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Effect of Structured Phenolic Lipids with EPA/DHA and Gallic Acid against Metabolic-Associated Fatty Liver Disease (MAFLD) in Mice

Obesity is the leading risk factor for developing metabolic (dysfunction)-associated fatty liver disease (MAFLD). The food industry has an essential role in searching for new strategies to improve primary food sources to revert some of the metabolic alterations induced by obesity. There is consisten...

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Autores principales: Dovale-Rosabal, Gretel, Espinosa, Alejandra, Rodríguez, Alicia, Barriga, Andrés, Palomino-Calderón, Alan, Romero, Nalda, Troncoso, Rodrigo Hernán, Aubourg, Santiago Pedro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9696657/
https://www.ncbi.nlm.nih.gov/pubmed/36431812
http://dx.doi.org/10.3390/molecules27227702
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author Dovale-Rosabal, Gretel
Espinosa, Alejandra
Rodríguez, Alicia
Barriga, Andrés
Palomino-Calderón, Alan
Romero, Nalda
Troncoso, Rodrigo Hernán
Aubourg, Santiago Pedro
author_facet Dovale-Rosabal, Gretel
Espinosa, Alejandra
Rodríguez, Alicia
Barriga, Andrés
Palomino-Calderón, Alan
Romero, Nalda
Troncoso, Rodrigo Hernán
Aubourg, Santiago Pedro
author_sort Dovale-Rosabal, Gretel
collection PubMed
description Obesity is the leading risk factor for developing metabolic (dysfunction)-associated fatty liver disease (MAFLD). The food industry has an essential role in searching for new strategies to improve primary food sources to revert some of the metabolic alterations induced by obesity. There is consistent evidence that long-chain polyunsaturated fatty acids (n-3 LCPUFA) belonging to the n-3 series, i.e., eicosapentaenoic (20:5n-3, EPA) and docosahexaenoic (22:6n-3, DHA) acids, could revert some alterations associated with obesity-induced metabolic diseases. A relevant tool is the synthesis of structured acylglycerols (sAG), which include EPA or DHA at the sn-2 position. On the other hand, it has been reported that a crucial role of antioxidants is the reversion of MAFLD. In this work, we studied the effects of new molecules incorporating gallic acid (GA) into EPA/DHA-rich structured lipids. Mice were fed with a high-fat diet (60%) for three months and were then divided into five groups for supplementation with sAG and sAG structured with gallic acid (structured phenolic acylglycerols, sPAG). sPAG synthesis was optimized using a 2²-screening factorial design based on the response surface methodology (RSM). Our results show that treatment of sPAG was effective in decreasing visceral fat, fasting glycemia, fasting insulin, suggesting that this new molecule has a potential use in the reversal of MAFLD-associated alterations.
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spelling pubmed-96966572022-11-26 Effect of Structured Phenolic Lipids with EPA/DHA and Gallic Acid against Metabolic-Associated Fatty Liver Disease (MAFLD) in Mice Dovale-Rosabal, Gretel Espinosa, Alejandra Rodríguez, Alicia Barriga, Andrés Palomino-Calderón, Alan Romero, Nalda Troncoso, Rodrigo Hernán Aubourg, Santiago Pedro Molecules Article Obesity is the leading risk factor for developing metabolic (dysfunction)-associated fatty liver disease (MAFLD). The food industry has an essential role in searching for new strategies to improve primary food sources to revert some of the metabolic alterations induced by obesity. There is consistent evidence that long-chain polyunsaturated fatty acids (n-3 LCPUFA) belonging to the n-3 series, i.e., eicosapentaenoic (20:5n-3, EPA) and docosahexaenoic (22:6n-3, DHA) acids, could revert some alterations associated with obesity-induced metabolic diseases. A relevant tool is the synthesis of structured acylglycerols (sAG), which include EPA or DHA at the sn-2 position. On the other hand, it has been reported that a crucial role of antioxidants is the reversion of MAFLD. In this work, we studied the effects of new molecules incorporating gallic acid (GA) into EPA/DHA-rich structured lipids. Mice were fed with a high-fat diet (60%) for three months and were then divided into five groups for supplementation with sAG and sAG structured with gallic acid (structured phenolic acylglycerols, sPAG). sPAG synthesis was optimized using a 2²-screening factorial design based on the response surface methodology (RSM). Our results show that treatment of sPAG was effective in decreasing visceral fat, fasting glycemia, fasting insulin, suggesting that this new molecule has a potential use in the reversal of MAFLD-associated alterations. MDPI 2022-11-09 /pmc/articles/PMC9696657/ /pubmed/36431812 http://dx.doi.org/10.3390/molecules27227702 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Dovale-Rosabal, Gretel
Espinosa, Alejandra
Rodríguez, Alicia
Barriga, Andrés
Palomino-Calderón, Alan
Romero, Nalda
Troncoso, Rodrigo Hernán
Aubourg, Santiago Pedro
Effect of Structured Phenolic Lipids with EPA/DHA and Gallic Acid against Metabolic-Associated Fatty Liver Disease (MAFLD) in Mice
title Effect of Structured Phenolic Lipids with EPA/DHA and Gallic Acid against Metabolic-Associated Fatty Liver Disease (MAFLD) in Mice
title_full Effect of Structured Phenolic Lipids with EPA/DHA and Gallic Acid against Metabolic-Associated Fatty Liver Disease (MAFLD) in Mice
title_fullStr Effect of Structured Phenolic Lipids with EPA/DHA and Gallic Acid against Metabolic-Associated Fatty Liver Disease (MAFLD) in Mice
title_full_unstemmed Effect of Structured Phenolic Lipids with EPA/DHA and Gallic Acid against Metabolic-Associated Fatty Liver Disease (MAFLD) in Mice
title_short Effect of Structured Phenolic Lipids with EPA/DHA and Gallic Acid against Metabolic-Associated Fatty Liver Disease (MAFLD) in Mice
title_sort effect of structured phenolic lipids with epa/dha and gallic acid against metabolic-associated fatty liver disease (mafld) in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9696657/
https://www.ncbi.nlm.nih.gov/pubmed/36431812
http://dx.doi.org/10.3390/molecules27227702
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