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Anti-inflammatory effects of ethanol extracts of Chinese propolis and buds from poplar (Populus×canadensis).

Identifieur interne : 002366 ( Main/Exploration ); précédent : 002365; suivant : 002367

Anti-inflammatory effects of ethanol extracts of Chinese propolis and buds from poplar (Populus×canadensis).

Auteurs : Kai Wang [République populaire de Chine] ; Jianglin Zhang [République populaire de Chine] ; Shun Ping [République populaire de Chine] ; Quanxin Ma [République populaire de Chine] ; Xuan Chen [République populaire de Chine] ; Hongzhuan Xuan [République populaire de Chine] ; Jinhu Shi [République populaire de Chine] ; Cuiping Zhang [République populaire de Chine] ; Fuliang Hu [République populaire de Chine]

Source :

RBID : pubmed:24882729

Descripteurs français

English descriptors

Abstract

ETHNOPHARMACOLOGICAL RELEVANCE

Propolis is used widely in a number of cultures as a folk medicine and is gaining wider recognition for its potential therapeutic use, due to its wide range of biological properties and pharmacological activities, especially its anti-inflammatory effects. Despite an increasing number of studies focused on the biological activities of propolis together with its botanical sources, studies on Chinese propolis are insufficient. This study was designed to investigate the anti-inflammatory properties of ethanol extracts from Chinese propolis (EECP) and poplar buds (EEPB) from Populus×canadensis Moench (Salicaceae family).

MATERIALS AND METHODS

Phytochemical analysis of EECP and EEPB was performed via total phenolic and flavonoid content measurements followed by high-performance liquid chromatography (HPLC) analysis. DPPH and ABTS free-radical scavenging methods were used to evaluate their anti-oxidant properties. The anti-inflammatory effects of EECP and EEPB were investigated in vitro by evaluating their modulating effects on the key inflammatory cytokines and mediators in LPS/IFN-γ co-stimulated RAW 264.7 cells and by measuring nuclear factor (NF)-κB activation in TNF-α or IL-1β stimulation HEK 293 cells using reporter gene assays. Their effects on acute inflammatory symptoms (LPS-induced endotoxemia and acute pulmonary damage) were also examined in mice.

RESULTS

EECP and EEPB exhibited strong free-radical scavenging activity and significant in vitro anti-inflammatory effects by modulating key inflammatory mediators of mRNA transcription, inhibiting the production of specific inflammatory cytokines, and blocking the activation of nuclear factor (NF)-κB. The administration of EECP and EEPB (25 and 100 mg/kg) provided significant protective effects by attenuating lung histopathological changes and suppressing the secretion of LPS-stimulated inflammatory cytokines, such as interleukin-6 (IL-6), IL-10, MCP-1, TNF-α and IL-12p70 production in endotoxemic mice.

CONCLUSIONS

The results presented here reveal the potent anti-inflammatory properties of Chinese propolis and poplar buds, and provide biological information for developing suitable substitute(s) for propolis in the prevention and treatment of inflammatory diseases.


DOI: 10.1016/j.jep.2014.05.037
PubMed: 24882729


Affiliations:


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Le document en format XML

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<term>Mice, Inbred ICR</term>
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<keywords scheme="MESH" xml:lang="fr">
<term>Animaux</term>
<term>Cellules HEK293</term>
<term>Chine</term>
<term>Humains</term>
<term>Lignée cellulaire</term>
<term>Mâle</term>
<term>Relation dose-effet des médicaments</term>
<term>Souris</term>
<term>Souris de lignée ICR</term>
</keywords>
<keywords scheme="Wicri" type="geographic" xml:lang="fr">
<term>République populaire de Chine</term>
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<front>
<div type="abstract" xml:lang="en">
<p>
<b>ETHNOPHARMACOLOGICAL RELEVANCE</b>
</p>
<p>Propolis is used widely in a number of cultures as a folk medicine and is gaining wider recognition for its potential therapeutic use, due to its wide range of biological properties and pharmacological activities, especially its anti-inflammatory effects. Despite an increasing number of studies focused on the biological activities of propolis together with its botanical sources, studies on Chinese propolis are insufficient. This study was designed to investigate the anti-inflammatory properties of ethanol extracts from Chinese propolis (EECP) and poplar buds (EEPB) from Populus×canadensis Moench (Salicaceae family).</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>MATERIALS AND METHODS</b>
</p>
<p>Phytochemical analysis of EECP and EEPB was performed via total phenolic and flavonoid content measurements followed by high-performance liquid chromatography (HPLC) analysis. DPPH and ABTS free-radical scavenging methods were used to evaluate their anti-oxidant properties. The anti-inflammatory effects of EECP and EEPB were investigated in vitro by evaluating their modulating effects on the key inflammatory cytokines and mediators in LPS/IFN-γ co-stimulated RAW 264.7 cells and by measuring nuclear factor (NF)-κB activation in TNF-α or IL-1β stimulation HEK 293 cells using reporter gene assays. Their effects on acute inflammatory symptoms (LPS-induced endotoxemia and acute pulmonary damage) were also examined in mice.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>RESULTS</b>
</p>
<p>EECP and EEPB exhibited strong free-radical scavenging activity and significant in vitro anti-inflammatory effects by modulating key inflammatory mediators of mRNA transcription, inhibiting the production of specific inflammatory cytokines, and blocking the activation of nuclear factor (NF)-κB. The administration of EECP and EEPB (25 and 100 mg/kg) provided significant protective effects by attenuating lung histopathological changes and suppressing the secretion of LPS-stimulated inflammatory cytokines, such as interleukin-6 (IL-6), IL-10, MCP-1, TNF-α and IL-12p70 production in endotoxemic mice.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>CONCLUSIONS</b>
</p>
<p>The results presented here reveal the potent anti-inflammatory properties of Chinese propolis and poplar buds, and provide biological information for developing suitable substitute(s) for propolis in the prevention and treatment of inflammatory diseases.</p>
</div>
</front>
</TEI>
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<Year>2015</Year>
<Month>04</Month>
<Day>07</Day>
</DateCompleted>
<DateRevised>
<Year>2014</Year>
<Month>07</Month>
<Day>28</Day>
</DateRevised>
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<ISSN IssnType="Electronic">1872-7573</ISSN>
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<Volume>155</Volume>
<Issue>1</Issue>
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<Year>2014</Year>
<Month>Aug</Month>
<Day>08</Day>
</PubDate>
</JournalIssue>
<Title>Journal of ethnopharmacology</Title>
<ISOAbbreviation>J Ethnopharmacol</ISOAbbreviation>
</Journal>
<ArticleTitle>Anti-inflammatory effects of ethanol extracts of Chinese propolis and buds from poplar (Populus×canadensis).</ArticleTitle>
<Pagination>
<MedlinePgn>300-11</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1016/j.jep.2014.05.037</ELocationID>
<ELocationID EIdType="pii" ValidYN="Y">S0378-8741(14)00406-1</ELocationID>
<Abstract>
<AbstractText Label="ETHNOPHARMACOLOGICAL RELEVANCE" NlmCategory="BACKGROUND">Propolis is used widely in a number of cultures as a folk medicine and is gaining wider recognition for its potential therapeutic use, due to its wide range of biological properties and pharmacological activities, especially its anti-inflammatory effects. Despite an increasing number of studies focused on the biological activities of propolis together with its botanical sources, studies on Chinese propolis are insufficient. This study was designed to investigate the anti-inflammatory properties of ethanol extracts from Chinese propolis (EECP) and poplar buds (EEPB) from Populus×canadensis Moench (Salicaceae family).</AbstractText>
<AbstractText Label="MATERIALS AND METHODS" NlmCategory="METHODS">Phytochemical analysis of EECP and EEPB was performed via total phenolic and flavonoid content measurements followed by high-performance liquid chromatography (HPLC) analysis. DPPH and ABTS free-radical scavenging methods were used to evaluate their anti-oxidant properties. The anti-inflammatory effects of EECP and EEPB were investigated in vitro by evaluating their modulating effects on the key inflammatory cytokines and mediators in LPS/IFN-γ co-stimulated RAW 264.7 cells and by measuring nuclear factor (NF)-κB activation in TNF-α or IL-1β stimulation HEK 293 cells using reporter gene assays. Their effects on acute inflammatory symptoms (LPS-induced endotoxemia and acute pulmonary damage) were also examined in mice.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">EECP and EEPB exhibited strong free-radical scavenging activity and significant in vitro anti-inflammatory effects by modulating key inflammatory mediators of mRNA transcription, inhibiting the production of specific inflammatory cytokines, and blocking the activation of nuclear factor (NF)-κB. The administration of EECP and EEPB (25 and 100 mg/kg) provided significant protective effects by attenuating lung histopathological changes and suppressing the secretion of LPS-stimulated inflammatory cytokines, such as interleukin-6 (IL-6), IL-10, MCP-1, TNF-α and IL-12p70 production in endotoxemic mice.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">The results presented here reveal the potent anti-inflammatory properties of Chinese propolis and poplar buds, and provide biological information for developing suitable substitute(s) for propolis in the prevention and treatment of inflammatory diseases.</AbstractText>
<CopyrightInformation>Copyright © 2014 Elsevier Ireland Ltd. All rights reserved.</CopyrightInformation>
</Abstract>
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<Author ValidYN="Y">
<LastName>Wang</LastName>
<ForeName>Kai</ForeName>
<Initials>K</Initials>
<AffiliationInfo>
<Affiliation>College of Animal Sciences, Zhejiang University, Hangzhou 310058, China.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Zhang</LastName>
<ForeName>Jianglin</ForeName>
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<Affiliation>College of Animal Sciences, Zhejiang University, Hangzhou 310058, China.</Affiliation>
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<LastName>Ping</LastName>
<ForeName>Shun</ForeName>
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<AffiliationInfo>
<Affiliation>College of Animal Sciences, Zhejiang University, Hangzhou 310058, China.</Affiliation>
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</Author>
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<LastName>Ma</LastName>
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<AffiliationInfo>
<Affiliation>Laboratory Animal Research Center, Zhejiang Chinese Medical University, Hangzhou 310053, China.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Chen</LastName>
<ForeName>Xuan</ForeName>
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<AffiliationInfo>
<Affiliation>Zhejiang Academy of Traditional Chinese Medicine, Hangzhou 310007, China.</Affiliation>
</AffiliationInfo>
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<ForeName>Hongzhuan</ForeName>
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<AffiliationInfo>
<Affiliation>School of Life Science, Liaocheng University, Liaocheng 252059, China.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Shi</LastName>
<ForeName>Jinhu</ForeName>
<Initials>J</Initials>
<AffiliationInfo>
<Affiliation>College of Animal Sciences, Zhejiang University, Hangzhou 310058, China; Husbandry and veterinary technical popularization center of Zhejiang Province, Hangzhou 310020, China.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Zhang</LastName>
<ForeName>Cuiping</ForeName>
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<Affiliation>College of Animal Sciences, Zhejiang University, Hangzhou 310058, China.</Affiliation>
</AffiliationInfo>
</Author>
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<AffiliationInfo>
<Affiliation>College of Animal Sciences, Zhejiang University, Hangzhou 310058, China. Electronic address: flhu@zju.edu.cn.</Affiliation>
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<Day>02</Day>
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<Country>Ireland</Country>
<MedlineTA>J Ethnopharmacol</MedlineTA>
<NlmUniqueID>7903310</NlmUniqueID>
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<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D000893">Anti-Inflammatory Agents</NameOfSubstance>
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<Chemical>
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<CitationSubset>IM</CitationSubset>
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<MeshHeading>
<DescriptorName UI="D000818" MajorTopicYN="N">Animals</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D000893" MajorTopicYN="N">Anti-Inflammatory Agents</DescriptorName>
<QualifierName UI="Q000008" MajorTopicYN="N">administration & dosage</QualifierName>
<QualifierName UI="Q000302" MajorTopicYN="N">isolation & purification</QualifierName>
<QualifierName UI="Q000494" MajorTopicYN="Y">pharmacology</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D002460" MajorTopicYN="N">Cell Line</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D002681" MajorTopicYN="N" Type="Geographic">China</DescriptorName>
</MeshHeading>
<MeshHeading>
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<QualifierName UI="Q000379" MajorTopicYN="N">methods</QualifierName>
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<MeshHeading>
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<MeshHeading>
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<MeshHeading>
<DescriptorName UI="D000431" MajorTopicYN="N">Ethanol</DescriptorName>
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<MeshHeading>
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<MeshHeading>
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<MeshHeading>
<DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName>
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<MeshHeading>
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<MeshHeading>
<DescriptorName UI="D032107" MajorTopicYN="N">Populus</DescriptorName>
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<name sortKey="Ma, Quanxin" sort="Ma, Quanxin" uniqKey="Ma Q" first="Quanxin" last="Ma">Quanxin Ma</name>
<name sortKey="Ping, Shun" sort="Ping, Shun" uniqKey="Ping S" first="Shun" last="Ping">Shun Ping</name>
<name sortKey="Shi, Jinhu" sort="Shi, Jinhu" uniqKey="Shi J" first="Jinhu" last="Shi">Jinhu Shi</name>
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