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Investigation of the mechanism of action of Porana sinensis Hemsl. against gout arthritis using network pharmacology and experimental validation.

Identifieur interne : 000127 ( Main/Exploration ); précédent : 000126; suivant : 000128

Investigation of the mechanism of action of Porana sinensis Hemsl. against gout arthritis using network pharmacology and experimental validation.

Auteurs : Xia Du [République populaire de Chine] ; Lintao Zhao [République populaire de Chine] ; Yuanyuan Yang [République populaire de Chine] ; Zijia Zhang [République populaire de Chine] ; Jing Hu [République populaire de Chine] ; Hui Ren [République populaire de Chine] ; Zhiyong Chen [République populaire de Chine] ; Ye Li [République populaire de Chine]

Source :

RBID : pubmed:31988013

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English descriptors

Abstract

ETHNOPHARMACOLOGICAL RELEVANCE

Porana sinensis Hemsl. has been widely used to treat joint pain and rheumatoid arthritis in traditional Chinese medicine (TCM). Although evidence exists to support a pharmacological action of P. sinensis for the treatment of gout arthritis (GA), the underlying mechanism of action remains unknown due to it being a multi-component and multi-target agent.

AIM OF THE STUDY

To clarify the active compounds and mechanism of P. sinensis against GA.

MATERIALS AND METHODS

The present study combined network pharmacology with experiments to clarify the mechanism of P. sinensis against GA. A protein-protein interaction network for gout was constructed to identify the potential drug targets, and molecular docking was subsequently performed to determine whether the protein was a target for the compounds of P. sinensis. KEGG pathway analysis was then conducted to elucidate the pathway involved in the P. sinensis-mediated treatment of gout. A rat model of GA was used to further investigate the mechanism of P. sinensis against GA.

RESULTS

The network pharmacology study indicates that coumarins and chlorogenic acids of P. sinensis may serve as additives to GA treatment. P. sinensis played a role in the treatment of GA by regulating the PI3K-Akt, MAPK, NF-kappa B and toll-like receptor pathways and so on. Moreover, experimental validation suggests that P. sinensis extract significantly suppressed the expression of TLR2 and MyD88 mRNA, regulating the release of cytokines (IL-1β, IL-4 and TGF-β), lowering lipid peroxidation (MDA) and increasing antioxidant status (SOD).

CONCLUSION

The present study clarifies the mechanism of P. sinensis against GA, and provides evidence to support its clinical use.


DOI: 10.1016/j.jep.2020.112606
PubMed: 31988013


Affiliations:


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<term>Arthritis, Gouty (genetics)</term>
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<term>Extraits de plantes (usage thérapeutique)</term>
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<term>Goutte articulaire (traitement médicamenteux)</term>
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<term>Coumarines</term>
<term>Extraits de plantes</term>
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<term>Cytokines</term>
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<term>Cartes d'interactions protéiques</term>
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<p>
<b>ETHNOPHARMACOLOGICAL RELEVANCE</b>
</p>
<p>Porana sinensis Hemsl. has been widely used to treat joint pain and rheumatoid arthritis in traditional Chinese medicine (TCM). Although evidence exists to support a pharmacological action of P. sinensis for the treatment of gout arthritis (GA), the underlying mechanism of action remains unknown due to it being a multi-component and multi-target agent.</p>
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<div type="abstract" xml:lang="en">
<p>
<b>AIM OF THE STUDY</b>
</p>
<p>To clarify the active compounds and mechanism of P. sinensis against GA.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>MATERIALS AND METHODS</b>
</p>
<p>The present study combined network pharmacology with experiments to clarify the mechanism of P. sinensis against GA. A protein-protein interaction network for gout was constructed to identify the potential drug targets, and molecular docking was subsequently performed to determine whether the protein was a target for the compounds of P. sinensis. KEGG pathway analysis was then conducted to elucidate the pathway involved in the P. sinensis-mediated treatment of gout. A rat model of GA was used to further investigate the mechanism of P. sinensis against GA.</p>
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<div type="abstract" xml:lang="en">
<p>
<b>RESULTS</b>
</p>
<p>The network pharmacology study indicates that coumarins and chlorogenic acids of P. sinensis may serve as additives to GA treatment. P. sinensis played a role in the treatment of GA by regulating the PI3K-Akt, MAPK, NF-kappa B and toll-like receptor pathways and so on. Moreover, experimental validation suggests that P. sinensis extract significantly suppressed the expression of TLR2 and MyD88 mRNA, regulating the release of cytokines (IL-1β, IL-4 and TGF-β), lowering lipid peroxidation (MDA) and increasing antioxidant status (SOD).</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>CONCLUSION</b>
</p>
<p>The present study clarifies the mechanism of P. sinensis against GA, and provides evidence to support its clinical use.</p>
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<AbstractText Label="ETHNOPHARMACOLOGICAL RELEVANCE" NlmCategory="BACKGROUND">Porana sinensis Hemsl. has been widely used to treat joint pain and rheumatoid arthritis in traditional Chinese medicine (TCM). Although evidence exists to support a pharmacological action of P. sinensis for the treatment of gout arthritis (GA), the underlying mechanism of action remains unknown due to it being a multi-component and multi-target agent.</AbstractText>
<AbstractText Label="AIM OF THE STUDY" NlmCategory="OBJECTIVE">To clarify the active compounds and mechanism of P. sinensis against GA.</AbstractText>
<AbstractText Label="MATERIALS AND METHODS" NlmCategory="METHODS">The present study combined network pharmacology with experiments to clarify the mechanism of P. sinensis against GA. A protein-protein interaction network for gout was constructed to identify the potential drug targets, and molecular docking was subsequently performed to determine whether the protein was a target for the compounds of P. sinensis. KEGG pathway analysis was then conducted to elucidate the pathway involved in the P. sinensis-mediated treatment of gout. A rat model of GA was used to further investigate the mechanism of P. sinensis against GA.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">The network pharmacology study indicates that coumarins and chlorogenic acids of P. sinensis may serve as additives to GA treatment. P. sinensis played a role in the treatment of GA by regulating the PI3K-Akt, MAPK, NF-kappa B and toll-like receptor pathways and so on. Moreover, experimental validation suggests that P. sinensis extract significantly suppressed the expression of TLR2 and MyD88 mRNA, regulating the release of cytokines (IL-1β, IL-4 and TGF-β), lowering lipid peroxidation (MDA) and increasing antioxidant status (SOD).</AbstractText>
<AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">The present study clarifies the mechanism of P. sinensis against GA, and provides evidence to support its clinical use.</AbstractText>
<CopyrightInformation>Copyright © 2020 Elsevier B.V. All rights reserved.</CopyrightInformation>
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<DescriptorName UI="D000818" MajorTopicYN="N">Animals</DescriptorName>
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<DescriptorName UI="D000843" MajorTopicYN="N">Ankle Joint</DescriptorName>
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<QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName>
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<DescriptorName UI="D015210" MajorTopicYN="N">Arthritis, Gouty</DescriptorName>
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<QualifierName UI="Q000627" MajorTopicYN="N">therapeutic use</QualifierName>
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<MeshHeading>
<DescriptorName UI="D060066" MajorTopicYN="N">Protein Interaction Maps</DescriptorName>
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<Keyword MajorTopicYN="N">Anti-inflammatory</Keyword>
<Keyword MajorTopicYN="N">Experimental validation</Keyword>
<Keyword MajorTopicYN="N">Gout arthritis</Keyword>
<Keyword MajorTopicYN="N">Network pharmacology</Keyword>
<Keyword MajorTopicYN="N">Porana sinensis</Keyword>
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<Month>11</Month>
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<PubMedPubDate PubStatus="revised">
<Year>2020</Year>
<Month>01</Month>
<Day>20</Day>
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<ArticleId IdType="pii">S0378-8741(19)34439-3</ArticleId>
<ArticleId IdType="doi">10.1016/j.jep.2020.112606</ArticleId>
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<li>République populaire de Chine</li>
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<name sortKey="Du, Xia" sort="Du, Xia" uniqKey="Du X" first="Xia" last="Du">Xia Du</name>
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<name sortKey="Chen, Zhiyong" sort="Chen, Zhiyong" uniqKey="Chen Z" first="Zhiyong" last="Chen">Zhiyong Chen</name>
<name sortKey="Hu, Jing" sort="Hu, Jing" uniqKey="Hu J" first="Jing" last="Hu">Jing Hu</name>
<name sortKey="Li, Ye" sort="Li, Ye" uniqKey="Li Y" first="Ye" last="Li">Ye Li</name>
<name sortKey="Ren, Hui" sort="Ren, Hui" uniqKey="Ren H" first="Hui" last="Ren">Hui Ren</name>
<name sortKey="Yang, Yuanyuan" sort="Yang, Yuanyuan" uniqKey="Yang Y" first="Yuanyuan" last="Yang">Yuanyuan Yang</name>
<name sortKey="Zhang, Zijia" sort="Zhang, Zijia" uniqKey="Zhang Z" first="Zijia" last="Zhang">Zijia Zhang</name>
<name sortKey="Zhao, Lintao" sort="Zhao, Lintao" uniqKey="Zhao L" first="Lintao" last="Zhao">Lintao Zhao</name>
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