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In Vitro Dermo-Cosmetic Evaluation of Bark Extracts from Common Temperate Trees.

Identifieur interne : 001813 ( Main/Exploration ); précédent : 001812; suivant : 001814

In Vitro Dermo-Cosmetic Evaluation of Bark Extracts from Common Temperate Trees.

Auteurs : Jane Hubert [France] ; Apostolis Angelis [France] ; Nektarios Aligiannis [Grèce] ; Michalea Rosalia [Grèce] ; Amin Abedini [France] ; Ali Bakiri [France] ; Romain Reynaud [France] ; Jean-Marc Nuzillard [France] ; Sophie C. Gangloff [France] ; Alexios-Leandros Skaltsounis [Grèce] ; Jean-Hugues Renault [France]

Source :

RBID : pubmed:27352384

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English descriptors

Abstract

Wood residues produced from forestry activities represent an interesting source of biologically active, high value-added secondary metabolites. In this study, 30 extracts from 10 barks of deciduous and coniferous tree species were investigated for their potential dermo-cosmetic use. The extracts were obtained from Fagus sylvatica, Quercus robur, Alnus glutinosa, Prunus avium, Acer pseudoplatanus, Fraxinus excelsior, Populus robusta, Larix decidua, Picea abies, and Populus tremula after three successive solid/liquid extractions of the barks with n-heptane, methanol, and methanol/water. All extracts were evaluated for their radical scavenging capacity, for their elastase, collagenase, and tyrosinase inhibitory activities, as well as for their antibacterial activity against gram-positive Staphylococcus aureus. In parallel, the global metabolite profiles of all extracts were established by 1D and 2D NMR and related to their biological activity. The results showed that the methanol extracts of Q. robur, A. glutinosa, L. decidua, and P. abies barks exhibit particularly high activities on most bioassays, suggesting their promising use as active ingredients in the dermo-cosmetic industry.

DOI: 10.1055/s-0042-110180
PubMed: 27352384


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Le document en format XML

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<term>Animals (MeSH)</term>
<term>Anti-Bacterial Agents (pharmacology)</term>
<term>Dermatologic Agents (chemistry)</term>
<term>Dermatologic Agents (pharmacology)</term>
<term>Drug Evaluation, Preclinical (methods)</term>
<term>Enzyme Inhibitors (chemistry)</term>
<term>Enzyme Inhibitors (pharmacology)</term>
<term>Magnetic Resonance Spectroscopy (MeSH)</term>
<term>Monophenol Monooxygenase (antagonists & inhibitors)</term>
<term>Pancreatic Elastase (antagonists & inhibitors)</term>
<term>Plant Bark (chemistry)</term>
<term>Plant Extracts (chemistry)</term>
<term>Plant Extracts (pharmacology)</term>
<term>Staphylococcus aureus (drug effects)</term>
<term>Trees (chemistry)</term>
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<term>Animaux (MeSH)</term>
<term>Antibactériens (pharmacologie)</term>
<term>Antienzymes (composition chimique)</term>
<term>Antienzymes (pharmacologie)</term>
<term>Arbres (composition chimique)</term>
<term>Extraits de plantes (composition chimique)</term>
<term>Extraits de plantes (pharmacologie)</term>
<term>Monophenol monooxygenase (antagonistes et inhibiteurs)</term>
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<term>Produits dermatologiques (composition chimique)</term>
<term>Produits dermatologiques (pharmacologie)</term>
<term>Spectroscopie par résonance magnétique (MeSH)</term>
<term>Staphylococcus aureus (effets des médicaments et des substances chimiques)</term>
<term>Écorce (composition chimique)</term>
<term>Évaluation préclinique de médicament (méthodes)</term>
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</keywords>
<keywords scheme="MESH" qualifier="composition chimique" xml:lang="fr">
<term>Antienzymes</term>
<term>Arbres</term>
<term>Extraits de plantes</term>
<term>Produits dermatologiques</term>
<term>Écorce</term>
</keywords>
<keywords scheme="MESH" qualifier="drug effects" xml:lang="en">
<term>Staphylococcus aureus</term>
</keywords>
<keywords scheme="MESH" qualifier="effets des médicaments et des substances chimiques" xml:lang="fr">
<term>Staphylococcus aureus</term>
</keywords>
<keywords scheme="MESH" qualifier="methods" xml:lang="en">
<term>Drug Evaluation, Preclinical</term>
</keywords>
<keywords scheme="MESH" qualifier="méthodes" xml:lang="fr">
<term>Évaluation préclinique de médicament</term>
</keywords>
<keywords scheme="MESH" qualifier="pharmacologie" xml:lang="fr">
<term>Antibactériens</term>
<term>Antienzymes</term>
<term>Extraits de plantes</term>
<term>Produits dermatologiques</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Animals</term>
<term>Magnetic Resonance Spectroscopy</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Animaux</term>
<term>Spectroscopie par résonance magnétique</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">Wood residues produced from forestry activities represent an interesting source of biologically active, high value-added secondary metabolites. In this study, 30 extracts from 10 barks of deciduous and coniferous tree species were investigated for their potential dermo-cosmetic use. The extracts were obtained from
<i>Fagus sylvatica, Quercus robur, Alnus glutinosa, Prunus avium, Acer pseudoplatanus, Fraxinus excelsior, Populus robusta, Larix decidua, Picea abies</i>
, and
<i>Populus tremula</i>
after three successive solid/liquid extractions of the barks with
<i>n-</i>
heptane, methanol, and methanol/water. All extracts were evaluated for their radical scavenging capacity, for their elastase, collagenase, and tyrosinase inhibitory activities, as well as for their antibacterial activity against gram-positive
<i>Staphylococcus aureus</i>
. In parallel, the global metabolite profiles of all extracts were established by 1D and 2D NMR and related to their biological activity. The results showed that the methanol extracts of
<i>Q. robur, A. glutinosa, L. decidua</i>
, and
<i>P. abies</i>
barks exhibit particularly high activities on most bioassays, suggesting their promising use as active ingredients in the dermo-cosmetic industry.</div>
</front>
</TEI>
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<MedlineCitation Status="MEDLINE" Owner="NLM">
<PMID Version="1">27352384</PMID>
<DateCompleted>
<Year>2017</Year>
<Month>03</Month>
<Day>27</Day>
</DateCompleted>
<DateRevised>
<Year>2017</Year>
<Month>03</Month>
<Day>27</Day>
</DateRevised>
<Article PubModel="Print-Electronic">
<Journal>
<ISSN IssnType="Electronic">1439-0221</ISSN>
<JournalIssue CitedMedium="Internet">
<Volume>82</Volume>
<Issue>15</Issue>
<PubDate>
<Year>2016</Year>
<Month>Oct</Month>
</PubDate>
</JournalIssue>
<Title>Planta medica</Title>
<ISOAbbreviation>Planta Med</ISOAbbreviation>
</Journal>
<ArticleTitle>In Vitro Dermo-Cosmetic Evaluation of Bark Extracts from Common Temperate Trees.</ArticleTitle>
<Pagination>
<MedlinePgn>1351-1358</MedlinePgn>
</Pagination>
<Abstract>
<AbstractText>Wood residues produced from forestry activities represent an interesting source of biologically active, high value-added secondary metabolites. In this study, 30 extracts from 10 barks of deciduous and coniferous tree species were investigated for their potential dermo-cosmetic use. The extracts were obtained from
<i>Fagus sylvatica, Quercus robur, Alnus glutinosa, Prunus avium, Acer pseudoplatanus, Fraxinus excelsior, Populus robusta, Larix decidua, Picea abies</i>
, and
<i>Populus tremula</i>
after three successive solid/liquid extractions of the barks with
<i>n-</i>
heptane, methanol, and methanol/water. All extracts were evaluated for their radical scavenging capacity, for their elastase, collagenase, and tyrosinase inhibitory activities, as well as for their antibacterial activity against gram-positive
<i>Staphylococcus aureus</i>
. In parallel, the global metabolite profiles of all extracts were established by 1D and 2D NMR and related to their biological activity. The results showed that the methanol extracts of
<i>Q. robur, A. glutinosa, L. decidua</i>
, and
<i>P. abies</i>
barks exhibit particularly high activities on most bioassays, suggesting their promising use as active ingredients in the dermo-cosmetic industry.</AbstractText>
<CopyrightInformation>Georg Thieme Verlag KG Stuttgart · New York.</CopyrightInformation>
</Abstract>
<AuthorList CompleteYN="Y">
<Author ValidYN="Y">
<LastName>Hubert</LastName>
<ForeName>Jane</ForeName>
<Initials>J</Initials>
<AffiliationInfo>
<Affiliation>Institut de Chimie Moléculaire de Reims, UMR CNRS 7312, SFR CAP'SANTE, UFR de Pharmacie, Université de Reims Champagne-Ardenne, Reims, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Angelis</LastName>
<ForeName>Apostolis</ForeName>
<Initials>A</Initials>
<AffiliationInfo>
<Affiliation>Institut de Chimie Moléculaire de Reims, UMR CNRS 7312, SFR CAP'SANTE, UFR de Pharmacie, Université de Reims Champagne-Ardenne, Reims, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Aligiannis</LastName>
<ForeName>Nektarios</ForeName>
<Initials>N</Initials>
<AffiliationInfo>
<Affiliation>Division of Pharmacognosy and Natural Products Chemistry, School of Pharmacy, University of Athens, Panepistimioupolis, Zographou, Athens, Greece.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Rosalia</LastName>
<ForeName>Michalea</ForeName>
<Initials>M</Initials>
<AffiliationInfo>
<Affiliation>Division of Pharmacognosy and Natural Products Chemistry, School of Pharmacy, University of Athens, Panepistimioupolis, Zographou, Athens, Greece.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Abedini</LastName>
<ForeName>Amin</ForeName>
<Initials>A</Initials>
<AffiliationInfo>
<Affiliation>Institut de Chimie Moléculaire de Reims, UMR CNRS 7312, SFR CAP'SANTE, UFR de Pharmacie, Université de Reims Champagne-Ardenne, Reims, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Bakiri</LastName>
<ForeName>Ali</ForeName>
<Initials>A</Initials>
<AffiliationInfo>
<Affiliation>Institut de Chimie Moléculaire de Reims, UMR CNRS 7312, SFR CAP'SANTE, UFR de Pharmacie, Université de Reims Champagne-Ardenne, Reims, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Reynaud</LastName>
<ForeName>Romain</ForeName>
<Initials>R</Initials>
<AffiliationInfo>
<Affiliation>Soliance-Givaudan, Pomacle, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Nuzillard</LastName>
<ForeName>Jean-Marc</ForeName>
<Initials>JM</Initials>
<AffiliationInfo>
<Affiliation>Institut de Chimie Moléculaire de Reims, UMR CNRS 7312, SFR CAP'SANTE, UFR de Pharmacie, Université de Reims Champagne-Ardenne, Reims, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Gangloff</LastName>
<ForeName>Sophie C</ForeName>
<Initials>SC</Initials>
<AffiliationInfo>
<Affiliation>Biomatériaux et Inflammation en Site Osseux, EA 4691, SFR CAP-Santé, UFR de Pharmacie, Université de Reims Champagne Ardenne, Reims, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Skaltsounis</LastName>
<ForeName>Alexios-Leandros</ForeName>
<Initials>AL</Initials>
<AffiliationInfo>
<Affiliation>Division of Pharmacognosy and Natural Products Chemistry, School of Pharmacy, University of Athens, Panepistimioupolis, Zographou, Athens, Greece.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Renault</LastName>
<ForeName>Jean-Hugues</ForeName>
<Initials>JH</Initials>
<AffiliationInfo>
<Affiliation>Institut de Chimie Moléculaire de Reims, UMR CNRS 7312, SFR CAP'SANTE, UFR de Pharmacie, Université de Reims Champagne-Ardenne, Reims, France.</Affiliation>
</AffiliationInfo>
</Author>
</AuthorList>
<Language>eng</Language>
<PublicationTypeList>
<PublicationType UI="D016428">Journal Article</PublicationType>
</PublicationTypeList>
<ArticleDate DateType="Electronic">
<Year>2016</Year>
<Month>06</Month>
<Day>28</Day>
</ArticleDate>
</Article>
<MedlineJournalInfo>
<Country>Germany</Country>
<MedlineTA>Planta Med</MedlineTA>
<NlmUniqueID>0066751</NlmUniqueID>
<ISSNLinking>0032-0943</ISSNLinking>
</MedlineJournalInfo>
<ChemicalList>
<Chemical>
<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D000900">Anti-Bacterial Agents</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D003879">Dermatologic Agents</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D004791">Enzyme Inhibitors</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D010936">Plant Extracts</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>EC 1.14.18.1</RegistryNumber>
<NameOfSubstance UI="D014442">Monophenol Monooxygenase</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>EC 3.4.21.36</RegistryNumber>
<NameOfSubstance UI="D010196">Pancreatic Elastase</NameOfSubstance>
</Chemical>
</ChemicalList>
<CitationSubset>IM</CitationSubset>
<MeshHeadingList>
<MeshHeading>
<DescriptorName UI="D000818" MajorTopicYN="N">Animals</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D000900" MajorTopicYN="N">Anti-Bacterial Agents</DescriptorName>
<QualifierName UI="Q000494" MajorTopicYN="N">pharmacology</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D003879" MajorTopicYN="N">Dermatologic Agents</DescriptorName>
<QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName>
<QualifierName UI="Q000494" MajorTopicYN="Y">pharmacology</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D004353" MajorTopicYN="N">Drug Evaluation, Preclinical</DescriptorName>
<QualifierName UI="Q000379" MajorTopicYN="N">methods</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D004791" MajorTopicYN="N">Enzyme Inhibitors</DescriptorName>
<QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName>
<QualifierName UI="Q000494" MajorTopicYN="N">pharmacology</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D009682" MajorTopicYN="N">Magnetic Resonance Spectroscopy</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D014442" MajorTopicYN="N">Monophenol Monooxygenase</DescriptorName>
<QualifierName UI="Q000037" MajorTopicYN="N">antagonists & inhibitors</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D010196" MajorTopicYN="N">Pancreatic Elastase</DescriptorName>
<QualifierName UI="Q000037" MajorTopicYN="N">antagonists & inhibitors</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D024301" MajorTopicYN="N">Plant Bark</DescriptorName>
<QualifierName UI="Q000737" MajorTopicYN="Y">chemistry</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D010936" MajorTopicYN="N">Plant Extracts</DescriptorName>
<QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName>
<QualifierName UI="Q000494" MajorTopicYN="Y">pharmacology</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D013211" MajorTopicYN="N">Staphylococcus aureus</DescriptorName>
<QualifierName UI="Q000187" MajorTopicYN="N">drug effects</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D014197" MajorTopicYN="N">Trees</DescriptorName>
<QualifierName UI="Q000737" MajorTopicYN="Y">chemistry</QualifierName>
</MeshHeading>
</MeshHeadingList>
</MedlineCitation>
<PubmedData>
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<Year>2016</Year>
<Month>6</Month>
<Day>29</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="medline">
<Year>2017</Year>
<Month>3</Month>
<Day>28</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="entrez">
<Year>2016</Year>
<Month>6</Month>
<Day>29</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
</History>
<PublicationStatus>ppublish</PublicationStatus>
<ArticleIdList>
<ArticleId IdType="pubmed">27352384</ArticleId>
<ArticleId IdType="doi">10.1055/s-0042-110180</ArticleId>
</ArticleIdList>
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</pubmed>
<affiliations>
<list>
<country>
<li>France</li>
<li>Grèce</li>
</country>
<region>
<li>Attique (région)</li>
<li>Champagne-Ardenne</li>
<li>Grand Est</li>
</region>
<settlement>
<li>Athènes</li>
<li>Reims</li>
</settlement>
<orgName>
<li>Université de Reims Champagne-Ardenne</li>
</orgName>
</list>
<tree>
<country name="France">
<region name="Grand Est">
<name sortKey="Hubert, Jane" sort="Hubert, Jane" uniqKey="Hubert J" first="Jane" last="Hubert">Jane Hubert</name>
</region>
<name sortKey="Abedini, Amin" sort="Abedini, Amin" uniqKey="Abedini A" first="Amin" last="Abedini">Amin Abedini</name>
<name sortKey="Angelis, Apostolis" sort="Angelis, Apostolis" uniqKey="Angelis A" first="Apostolis" last="Angelis">Apostolis Angelis</name>
<name sortKey="Bakiri, Ali" sort="Bakiri, Ali" uniqKey="Bakiri A" first="Ali" last="Bakiri">Ali Bakiri</name>
<name sortKey="Gangloff, Sophie C" sort="Gangloff, Sophie C" uniqKey="Gangloff S" first="Sophie C" last="Gangloff">Sophie C. Gangloff</name>
<name sortKey="Nuzillard, Jean Marc" sort="Nuzillard, Jean Marc" uniqKey="Nuzillard J" first="Jean-Marc" last="Nuzillard">Jean-Marc Nuzillard</name>
<name sortKey="Renault, Jean Hugues" sort="Renault, Jean Hugues" uniqKey="Renault J" first="Jean-Hugues" last="Renault">Jean-Hugues Renault</name>
<name sortKey="Reynaud, Romain" sort="Reynaud, Romain" uniqKey="Reynaud R" first="Romain" last="Reynaud">Romain Reynaud</name>
</country>
<country name="Grèce">
<region name="Attique (région)">
<name sortKey="Aligiannis, Nektarios" sort="Aligiannis, Nektarios" uniqKey="Aligiannis N" first="Nektarios" last="Aligiannis">Nektarios Aligiannis</name>
</region>
<name sortKey="Rosalia, Michalea" sort="Rosalia, Michalea" uniqKey="Rosalia M" first="Michalea" last="Rosalia">Michalea Rosalia</name>
<name sortKey="Skaltsounis, Alexios Leandros" sort="Skaltsounis, Alexios Leandros" uniqKey="Skaltsounis A" first="Alexios-Leandros" last="Skaltsounis">Alexios-Leandros Skaltsounis</name>
</country>
</tree>
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