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Effect of Carotenoids from Phaeodactylum tricornutum on Palmitate-Treated HepG2 Cells
Non-alcoholic fatty liver disease represents the most common liver disease and is characterized by an excess of lipid accumulation in hepatocytes, mainly stored as triglycerides. Phaeodactylum tricornutum is a marine microalga, which is rich in bioactive molecules known to be hepatoprotective, such...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7356161/ https://www.ncbi.nlm.nih.gov/pubmed/32575640 http://dx.doi.org/10.3390/molecules25122845 |
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author | Mayer, Claire Côme, Martine Blanckaert, Vincent Chini Zittelli, Graziella Faraloni, Cecilia Nazih, Hassan Ouguerram, Khadija Mimouni, Virginie Chénais, Benoît |
author_facet | Mayer, Claire Côme, Martine Blanckaert, Vincent Chini Zittelli, Graziella Faraloni, Cecilia Nazih, Hassan Ouguerram, Khadija Mimouni, Virginie Chénais, Benoît |
author_sort | Mayer, Claire |
collection | PubMed |
description | Non-alcoholic fatty liver disease represents the most common liver disease and is characterized by an excess of lipid accumulation in hepatocytes, mainly stored as triglycerides. Phaeodactylum tricornutum is a marine microalga, which is rich in bioactive molecules known to be hepatoprotective, such as n-3 long-chain polyunsaturated fatty acids and fucoxanthin. The aim of this study was to investigate the effects of a carotenoid extract from P. tricornutum in a cellular model of non-alcoholic fatty liver disease induced by palmitate treatment. The combined effects of carotenoids and lipids, especially n-3 long-chain polyunsaturated fatty acids, were also investigated by using a total lipophilic extract. HepG2 cells were exposed for 24 h to 250 µM palmitate with or without the addition of carotenoid extract (6 μg/mL) or total lipophilic extract (100 μg/mL). The addition of carotenoid extract or total lipophilic extract prevented the accumulation of triglycerides, total cholesterol and cholesterol esters. The carotenoid extract and total lipophilic extract also decreased the mRNA expression levels of genes involved in lipogenesis (ACACA, FASN, SCD and DGAT1) and cholesterol esterification (ACAT1/SOAT1). In addition, the total lipophilic extract also downregulated the LXR/NR1H3 and SREBF1 genes, which are involved in lipogenesis regulation. By contrast, the carotenoid extract increased the mRNA level of CPT1A, a β-oxidation related gene, and reduced the lipid droplet accumulation. In conclusion, this study highlights the preventive effects against non-alcoholic fatty liver disease of the two microalga extracts. |
format | Online Article Text |
id | pubmed-7356161 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-73561612020-07-31 Effect of Carotenoids from Phaeodactylum tricornutum on Palmitate-Treated HepG2 Cells Mayer, Claire Côme, Martine Blanckaert, Vincent Chini Zittelli, Graziella Faraloni, Cecilia Nazih, Hassan Ouguerram, Khadija Mimouni, Virginie Chénais, Benoît Molecules Article Non-alcoholic fatty liver disease represents the most common liver disease and is characterized by an excess of lipid accumulation in hepatocytes, mainly stored as triglycerides. Phaeodactylum tricornutum is a marine microalga, which is rich in bioactive molecules known to be hepatoprotective, such as n-3 long-chain polyunsaturated fatty acids and fucoxanthin. The aim of this study was to investigate the effects of a carotenoid extract from P. tricornutum in a cellular model of non-alcoholic fatty liver disease induced by palmitate treatment. The combined effects of carotenoids and lipids, especially n-3 long-chain polyunsaturated fatty acids, were also investigated by using a total lipophilic extract. HepG2 cells were exposed for 24 h to 250 µM palmitate with or without the addition of carotenoid extract (6 μg/mL) or total lipophilic extract (100 μg/mL). The addition of carotenoid extract or total lipophilic extract prevented the accumulation of triglycerides, total cholesterol and cholesterol esters. The carotenoid extract and total lipophilic extract also decreased the mRNA expression levels of genes involved in lipogenesis (ACACA, FASN, SCD and DGAT1) and cholesterol esterification (ACAT1/SOAT1). In addition, the total lipophilic extract also downregulated the LXR/NR1H3 and SREBF1 genes, which are involved in lipogenesis regulation. By contrast, the carotenoid extract increased the mRNA level of CPT1A, a β-oxidation related gene, and reduced the lipid droplet accumulation. In conclusion, this study highlights the preventive effects against non-alcoholic fatty liver disease of the two microalga extracts. MDPI 2020-06-19 /pmc/articles/PMC7356161/ /pubmed/32575640 http://dx.doi.org/10.3390/molecules25122845 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Mayer, Claire Côme, Martine Blanckaert, Vincent Chini Zittelli, Graziella Faraloni, Cecilia Nazih, Hassan Ouguerram, Khadija Mimouni, Virginie Chénais, Benoît Effect of Carotenoids from Phaeodactylum tricornutum on Palmitate-Treated HepG2 Cells |
title | Effect of Carotenoids from Phaeodactylum tricornutum on Palmitate-Treated HepG2 Cells |
title_full | Effect of Carotenoids from Phaeodactylum tricornutum on Palmitate-Treated HepG2 Cells |
title_fullStr | Effect of Carotenoids from Phaeodactylum tricornutum on Palmitate-Treated HepG2 Cells |
title_full_unstemmed | Effect of Carotenoids from Phaeodactylum tricornutum on Palmitate-Treated HepG2 Cells |
title_short | Effect of Carotenoids from Phaeodactylum tricornutum on Palmitate-Treated HepG2 Cells |
title_sort | effect of carotenoids from phaeodactylum tricornutum on palmitate-treated hepg2 cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7356161/ https://www.ncbi.nlm.nih.gov/pubmed/32575640 http://dx.doi.org/10.3390/molecules25122845 |
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