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Caffeine-free hawk tea lowers cholesterol by reducing free cholesterol uptake and the production of very-low-density lipoprotein

Medicinal plants show important therapeutic value in chronic disease treatment. However, due to their diverse ingredients and complex biological effects, the molecular mechanisms of medicinal plants are yet to be explored. By means of several high-throughput platforms, here we show hawk tea extract...

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Detalles Bibliográficos
Autores principales: Feng, Juan, Yang, Jian, Chang, Yujun, Qiao, Liansheng, Dang, Honglei, Luo, Kun, Guo, Hongyan, An, Yannan, Ma, Chengmei, Shao, Hong, Tian, Jie, Yuan, Yuan, Xie, Lan, Xing, Wanli, Cheng, Jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6506518/
https://www.ncbi.nlm.nih.gov/pubmed/31098406
http://dx.doi.org/10.1038/s42003-019-0396-4
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author Feng, Juan
Yang, Jian
Chang, Yujun
Qiao, Liansheng
Dang, Honglei
Luo, Kun
Guo, Hongyan
An, Yannan
Ma, Chengmei
Shao, Hong
Tian, Jie
Yuan, Yuan
Xie, Lan
Xing, Wanli
Cheng, Jing
author_facet Feng, Juan
Yang, Jian
Chang, Yujun
Qiao, Liansheng
Dang, Honglei
Luo, Kun
Guo, Hongyan
An, Yannan
Ma, Chengmei
Shao, Hong
Tian, Jie
Yuan, Yuan
Xie, Lan
Xing, Wanli
Cheng, Jing
author_sort Feng, Juan
collection PubMed
description Medicinal plants show important therapeutic value in chronic disease treatment. However, due to their diverse ingredients and complex biological effects, the molecular mechanisms of medicinal plants are yet to be explored. By means of several high-throughput platforms, here we show hawk tea extract (HTE) inhibits Niemann–Pick C1-like 1 (NPC1L1)-mediated free cholesterol uptake, thereby inducing the transcription of low-density lipoprotein receptor (LDLR) downstream of the sterol response element binding protein 2 (SREBP2) pathway. Meanwhile, HTE suppresses hepatocyte nuclear factor 4α (HNF4α)-mediated transcription of microsomal triglyceride transfer protein (MTP) and apolipoprotein B (APOB), thereby decreasing the production of very-low-density lipoprotein. The catechin EGCG ((−)-epigallocatechin gallate) and the flavonoids kaempferol and quercetin are identified as the bioactive components responsible for the effects on the NPC1L1-SREBP2-LDLR axis and HNF4α-MTP/APOB axis, respectively. Overall, hawk tea works as a previously unrecognized cholesterol-lowering agent in a multi-target and multi-component manner.
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spelling pubmed-65065182019-05-16 Caffeine-free hawk tea lowers cholesterol by reducing free cholesterol uptake and the production of very-low-density lipoprotein Feng, Juan Yang, Jian Chang, Yujun Qiao, Liansheng Dang, Honglei Luo, Kun Guo, Hongyan An, Yannan Ma, Chengmei Shao, Hong Tian, Jie Yuan, Yuan Xie, Lan Xing, Wanli Cheng, Jing Commun Biol Article Medicinal plants show important therapeutic value in chronic disease treatment. However, due to their diverse ingredients and complex biological effects, the molecular mechanisms of medicinal plants are yet to be explored. By means of several high-throughput platforms, here we show hawk tea extract (HTE) inhibits Niemann–Pick C1-like 1 (NPC1L1)-mediated free cholesterol uptake, thereby inducing the transcription of low-density lipoprotein receptor (LDLR) downstream of the sterol response element binding protein 2 (SREBP2) pathway. Meanwhile, HTE suppresses hepatocyte nuclear factor 4α (HNF4α)-mediated transcription of microsomal triglyceride transfer protein (MTP) and apolipoprotein B (APOB), thereby decreasing the production of very-low-density lipoprotein. The catechin EGCG ((−)-epigallocatechin gallate) and the flavonoids kaempferol and quercetin are identified as the bioactive components responsible for the effects on the NPC1L1-SREBP2-LDLR axis and HNF4α-MTP/APOB axis, respectively. Overall, hawk tea works as a previously unrecognized cholesterol-lowering agent in a multi-target and multi-component manner. Nature Publishing Group UK 2019-05-08 /pmc/articles/PMC6506518/ /pubmed/31098406 http://dx.doi.org/10.1038/s42003-019-0396-4 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
Feng, Juan
Yang, Jian
Chang, Yujun
Qiao, Liansheng
Dang, Honglei
Luo, Kun
Guo, Hongyan
An, Yannan
Ma, Chengmei
Shao, Hong
Tian, Jie
Yuan, Yuan
Xie, Lan
Xing, Wanli
Cheng, Jing
Caffeine-free hawk tea lowers cholesterol by reducing free cholesterol uptake and the production of very-low-density lipoprotein
title Caffeine-free hawk tea lowers cholesterol by reducing free cholesterol uptake and the production of very-low-density lipoprotein
title_full Caffeine-free hawk tea lowers cholesterol by reducing free cholesterol uptake and the production of very-low-density lipoprotein
title_fullStr Caffeine-free hawk tea lowers cholesterol by reducing free cholesterol uptake and the production of very-low-density lipoprotein
title_full_unstemmed Caffeine-free hawk tea lowers cholesterol by reducing free cholesterol uptake and the production of very-low-density lipoprotein
title_short Caffeine-free hawk tea lowers cholesterol by reducing free cholesterol uptake and the production of very-low-density lipoprotein
title_sort caffeine-free hawk tea lowers cholesterol by reducing free cholesterol uptake and the production of very-low-density lipoprotein
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6506518/
https://www.ncbi.nlm.nih.gov/pubmed/31098406
http://dx.doi.org/10.1038/s42003-019-0396-4
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