Cargando…
Synergistic effect of phytochemicals on cholesterol metabolism and lipid accumulation in HepG2 cells
BACKGROUND: Crocin (CRO), chlorogenic acid (CGA), geniposide (GEN), and quercetin (QUE) are all natural compounds with anti-obesity properties, in particular, hypolipidemic effects, which have been widely used for the treatment of obesity-related metabolic diseases. However, it is not yet known whet...
Autores principales: | , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5887216/ https://www.ncbi.nlm.nih.gov/pubmed/29622007 http://dx.doi.org/10.1186/s12906-018-2189-6 |
_version_ | 1783312250599112704 |
---|---|
author | Leng, Ennian Xiao, Yuan Mo, Zhentao Li, Yiqi Zhang, Yueyue Deng, Xiaosi Zhou, Min Zhou, Chaochao He, Zengxuan He, Jingyi Xiao, Lu Li, Junming Li, Wenna |
author_facet | Leng, Ennian Xiao, Yuan Mo, Zhentao Li, Yiqi Zhang, Yueyue Deng, Xiaosi Zhou, Min Zhou, Chaochao He, Zengxuan He, Jingyi Xiao, Lu Li, Junming Li, Wenna |
author_sort | Leng, Ennian |
collection | PubMed |
description | BACKGROUND: Crocin (CRO), chlorogenic acid (CGA), geniposide (GEN), and quercetin (QUE) are all natural compounds with anti-obesity properties, in particular, hypolipidemic effects, which have been widely used for the treatment of obesity-related metabolic diseases. However, it is not yet known whether these compounds interact synergistically. Here, we investigated the effects and molecular mechanisms of CRO, CGA, GEN, QUE, and a combination of all four compounds (CCGQ), on lipid accumulation in human hepatoma (HepG2 cells). METHODS: The optimal concentration of CRO, CGA, GEN, QUE to stimulate HepG2 cells proliferation was determined using MTT assay. HepG2 cells were pretreated with 10 μmol/L simvastatin, 1 μmol/L CRO, 30 μmol/L CGA, 10 μmol/L GEN, 10 μmol/L QUE, and CCGQ (a combination of 1 μmol/L CRO, 30 μmol/L CGA, 10 μmol/L GEN, and 10 μmol/L QUE) for 24 or 48 h. Oil red O staining and extracellular TC and TG levels were detected. The RT-PCR was used to observe on cholesterol metabolism-related gene expression. Immunocytochemistry and western-blot assayed the 3-hydroxy-3-methylglutaryl-coenzyme (HMGCR) protein expression in HepG2 cells. RESULTS: Compared to those of control, we demonstrated that treating HepG2 cells for 48 h with CCGQ resulted in a strong synergistic effect, causing a marked decrease in lipid deposition in comparison to individual treatments, in both triglyceride and total cholesterol (CRO, 5.74- and 1.49-folds; CGA, 3.38- and 1.12-folds; GEN, 4.04- and 1.44-folds; QUE, 3.36- and 1.24-folds; simvastatin, 5.49- and 1.83-folds; and CCGQ, 7.75- and 2.20-folds), and Oil red O staining assays. In addition, CCGQ treatment increased ATP-binding cassette transporter (ABCA1), cholesterol 7α-hydroxylase (CYP7A1), and AMP-activated protein kinase 2α (AMPKα2) mRNA expression, while decreasing sterol regulatory element binding protein 2 (SREBP2), and liver X receptor alpha (LXRα) mRNA expression. Notably, CCGQ was more effective in decreasing HMGCR expression than the individual treatments. CONCLUSION: The CCGQ combination has potential, both as a complementary therapy for hyperlipemia, and in preventing further obesity-related complications. |
format | Online Article Text |
id | pubmed-5887216 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-58872162018-04-09 Synergistic effect of phytochemicals on cholesterol metabolism and lipid accumulation in HepG2 cells Leng, Ennian Xiao, Yuan Mo, Zhentao Li, Yiqi Zhang, Yueyue Deng, Xiaosi Zhou, Min Zhou, Chaochao He, Zengxuan He, Jingyi Xiao, Lu Li, Junming Li, Wenna BMC Complement Altern Med Research Article BACKGROUND: Crocin (CRO), chlorogenic acid (CGA), geniposide (GEN), and quercetin (QUE) are all natural compounds with anti-obesity properties, in particular, hypolipidemic effects, which have been widely used for the treatment of obesity-related metabolic diseases. However, it is not yet known whether these compounds interact synergistically. Here, we investigated the effects and molecular mechanisms of CRO, CGA, GEN, QUE, and a combination of all four compounds (CCGQ), on lipid accumulation in human hepatoma (HepG2 cells). METHODS: The optimal concentration of CRO, CGA, GEN, QUE to stimulate HepG2 cells proliferation was determined using MTT assay. HepG2 cells were pretreated with 10 μmol/L simvastatin, 1 μmol/L CRO, 30 μmol/L CGA, 10 μmol/L GEN, 10 μmol/L QUE, and CCGQ (a combination of 1 μmol/L CRO, 30 μmol/L CGA, 10 μmol/L GEN, and 10 μmol/L QUE) for 24 or 48 h. Oil red O staining and extracellular TC and TG levels were detected. The RT-PCR was used to observe on cholesterol metabolism-related gene expression. Immunocytochemistry and western-blot assayed the 3-hydroxy-3-methylglutaryl-coenzyme (HMGCR) protein expression in HepG2 cells. RESULTS: Compared to those of control, we demonstrated that treating HepG2 cells for 48 h with CCGQ resulted in a strong synergistic effect, causing a marked decrease in lipid deposition in comparison to individual treatments, in both triglyceride and total cholesterol (CRO, 5.74- and 1.49-folds; CGA, 3.38- and 1.12-folds; GEN, 4.04- and 1.44-folds; QUE, 3.36- and 1.24-folds; simvastatin, 5.49- and 1.83-folds; and CCGQ, 7.75- and 2.20-folds), and Oil red O staining assays. In addition, CCGQ treatment increased ATP-binding cassette transporter (ABCA1), cholesterol 7α-hydroxylase (CYP7A1), and AMP-activated protein kinase 2α (AMPKα2) mRNA expression, while decreasing sterol regulatory element binding protein 2 (SREBP2), and liver X receptor alpha (LXRα) mRNA expression. Notably, CCGQ was more effective in decreasing HMGCR expression than the individual treatments. CONCLUSION: The CCGQ combination has potential, both as a complementary therapy for hyperlipemia, and in preventing further obesity-related complications. BioMed Central 2018-04-05 /pmc/articles/PMC5887216/ /pubmed/29622007 http://dx.doi.org/10.1186/s12906-018-2189-6 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 Article Leng, Ennian Xiao, Yuan Mo, Zhentao Li, Yiqi Zhang, Yueyue Deng, Xiaosi Zhou, Min Zhou, Chaochao He, Zengxuan He, Jingyi Xiao, Lu Li, Junming Li, Wenna Synergistic effect of phytochemicals on cholesterol metabolism and lipid accumulation in HepG2 cells |
title | Synergistic effect of phytochemicals on cholesterol metabolism and lipid accumulation in HepG2 cells |
title_full | Synergistic effect of phytochemicals on cholesterol metabolism and lipid accumulation in HepG2 cells |
title_fullStr | Synergistic effect of phytochemicals on cholesterol metabolism and lipid accumulation in HepG2 cells |
title_full_unstemmed | Synergistic effect of phytochemicals on cholesterol metabolism and lipid accumulation in HepG2 cells |
title_short | Synergistic effect of phytochemicals on cholesterol metabolism and lipid accumulation in HepG2 cells |
title_sort | synergistic effect of phytochemicals on cholesterol metabolism and lipid accumulation in hepg2 cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5887216/ https://www.ncbi.nlm.nih.gov/pubmed/29622007 http://dx.doi.org/10.1186/s12906-018-2189-6 |
work_keys_str_mv | AT lengennian synergisticeffectofphytochemicalsoncholesterolmetabolismandlipidaccumulationinhepg2cells AT xiaoyuan synergisticeffectofphytochemicalsoncholesterolmetabolismandlipidaccumulationinhepg2cells AT mozhentao synergisticeffectofphytochemicalsoncholesterolmetabolismandlipidaccumulationinhepg2cells AT liyiqi synergisticeffectofphytochemicalsoncholesterolmetabolismandlipidaccumulationinhepg2cells AT zhangyueyue synergisticeffectofphytochemicalsoncholesterolmetabolismandlipidaccumulationinhepg2cells AT dengxiaosi synergisticeffectofphytochemicalsoncholesterolmetabolismandlipidaccumulationinhepg2cells AT zhoumin synergisticeffectofphytochemicalsoncholesterolmetabolismandlipidaccumulationinhepg2cells AT zhouchaochao synergisticeffectofphytochemicalsoncholesterolmetabolismandlipidaccumulationinhepg2cells AT hezengxuan synergisticeffectofphytochemicalsoncholesterolmetabolismandlipidaccumulationinhepg2cells AT hejingyi synergisticeffectofphytochemicalsoncholesterolmetabolismandlipidaccumulationinhepg2cells AT xiaolu synergisticeffectofphytochemicalsoncholesterolmetabolismandlipidaccumulationinhepg2cells AT lijunming synergisticeffectofphytochemicalsoncholesterolmetabolismandlipidaccumulationinhepg2cells AT liwenna synergisticeffectofphytochemicalsoncholesterolmetabolismandlipidaccumulationinhepg2cells |