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High protection by grape seed proanthocyanidins (GSPC) of polyunsaturated fatty acids against UV-C induced peroxidation

Identifieur interne : 000555 ( Istex/Corpus ); précédent : 000554; suivant : 000556

High protection by grape seed proanthocyanidins (GSPC) of polyunsaturated fatty acids against UV-C induced peroxidation

Auteurs : Rachid Bouhamidi ; Virginie Prévost ; André Nouvelot

Source :

RBID : ISTEX:3792FB74D0E7B6FA8A00C137A0997A0C6F9618BC

English descriptors

Abstract

Abstract: The antioxidative effects of grape seed proanthocyanidins (GSPC) were studied in three in-vitro models in which polyunsaturated fatty acids (PUFAs) in aqueous solution and mice liver or brain microsomes were used as oxidative substrates, and UVC irradiation as the pro-oxidant system. Analysis of UV-C induced lipid peroxidation was carried out by two methods: gas liquid chromatography of residual PUFAs and release of thiobarbituric acid-reactive substances (TBARs) measured by TBA reaction. Results indicate that PUFAs are more radiosensitive when incorporated in single component micelles than in mixed component micelles or microsomes. In every case, PUFA peroxidation was inhibited by low concentrations of GSPC (2 rng/L) while epigallocatecin (EGC) and epigallocatechin gallate (EGCG) monomers, at an equivalent level of epicatechin, exhibited no efficacy in our experimental conditions. This latter effect might be explained by a synergistic action of flavan-3-ol monomers, dimers and oligomers contained in the grape seed extract.

Url:
DOI: 10.1016/S0764-4469(97)89623-0

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ISTEX:3792FB74D0E7B6FA8A00C137A0997A0C6F9618BC

Le document en format XML

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<ce:alt-title xml:lang="fr">Haute protection par les proanthocyanidines de pépins de raisin contre la peroxydation des acides gras polyinsaturés induite par les UV-C</ce:alt-title>
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<ce:given-name>Rachid</ce:given-name>
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<ce:surname>Prévost</ce:surname>
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<ce:simple-para>The antioxidative effects of grape seed proanthocyanidins (GSPC) were studied in three in-vitro models in which polyunsaturated fatty acids (PUFAs) in aqueous solution and mice liver or brain microsomes were used as oxidative substrates, and UVC irradiation as the pro-oxidant system. Analysis of UV-C induced lipid peroxidation was carried out by two methods: gas liquid chromatography of residual PUFAs and release of thiobarbituric acid-reactive substances (TBARs) measured by TBA reaction. Results indicate that PUFAs are more radiosensitive when incorporated in single component micelles than in mixed component micelles or microsomes. In every case, PUFA peroxidation was inhibited by low concentrations of GSPC (2 rng/L) while epigallocatecin (EGC) and epigallocatechin gallate (EGCG) monomers, at an equivalent level of epicatechin, exhibited no efficacy in our experimental conditions. This latter effect might be explained by a synergistic action of flavan-3-ol monomers, dimers and oligomers contained in the grape seed extract.</ce:simple-para>
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<ce:simple-para>Résumé Resume L'effet antioxydant des proanthocyanidines de pépins de raisin a été étudié dans trois modèles in vitro. Des acides gras polyinsaturés (AGPI) en solution aqueuse ou des microsomes de foie et de cerveau de souris ont été utilisés comme substrats et l'irradiation UV-C comme système prooxydant. La peroxydation lipidique induite par les UV-C a été mesurée par deux méthodes: le dosage des AGPI résiduels par chromatographie en phase gazeuse et le dosage des substances réagissant avec lacide thiobarbiturique par la technique de 1 BA-réaction. Les résultats indiquent que les AGPI sont plus radiosensibles lorsqu'ils sont incorporés dans des micelles simples que lorsqu'ils sont incorporés dans des micelles contenant plusieurs AGPI ou des microsomes. Dans tous les cas, la peroxydation des AGPI est inhibée par de faibles concentrations de l'extrait proanthocyanidolique (2 mg/L) alors que l'épigallocatéchine et l'épigallocatéchine-gallate sous forme de monomères ne montrent aucune efficacité dans ces conditions expérimentales. Cela pourrait être expliqué par une action synergique des flavanes-3-ol monomères, dimères et trimères constituant l'extrait proanthocyanidolique de pépins de raisin.</ce:simple-para>
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<ce:surname>Fontecave</ce:surname>
<ce:given-name>M.</ce:given-name>
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<dateIssued encoding="w3cdtf">1998</dateIssued>
<copyrightDate encoding="w3cdtf">1998</copyrightDate>
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<languageTerm type="code" authority="iso639-2b">eng</languageTerm>
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<abstract lang="en">Abstract: The antioxidative effects of grape seed proanthocyanidins (GSPC) were studied in three in-vitro models in which polyunsaturated fatty acids (PUFAs) in aqueous solution and mice liver or brain microsomes were used as oxidative substrates, and UVC irradiation as the pro-oxidant system. Analysis of UV-C induced lipid peroxidation was carried out by two methods: gas liquid chromatography of residual PUFAs and release of thiobarbituric acid-reactive substances (TBARs) measured by TBA reaction. Results indicate that PUFAs are more radiosensitive when incorporated in single component micelles than in mixed component micelles or microsomes. In every case, PUFA peroxidation was inhibited by low concentrations of GSPC (2 rng/L) while epigallocatecin (EGC) and epigallocatechin gallate (EGCG) monomers, at an equivalent level of epicatechin, exhibited no efficacy in our experimental conditions. This latter effect might be explained by a synergistic action of flavan-3-ol monomers, dimers and oligomers contained in the grape seed extract.</abstract>
<abstract lang="fr">Résumé Resume L'effet antioxydant des proanthocyanidines de pépins de raisin a été étudié dans trois modèles in vitro. Des acides gras polyinsaturés (AGPI) en solution aqueuse ou des microsomes de foie et de cerveau de souris ont été utilisés comme substrats et l'irradiation UV-C comme système prooxydant. La peroxydation lipidique induite par les UV-C a été mesurée par deux méthodes: le dosage des AGPI résiduels par chromatographie en phase gazeuse et le dosage des substances réagissant avec lacide thiobarbiturique par la technique de 1 BA-réaction. Les résultats indiquent que les AGPI sont plus radiosensibles lorsqu'ils sont incorporés dans des micelles simples que lorsqu'ils sont incorporés dans des micelles contenant plusieurs AGPI ou des microsomes. Dans tous les cas, la peroxydation des AGPI est inhibée par de faibles concentrations de l'extrait proanthocyanidolique (2 mg/L) alors que l'épigallocatéchine et l'épigallocatéchine-gallate sous forme de monomères ne montrent aucune efficacité dans ces conditions expérimentales. Cela pourrait être expliqué par une action synergique des flavanes-3-ol monomères, dimères et trimères constituant l'extrait proanthocyanidolique de pépins de raisin.</abstract>
<note>*</note>
<note type="content">Section title: Plant biology and pathology</note>
<subject lang="en">
<topic>polyunsaturated fatty acids</topic>
<topic>UV-C rays</topic>
<topic>lipoperoxidation</topic>
<topic>proanthocyanidins</topic>
<topic>grape seeds</topic>
</subject>
<subject lang="fr">
<topic>acides gras polyinsaturés</topic>
<topic>rayons UV-C</topic>
<topic>lipoperoxydation</topic>
<topic>proanthocyanidines</topic>
<topic>pépins de raisin</topic>
</subject>
<relatedItem type="host">
<titleInfo>
<title>Comptes Rendus de l'Academie des Sciences Series III Sciences de la Vie</title>
</titleInfo>
<titleInfo type="abbreviated">
<title>PXVOLD</title>
</titleInfo>
<genre type="journal">journal</genre>
<originInfo>
<dateIssued encoding="w3cdtf">199801</dateIssued>
</originInfo>
<identifier type="ISSN">0764-4469</identifier>
<identifier type="PII">S0764-4469(00)X0035-2</identifier>
<part>
<date>199801</date>
<detail type="volume">
<number>321</number>
<caption>vol.</caption>
</detail>
<detail type="issue">
<number>1</number>
<caption>no.</caption>
</detail>
<extent unit="issue pages">
<start>1</start>
<end>85</end>
</extent>
<extent unit="pages">
<start>31</start>
<end>38</end>
</extent>
</part>
</relatedItem>
<identifier type="istex">3792FB74D0E7B6FA8A00C137A0997A0C6F9618BC</identifier>
<identifier type="DOI">10.1016/S0764-4469(97)89623-0</identifier>
<identifier type="PII">S0764-4469(97)89623-0</identifier>
<identifier type="ArticleID">97896230</identifier>
<accessCondition type="use and reproduction" contentType="copyright">©1998 Académie des sciences / Elsevier</accessCondition>
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<recordOrigin>Académie des sciences / Elsevier, ©1998</recordOrigin>
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