting Ma, Chen Zhan, Yun Li, Rui Wu, Song Abliz, Zeper Li, Cong Li, Xiao-Lin Ma, Xiao-Lei Wang, Lu-Lu Zheng, Wen-Sheng Han, Yan-Xing Jiang, Jian-Dong |
author_sort | Guo, Hui-Hui |
collection | PubMed |
description | Cardiovascular and metabolic disease (CMD) remains a main cause of premature death worldwide. Berberine (BBR), a lipid-lowering botanic compound with diversified potency against metabolic disorders, is a promising candidate for ameliorating CMD. The liver is the target of BBR so that liver-site accumulation could be important for fulfilling its therapeutic effect. In this study a rational designed micelle (CTA-Mic) consisting of α-tocopheryl hydrophobic core and on-site detachable polyethylene glycol-thiol shell is developed for effective liver deposition of BBR. The bio-distribution analysis proves that the accumulation of BBR in liver is increased by 248.8% assisted by micelles. Up-regulation of a range of energy-related genes is detectable in the HepG2 cells and in vivo. In the high fat diet-fed mice, BBR-CTA-Mic intervention remarkably improves metabolic profiles and reduces the formation of aortic arch plaque. Our results provide proof-of-concept for a liver-targeting strategy to ameliorate CMD using natural medicines facilitated by Nano-technology. |
format | Online Article Text |
id | pubmed-6491597 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64915972019-05-02 Liver-target nanotechnology facilitates berberine to ameliorate cardio-metabolic diseases Guo, Hui-Hui Feng, Chen-Lin Zhang, Wen-Xuan Luo, Zhi-Gang Zhang, Hong-Juan Zhang, Ting-Ting Ma, Chen Zhan, Yun Li, Rui Wu, Song Abliz, Zeper Li, Cong Li, Xiao-Lin Ma, Xiao-Lei Wang, Lu-Lu Zheng, Wen-Sheng Han, Yan-Xing Jiang, Jian-Dong Nat Commun Article Cardiovascular and metabolic disease (CMD) remains a main cause of premature death worldwide. Berberine (BBR), a lipid-lowering botanic compound with diversified potency against metabolic disorders, is a promising candidate for ameliorating CMD. The liver is the target of BBR so that liver-site accumulation could be important for fulfilling its therapeutic effect. In this study a rational designed micelle (CTA-Mic) consisting of α-tocopheryl hydrophobic core and on-site detachable polyethylene glycol-thiol shell is developed for effective liver deposition of BBR. The bio-distribution analysis proves that the accumulation of BBR in liver is increased by 248.8% assisted by micelles. Up-regulation of a range of energy-related genes is detectable in the HepG2 cells and in vivo. In the high fat diet-fed mice, BBR-CTA-Mic intervention remarkably improves metabolic profiles and reduces the formation of aortic arch plaque. Our results provide proof-of-concept for a liver-targeting strategy to ameliorate CMD using natural medicines facilitated by Nano-technology. Nature Publishing Group UK 2019-04-30 /pmc/articles/PMC6491597/ /pubmed/31040273 http://dx.doi.org/10.1038/s41467-019-09852-0 Text en © The Author(s) 2019 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Guo, Hui-Hui Feng, Chen-Lin Zhang, Wen-Xuan Luo, Zhi-Gang Zhang, Hong-Juan Zhang, Ting-Ting Ma, Chen Zhan, Yun Li, Rui Wu, Song Abliz, Zeper Li, Cong Li, Xiao-Lin Ma, Xiao-Lei Wang, Lu-Lu Zheng, Wen-Sheng Han, Yan-Xing Jiang, Jian-Dong Liver-target nanotechnology facilitates berberine to ameliorate cardio-metabolic diseases |
title | Liver-target nanotechnology facilitates berberine to ameliorate cardio-metabolic diseases |
title_full | Liver-target nanotechnology facilitates berberine to ameliorate cardio-metabolic diseases |
title_fullStr | Liver-target nanotechnology facilitates berberine to ameliorate cardio-metabolic diseases |
title_full_unstemmed | Liver-target nanotechnology facilitates berberine to ameliorate cardio-metabolic diseases |
title_short | Liver-target nanotechnology facilitates berberine to ameliorate cardio-metabolic diseases |
title_sort | liver-target nanotechnology facilitates berberine to ameliorate cardio-metabolic diseases |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6491597/ https://www.ncbi.nlm.nih.gov/pubmed/31040273 http://dx.doi.org/10.1038/s41467-019-09852-0 |
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