Loading…
Resveratrol transformation in red wine after heat treatment
[Display omitted] •Four resveratrol dimers were produced by oxidative coupling of resveratrol in ethanol.•Oxidative coupling reaction of resveratrol was faster and yield was higher using AgOAc.•Two of the produced dimers are reported for the first time: oxistilbenins F and G.•The compounds were iden...
Saved in:
Published in: | Food research international 2020-06, Vol.132, p.109068-109068, Article 109068 |
---|---|
Main Authors: | , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c446t-1070ee4b3e5beb46c15f7853af0f82b2cdf48b19f89f8f4c6c510165a8cb08243 |
---|---|
cites | cdi_FETCH-LOGICAL-c446t-1070ee4b3e5beb46c15f7853af0f82b2cdf48b19f89f8f4c6c510165a8cb08243 |
container_end_page | 109068 |
container_issue | |
container_start_page | 109068 |
container_title | Food research international |
container_volume | 132 |
creator | El Khawand, Toni Valls Fonayet, Josep Da Costa, Grégory Hornedo-Ortega, Ruth Jourdes, Michael Franc, Céline de Revel, Gilles Decendit, Alain Krisa, Stéphanie Richard, Tristan |
description | [Display omitted]
•Four resveratrol dimers were produced by oxidative coupling of resveratrol in ethanol.•Oxidative coupling reaction of resveratrol was faster and yield was higher using AgOAc.•Two of the produced dimers are reported for the first time: oxistilbenins F and G.•The compounds were identified and quantified in red wine after heat treatment.•The de novo synthetized compounds exhibited anti-inflammatory properties.
Resveratrol is a well-known wine constituent. Its concentration can vary according to the cultivar choice and the winemaking process. Due to its phenolic structure, resveratrol could be transformed under high temperature or oxidative conditions, leading to the formation of various derivatives including oligomers. Hence, the goal of this study is to investigate the presence of these derivatives in wine. In the first stage, hemisynthesis of oligomeric stilbenes was achieved from resveratrol in ethanol by oxidative coupling using metals. Four de novo synthetized resveratrol derivatives were identified by MS and NMR spectroscopy including two new molecules, oxistilbenin F and oxistilbenin G. In the second stage, analysis of red wine after heat treatment by LC-MS confirmed the presence of some of these compounds in wine. Finally, the anti-inflammatory effects of the compounds were evaluated by studying their ability to prevent lipopolysaccharide (LPS)-induced upregulation of nitric oxide (NO) and reactive oxygen species (ROS) production in RAW 264.7 macrophage cell line. |
doi_str_mv | 10.1016/j.foodres.2020.109068 |
format | article |
fullrecord | <record><control><sourceid>proquest_hal_p</sourceid><recordid>TN_cdi_hal_primary_oai_HAL_hal_03176116v1</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0963996920300934</els_id><sourcerecordid>2394889827</sourcerecordid><originalsourceid>FETCH-LOGICAL-c446t-1070ee4b3e5beb46c15f7853af0f82b2cdf48b19f89f8f4c6c510165a8cb08243</originalsourceid><addsrcrecordid>eNqFkMtKxDAUQIMoOj4-QelSFx2TJk0TXMgw-IIBQXQd0vQGM7SNJpkR_96Wjm6FcAOXc18HoXOC5wQTfr2eW--bAHFe4GLMSczFHpoRUdG8IqzcRzMsOc2l5PIIHce4xhjzspKH6IgWlBIuyQzdvEDcQtAp-DZLQffR-tDp5HyfuT4L0GRfrodM2wQhewedBmqIHfTpFB1Y3UY42_0n6O3-7nX5mK-eH56Wi1VuGOMpJ7jCAKymUNZQM25IaStRUm2xFUVdmMYyURNpxfAsM9yU44WlFqbGomD0BF1Nfd91qz6C63T4Vl479bhYqTGHKak4IXxLBvZyYj-C_9xATKpz0UDb6h78JqqCSiaEFEU1oOWEmuBjDGD_ehOsxg3UWu0cq9GxmhwPdRe7EZu6g-av6lfqANxOAAxStg6CisZBb6BxAUxSjXf_jPgBvjqO6Q</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2394889827</pqid></control><display><type>article</type><title>Resveratrol transformation in red wine after heat treatment</title><source>ScienceDirect Journals</source><creator>El Khawand, Toni ; Valls Fonayet, Josep ; Da Costa, Grégory ; Hornedo-Ortega, Ruth ; Jourdes, Michael ; Franc, Céline ; de Revel, Gilles ; Decendit, Alain ; Krisa, Stéphanie ; Richard, Tristan</creator><creatorcontrib>El Khawand, Toni ; Valls Fonayet, Josep ; Da Costa, Grégory ; Hornedo-Ortega, Ruth ; Jourdes, Michael ; Franc, Céline ; de Revel, Gilles ; Decendit, Alain ; Krisa, Stéphanie ; Richard, Tristan</creatorcontrib><description>[Display omitted]
•Four resveratrol dimers were produced by oxidative coupling of resveratrol in ethanol.•Oxidative coupling reaction of resveratrol was faster and yield was higher using AgOAc.•Two of the produced dimers are reported for the first time: oxistilbenins F and G.•The compounds were identified and quantified in red wine after heat treatment.•The de novo synthetized compounds exhibited anti-inflammatory properties.
Resveratrol is a well-known wine constituent. Its concentration can vary according to the cultivar choice and the winemaking process. Due to its phenolic structure, resveratrol could be transformed under high temperature or oxidative conditions, leading to the formation of various derivatives including oligomers. Hence, the goal of this study is to investigate the presence of these derivatives in wine. In the first stage, hemisynthesis of oligomeric stilbenes was achieved from resveratrol in ethanol by oxidative coupling using metals. Four de novo synthetized resveratrol derivatives were identified by MS and NMR spectroscopy including two new molecules, oxistilbenin F and oxistilbenin G. In the second stage, analysis of red wine after heat treatment by LC-MS confirmed the presence of some of these compounds in wine. Finally, the anti-inflammatory effects of the compounds were evaluated by studying their ability to prevent lipopolysaccharide (LPS)-induced upregulation of nitric oxide (NO) and reactive oxygen species (ROS) production in RAW 264.7 macrophage cell line.</description><identifier>ISSN: 0963-9969</identifier><identifier>EISSN: 1873-7145</identifier><identifier>DOI: 10.1016/j.foodres.2020.109068</identifier><identifier>PMID: 32331691</identifier><language>eng</language><publisher>Canada: Elsevier Ltd</publisher><subject>Alcoholic Beverages - analysis ; Animals ; Anti-Inflammatory Agents - pharmacology ; Anti-inflammatory effect ; Hemisynthesis ; Hot Temperature ; Life Sciences ; Lipopolysaccharides - pharmacology ; Macrophages - drug effects ; Mice ; Nitric Oxide ; Oxidative coupling ; Phenols - analysis ; RAW 264.7 Cells ; Reactive Oxygen Species ; Resveratrol ; Resveratrol - chemistry ; Resveratrol - pharmacology ; Stilbene ; Stilbenes - analysis ; Wine ; Wine - analysis</subject><ispartof>Food research international, 2020-06, Vol.132, p.109068-109068, Article 109068</ispartof><rights>2020 Elsevier Ltd</rights><rights>Copyright © 2020 Elsevier Ltd. All rights reserved.</rights><rights>Attribution - NonCommercial</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c446t-1070ee4b3e5beb46c15f7853af0f82b2cdf48b19f89f8f4c6c510165a8cb08243</citedby><cites>FETCH-LOGICAL-c446t-1070ee4b3e5beb46c15f7853af0f82b2cdf48b19f89f8f4c6c510165a8cb08243</cites><orcidid>0000-0002-5308-8697 ; 0000-0001-6509-8772</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32331691$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.inrae.fr/hal-03176116$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>El Khawand, Toni</creatorcontrib><creatorcontrib>Valls Fonayet, Josep</creatorcontrib><creatorcontrib>Da Costa, Grégory</creatorcontrib><creatorcontrib>Hornedo-Ortega, Ruth</creatorcontrib><creatorcontrib>Jourdes, Michael</creatorcontrib><creatorcontrib>Franc, Céline</creatorcontrib><creatorcontrib>de Revel, Gilles</creatorcontrib><creatorcontrib>Decendit, Alain</creatorcontrib><creatorcontrib>Krisa, Stéphanie</creatorcontrib><creatorcontrib>Richard, Tristan</creatorcontrib><title>Resveratrol transformation in red wine after heat treatment</title><title>Food research international</title><addtitle>Food Res Int</addtitle><description>[Display omitted]
•Four resveratrol dimers were produced by oxidative coupling of resveratrol in ethanol.•Oxidative coupling reaction of resveratrol was faster and yield was higher using AgOAc.•Two of the produced dimers are reported for the first time: oxistilbenins F and G.•The compounds were identified and quantified in red wine after heat treatment.•The de novo synthetized compounds exhibited anti-inflammatory properties.
Resveratrol is a well-known wine constituent. Its concentration can vary according to the cultivar choice and the winemaking process. Due to its phenolic structure, resveratrol could be transformed under high temperature or oxidative conditions, leading to the formation of various derivatives including oligomers. Hence, the goal of this study is to investigate the presence of these derivatives in wine. In the first stage, hemisynthesis of oligomeric stilbenes was achieved from resveratrol in ethanol by oxidative coupling using metals. Four de novo synthetized resveratrol derivatives were identified by MS and NMR spectroscopy including two new molecules, oxistilbenin F and oxistilbenin G. In the second stage, analysis of red wine after heat treatment by LC-MS confirmed the presence of some of these compounds in wine. Finally, the anti-inflammatory effects of the compounds were evaluated by studying their ability to prevent lipopolysaccharide (LPS)-induced upregulation of nitric oxide (NO) and reactive oxygen species (ROS) production in RAW 264.7 macrophage cell line.</description><subject>Alcoholic Beverages - analysis</subject><subject>Animals</subject><subject>Anti-Inflammatory Agents - pharmacology</subject><subject>Anti-inflammatory effect</subject><subject>Hemisynthesis</subject><subject>Hot Temperature</subject><subject>Life Sciences</subject><subject>Lipopolysaccharides - pharmacology</subject><subject>Macrophages - drug effects</subject><subject>Mice</subject><subject>Nitric Oxide</subject><subject>Oxidative coupling</subject><subject>Phenols - analysis</subject><subject>RAW 264.7 Cells</subject><subject>Reactive Oxygen Species</subject><subject>Resveratrol</subject><subject>Resveratrol - chemistry</subject><subject>Resveratrol - pharmacology</subject><subject>Stilbene</subject><subject>Stilbenes - analysis</subject><subject>Wine</subject><subject>Wine - analysis</subject><issn>0963-9969</issn><issn>1873-7145</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNqFkMtKxDAUQIMoOj4-QelSFx2TJk0TXMgw-IIBQXQd0vQGM7SNJpkR_96Wjm6FcAOXc18HoXOC5wQTfr2eW--bAHFe4GLMSczFHpoRUdG8IqzcRzMsOc2l5PIIHce4xhjzspKH6IgWlBIuyQzdvEDcQtAp-DZLQffR-tDp5HyfuT4L0GRfrodM2wQhewedBmqIHfTpFB1Y3UY42_0n6O3-7nX5mK-eH56Wi1VuGOMpJ7jCAKymUNZQM25IaStRUm2xFUVdmMYyURNpxfAsM9yU44WlFqbGomD0BF1Nfd91qz6C63T4Vl479bhYqTGHKak4IXxLBvZyYj-C_9xATKpz0UDb6h78JqqCSiaEFEU1oOWEmuBjDGD_ehOsxg3UWu0cq9GxmhwPdRe7EZu6g-av6lfqANxOAAxStg6CisZBb6BxAUxSjXf_jPgBvjqO6Q</recordid><startdate>202006</startdate><enddate>202006</enddate><creator>El Khawand, Toni</creator><creator>Valls Fonayet, Josep</creator><creator>Da Costa, Grégory</creator><creator>Hornedo-Ortega, Ruth</creator><creator>Jourdes, Michael</creator><creator>Franc, Céline</creator><creator>de Revel, Gilles</creator><creator>Decendit, Alain</creator><creator>Krisa, Stéphanie</creator><creator>Richard, Tristan</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>1XC</scope><scope>VOOES</scope><orcidid>https://orcid.org/0000-0002-5308-8697</orcidid><orcidid>https://orcid.org/0000-0001-6509-8772</orcidid></search><sort><creationdate>202006</creationdate><title>Resveratrol transformation in red wine after heat treatment</title><author>El Khawand, Toni ; Valls Fonayet, Josep ; Da Costa, Grégory ; Hornedo-Ortega, Ruth ; Jourdes, Michael ; Franc, Céline ; de Revel, Gilles ; Decendit, Alain ; Krisa, Stéphanie ; Richard, Tristan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c446t-1070ee4b3e5beb46c15f7853af0f82b2cdf48b19f89f8f4c6c510165a8cb08243</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Alcoholic Beverages - analysis</topic><topic>Animals</topic><topic>Anti-Inflammatory Agents - pharmacology</topic><topic>Anti-inflammatory effect</topic><topic>Hemisynthesis</topic><topic>Hot Temperature</topic><topic>Life Sciences</topic><topic>Lipopolysaccharides - pharmacology</topic><topic>Macrophages - drug effects</topic><topic>Mice</topic><topic>Nitric Oxide</topic><topic>Oxidative coupling</topic><topic>Phenols - analysis</topic><topic>RAW 264.7 Cells</topic><topic>Reactive Oxygen Species</topic><topic>Resveratrol</topic><topic>Resveratrol - chemistry</topic><topic>Resveratrol - pharmacology</topic><topic>Stilbene</topic><topic>Stilbenes - analysis</topic><topic>Wine</topic><topic>Wine - analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>El Khawand, Toni</creatorcontrib><creatorcontrib>Valls Fonayet, Josep</creatorcontrib><creatorcontrib>Da Costa, Grégory</creatorcontrib><creatorcontrib>Hornedo-Ortega, Ruth</creatorcontrib><creatorcontrib>Jourdes, Michael</creatorcontrib><creatorcontrib>Franc, Céline</creatorcontrib><creatorcontrib>de Revel, Gilles</creatorcontrib><creatorcontrib>Decendit, Alain</creatorcontrib><creatorcontrib>Krisa, Stéphanie</creatorcontrib><creatorcontrib>Richard, Tristan</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><jtitle>Food research international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>El Khawand, Toni</au><au>Valls Fonayet, Josep</au><au>Da Costa, Grégory</au><au>Hornedo-Ortega, Ruth</au><au>Jourdes, Michael</au><au>Franc, Céline</au><au>de Revel, Gilles</au><au>Decendit, Alain</au><au>Krisa, Stéphanie</au><au>Richard, Tristan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Resveratrol transformation in red wine after heat treatment</atitle><jtitle>Food research international</jtitle><addtitle>Food Res Int</addtitle><date>2020-06</date><risdate>2020</risdate><volume>132</volume><spage>109068</spage><epage>109068</epage><pages>109068-109068</pages><artnum>109068</artnum><issn>0963-9969</issn><eissn>1873-7145</eissn><abstract>[Display omitted]
•Four resveratrol dimers were produced by oxidative coupling of resveratrol in ethanol.•Oxidative coupling reaction of resveratrol was faster and yield was higher using AgOAc.•Two of the produced dimers are reported for the first time: oxistilbenins F and G.•The compounds were identified and quantified in red wine after heat treatment.•The de novo synthetized compounds exhibited anti-inflammatory properties.
Resveratrol is a well-known wine constituent. Its concentration can vary according to the cultivar choice and the winemaking process. Due to its phenolic structure, resveratrol could be transformed under high temperature or oxidative conditions, leading to the formation of various derivatives including oligomers. Hence, the goal of this study is to investigate the presence of these derivatives in wine. In the first stage, hemisynthesis of oligomeric stilbenes was achieved from resveratrol in ethanol by oxidative coupling using metals. Four de novo synthetized resveratrol derivatives were identified by MS and NMR spectroscopy including two new molecules, oxistilbenin F and oxistilbenin G. In the second stage, analysis of red wine after heat treatment by LC-MS confirmed the presence of some of these compounds in wine. Finally, the anti-inflammatory effects of the compounds were evaluated by studying their ability to prevent lipopolysaccharide (LPS)-induced upregulation of nitric oxide (NO) and reactive oxygen species (ROS) production in RAW 264.7 macrophage cell line.</abstract><cop>Canada</cop><pub>Elsevier Ltd</pub><pmid>32331691</pmid><doi>10.1016/j.foodres.2020.109068</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-5308-8697</orcidid><orcidid>https://orcid.org/0000-0001-6509-8772</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0963-9969 |
ispartof | Food research international, 2020-06, Vol.132, p.109068-109068, Article 109068 |
issn | 0963-9969 1873-7145 |
language | eng |
recordid | cdi_hal_primary_oai_HAL_hal_03176116v1 |
source | ScienceDirect Journals |
subjects | Alcoholic Beverages - analysis Animals Anti-Inflammatory Agents - pharmacology Anti-inflammatory effect Hemisynthesis Hot Temperature Life Sciences Lipopolysaccharides - pharmacology Macrophages - drug effects Mice Nitric Oxide Oxidative coupling Phenols - analysis RAW 264.7 Cells Reactive Oxygen Species Resveratrol Resveratrol - chemistry Resveratrol - pharmacology Stilbene Stilbenes - analysis Wine Wine - analysis |
title | Resveratrol transformation in red wine after heat treatment |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T06%3A20%3A23IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_hal_p&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Resveratrol%20transformation%20in%20red%20wine%20after%20heat%20treatment&rft.jtitle=Food%20research%20international&rft.au=El%20Khawand,%20Toni&rft.date=2020-06&rft.volume=132&rft.spage=109068&rft.epage=109068&rft.pages=109068-109068&rft.artnum=109068&rft.issn=0963-9969&rft.eissn=1873-7145&rft_id=info:doi/10.1016/j.foodres.2020.109068&rft_dat=%3Cproquest_hal_p%3E2394889827%3C/proquest_hal_p%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c446t-1070ee4b3e5beb46c15f7853af0f82b2cdf48b19f89f8f4c6c510165a8cb08243%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2394889827&rft_id=info:pmid/32331691&rfr_iscdi=true |