Anti-inflammatory activity of flavonoids from Populus davidiana.
Identifieur interne : 003C41 ( Main/Curation ); précédent : 003C40; suivant : 003C42Anti-inflammatory activity of flavonoids from Populus davidiana.
Auteurs : Xinfeng Zhang [Corée du Sud] ; Tran Manh Hung ; Phuong Thien Phuong ; Tran Minh Ngoc ; Byung-Sun Min ; Kyung-Sik Song ; Yeon Hee Seong ; Kihwan BaeSource :
- Archives of pharmacal research [ 0253-6269 ] ; 2006.
Descripteurs français
- KwdFr :
- Anti-inflammatoires non stéroïdiens (isolement et purification), Anti-inflammatoires non stéroïdiens (pharmacologie), Antienzymes (pharmacologie), Cyclooxygenase 1 (métabolisme), Extraits de plantes (analyse), Flavonoïdes (isolement et purification), Flavonoïdes (pharmacologie), Hydrolyse (MeSH), Inhibiteurs de la cyclooxygénase 2 (isolement et purification), Inhibiteurs de la cyclooxygénase 2 (pharmacologie), Inhibiteurs des cyclooxygénases (isolement et purification), Inhibiteurs des cyclooxygénases (pharmacologie), Populus (composition chimique), Spectrophotométrie IR (MeSH), Spectrophotométrie UV (MeSH), Spectroscopie par résonance magnétique (MeSH), Superoxydes (métabolisme), Xanthine oxidase (antagonistes et inhibiteurs), Écorce (composition chimique).
- MESH :
- analyse : Extraits de plantes.
- antagonistes et inhibiteurs : Xanthine oxidase.
- composition chimique : Populus, Écorce.
- isolement et purification : Anti-inflammatoires non stéroïdiens, Flavonoïdes, Inhibiteurs de la cyclooxygénase 2, Inhibiteurs des cyclooxygénases.
- métabolisme : Cyclooxygenase 1, Superoxydes.
- pharmacologie : Anti-inflammatoires non stéroïdiens, Antienzymes, Flavonoïdes, Inhibiteurs de la cyclooxygénase 2, Inhibiteurs des cyclooxygénases.
- Hydrolyse, Spectrophotométrie IR, Spectrophotométrie UV, Spectroscopie par résonance magnétique.
English descriptors
- KwdEn :
- Anti-Inflammatory Agents, Non-Steroidal (isolation & purification), Anti-Inflammatory Agents, Non-Steroidal (pharmacology), Cyclooxygenase 1 (metabolism), Cyclooxygenase 2 Inhibitors (isolation & purification), Cyclooxygenase 2 Inhibitors (pharmacology), Cyclooxygenase Inhibitors (isolation & purification), Cyclooxygenase Inhibitors (pharmacology), Enzyme Inhibitors (pharmacology), Flavonoids (isolation & purification), Flavonoids (pharmacology), Hydrolysis (MeSH), Magnetic Resonance Spectroscopy (MeSH), Plant Bark (chemistry), Plant Extracts (analysis), Populus (chemistry), Spectrophotometry, Infrared (MeSH), Spectrophotometry, Ultraviolet (MeSH), Superoxides (metabolism), Xanthine Oxidase (antagonists & inhibitors).
- MESH :
- chemical , analysis : Plant Extracts.
- chemical , antagonists & inhibitors : Xanthine Oxidase.
- chemical , isolation & purification : Anti-Inflammatory Agents, Non-Steroidal, Cyclooxygenase 2 Inhibitors, Cyclooxygenase Inhibitors, Flavonoids.
- chemical , metabolism : Cyclooxygenase 1, Superoxides.
- chemical , pharmacology : Anti-Inflammatory Agents, Non-Steroidal, Cyclooxygenase 2 Inhibitors, Cyclooxygenase Inhibitors, Enzyme Inhibitors, Flavonoids.
- chemistry : Plant Bark, Populus.
- Hydrolysis, Magnetic Resonance Spectroscopy, Spectrophotometry, Infrared, Spectrophotometry, Ultraviolet.
Abstract
An in vitro bioassay-guide revealed that the methanol (MeOH) extract of the stem bark of Populus davidiana showed considerable inhibitory activity against cyclooxygenase (COX-1, COX-2). Continuous phytochemical study of the MeOH extract of this plant led to the isolation of ten flavonoids; sakuranetin (1), rhamnocitrin (2), 7-O-methylaromadendrin (3), naringenin (4), eriodictyol (5), aromadendrin (6), kaempferol (7), neosakuranin (8), sakuranin (9) and sakurenetin-5,4'-di-beta-D-glucopyranoside (10). Their structures were identified on the basis of their physicochemical and spectroscopic analyses. The isolated compounds, 1-10, were tested for their inhibitory activities against COX-1 and COX-2. Compound 7 was found to have potent inhibitory effect on COX-1 and a moderate effect on COX-2, meanwhile, compounds 1-6 showed moderate inhibition against COX-1 only. Moreover, compounds 5-8 exhibited suppressive effects on xanthine oxidase (XO). These results may explain, in part, the traditional uses of P. davidiana in ethnomedicine.
DOI: 10.1007/BF02969299
PubMed: 17225458
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Ngoc</name></author><author><name sortKey="Min, Byung Sun" sort="Min, Byung Sun" uniqKey="Min B" first="Byung-Sun" last="Min">Byung-Sun Min</name></author><author><name sortKey="Song, Kyung Sik" sort="Song, Kyung Sik" uniqKey="Song K" first="Kyung-Sik" last="Song">Kyung-Sik Song</name></author><author><name sortKey="Seong, Yeon Hee" sort="Seong, Yeon Hee" uniqKey="Seong Y" first="Yeon Hee" last="Seong">Yeon Hee Seong</name></author><author><name sortKey="Bae, Kihwan" sort="Bae, Kihwan" uniqKey="Bae K" first="Kihwan" last="Bae">Kihwan Bae</name></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2006">2006</date><idno type="RBID">pubmed:17225458</idno><idno type="pmid">17225458</idno><idno type="doi">10.1007/BF02969299</idno><idno type="wicri:Area/Main/Corpus">003C41</idno><idno type="wicri:explorRef" wicri:stream="Main" wicri:step="Corpus" wicri:corpus="PubMed">003C41</idno><idno type="wicri:Area/Main/Curation">003C41</idno><idno 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purification)</term><term>Anti-inflammatoires non stéroïdiens (pharmacologie)</term><term>Antienzymes (pharmacologie)</term><term>Cyclooxygenase 1 (métabolisme)</term><term>Extraits de plantes (analyse)</term><term>Flavonoïdes (isolement et purification)</term><term>Flavonoïdes (pharmacologie)</term><term>Hydrolyse (MeSH)</term><term>Inhibiteurs de la cyclooxygénase 2 (isolement et purification)</term><term>Inhibiteurs de la cyclooxygénase 2 (pharmacologie)</term><term>Inhibiteurs des cyclooxygénases (isolement et purification)</term><term>Inhibiteurs des cyclooxygénases (pharmacologie)</term><term>Populus (composition chimique)</term><term>Spectrophotométrie IR (MeSH)</term><term>Spectrophotométrie UV (MeSH)</term><term>Spectroscopie par résonance magnétique (MeSH)</term><term>Superoxydes (métabolisme)</term><term>Xanthine oxidase (antagonistes et inhibiteurs)</term><term>Écorce (composition chimique)</term></keywords><keywords scheme="MESH" type="chemical" qualifier="analysis" xml:lang="en"><term>Plant Extracts</term></keywords><keywords scheme="MESH" type="chemical" qualifier="antagonists & inhibitors" xml:lang="en"><term>Xanthine Oxidase</term></keywords><keywords scheme="MESH" type="chemical" qualifier="isolation & purification" xml:lang="en"><term>Anti-Inflammatory Agents, Non-Steroidal</term><term>Cyclooxygenase 2 Inhibitors</term><term>Cyclooxygenase Inhibitors</term><term>Flavonoids</term></keywords><keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Cyclooxygenase 1</term><term>Superoxides</term></keywords><keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en"><term>Anti-Inflammatory Agents, Non-Steroidal</term><term>Cyclooxygenase 2 Inhibitors</term><term>Cyclooxygenase Inhibitors</term><term>Enzyme Inhibitors</term><term>Flavonoids</term></keywords><keywords scheme="MESH" qualifier="analyse" xml:lang="fr"><term>Extraits de plantes</term></keywords><keywords scheme="MESH" qualifier="antagonistes et inhibiteurs" xml:lang="fr"><term>Xanthine oxidase</term></keywords><keywords scheme="MESH" qualifier="chemistry" xml:lang="en"><term>Plant Bark</term><term>Populus</term></keywords><keywords scheme="MESH" qualifier="composition chimique" xml:lang="fr"><term>Populus</term><term>Écorce</term></keywords><keywords scheme="MESH" qualifier="isolement et purification" xml:lang="fr"><term>Anti-inflammatoires non stéroïdiens</term><term>Flavonoïdes</term><term>Inhibiteurs de la cyclooxygénase 2</term><term>Inhibiteurs des cyclooxygénases</term></keywords><keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>Cyclooxygenase 1</term><term>Superoxydes</term></keywords><keywords scheme="MESH" qualifier="pharmacologie" xml:lang="fr"><term>Anti-inflammatoires non stéroïdiens</term><term>Antienzymes</term><term>Flavonoïdes</term><term>Inhibiteurs de la cyclooxygénase 2</term><term>Inhibiteurs des cyclooxygénases</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Hydrolysis</term><term>Magnetic Resonance Spectroscopy</term><term>Spectrophotometry, Infrared</term><term>Spectrophotometry, Ultraviolet</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Hydrolyse</term><term>Spectrophotométrie IR</term><term>Spectrophotométrie UV</term><term>Spectroscopie par résonance magnétique</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">An in vitro bioassay-guide revealed that the methanol (MeOH) extract of the stem bark of Populus davidiana showed considerable inhibitory activity against cyclooxygenase (COX-1, COX-2). Continuous phytochemical study of the MeOH extract of this plant led to the isolation of ten flavonoids; sakuranetin (1), rhamnocitrin (2), 7-O-methylaromadendrin (3), naringenin (4), eriodictyol (5), aromadendrin (6), kaempferol (7), neosakuranin (8), sakuranin (9) and sakurenetin-5,4'-di-beta-D-glucopyranoside (10). Their structures were identified on the basis of their physicochemical and spectroscopic analyses. The isolated compounds, 1-10, were tested for their inhibitory activities against COX-1 and COX-2. Compound 7 was found to have potent inhibitory effect on COX-1 and a moderate effect on COX-2, meanwhile, compounds 1-6 showed moderate inhibition against COX-1 only. Moreover, compounds 5-8 exhibited suppressive effects on xanthine oxidase (XO). These results may explain, in part, the traditional uses of P. davidiana in ethnomedicine.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">17225458</PMID><DateCompleted><Year>2007</Year><Month>03</Month><Day>15</Day></DateCompleted><DateRevised><Year>2019</Year><Month>09</Month><Day>17</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Print">0253-6269</ISSN><JournalIssue CitedMedium="Print"><Volume>29</Volume><Issue>12</Issue><PubDate><Year>2006</Year><Month>Dec</Month></PubDate></JournalIssue><Title>Archives of pharmacal research</Title><ISOAbbreviation>Arch Pharm Res</ISOAbbreviation></Journal><ArticleTitle>Anti-inflammatory activity of flavonoids from Populus davidiana.</ArticleTitle><Pagination><MedlinePgn>1102-8</MedlinePgn></Pagination><Abstract><AbstractText>An in vitro bioassay-guide revealed that the methanol (MeOH) extract of the stem bark of Populus davidiana showed considerable inhibitory activity against cyclooxygenase (COX-1, COX-2). Continuous phytochemical study of the MeOH extract of this plant led to the isolation of ten flavonoids; sakuranetin (1), rhamnocitrin (2), 7-O-methylaromadendrin (3), naringenin (4), eriodictyol (5), aromadendrin (6), kaempferol (7), neosakuranin (8), sakuranin (9) and sakurenetin-5,4'-di-beta-D-glucopyranoside (10). Their structures were identified on the basis of their physicochemical and spectroscopic analyses. The isolated compounds, 1-10, were tested for their inhibitory activities against COX-1 and COX-2. Compound 7 was found to have potent inhibitory effect on COX-1 and a moderate effect on COX-2, meanwhile, compounds 1-6 showed moderate inhibition against COX-1 only. Moreover, compounds 5-8 exhibited suppressive effects on xanthine oxidase (XO). These results may explain, in part, the traditional uses of P. davidiana in ethnomedicine.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Zhang</LastName><ForeName>XinFeng</ForeName><Initials>X</Initials><AffiliationInfo><Affiliation>College of Pharmacy, Chungnam National University, Daejeon 305-764, Korea.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Hung</LastName><ForeName>Tran Manh</ForeName><Initials>TM</Initials></Author><Author ValidYN="Y"><LastName>Phuong</LastName><ForeName>Phuong Thien</ForeName><Initials>PT</Initials></Author><Author ValidYN="Y"><LastName>Ngoc</LastName><ForeName>Tran Minh</ForeName><Initials>TM</Initials></Author><Author ValidYN="Y"><LastName>Min</LastName><ForeName>Byung-Sun</ForeName><Initials>BS</Initials></Author><Author ValidYN="Y"><LastName>Song</LastName><ForeName>Kyung-Sik</ForeName><Initials>KS</Initials></Author><Author ValidYN="Y"><LastName>Seong</LastName><ForeName>Yeon Hee</ForeName><Initials>YH</Initials></Author><Author ValidYN="Y"><LastName>Bae</LastName><ForeName>KiHwan</ForeName><Initials>K</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType></PublicationTypeList></Article><MedlineJournalInfo><Country>Korea (South)</Country><MedlineTA>Arch Pharm Res</MedlineTA><NlmUniqueID>8000036</NlmUniqueID><ISSNLinking>0253-6269</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D000894">Anti-Inflammatory Agents, Non-Steroidal</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D052246">Cyclooxygenase 2 Inhibitors</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D016861">Cyclooxygenase Inhibitors</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D004791">Enzyme Inhibitors</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D005419">Flavonoids</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D010936">Plant Extracts</NameOfSubstance></Chemical><Chemical><RegistryNumber>11062-77-4</RegistryNumber><NameOfSubstance UI="D013481">Superoxides</NameOfSubstance></Chemical><Chemical><RegistryNumber>EC 1.14.99.1</RegistryNumber><NameOfSubstance UI="D051545">Cyclooxygenase 1</NameOfSubstance></Chemical><Chemical><RegistryNumber>EC 1.17.3.2</RegistryNumber><NameOfSubstance UI="D014969">Xanthine Oxidase</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D000894" MajorTopicYN="N">Anti-Inflammatory Agents, Non-Steroidal</DescriptorName><QualifierName UI="Q000302" MajorTopicYN="Y">isolation & purification</QualifierName><QualifierName UI="Q000494" MajorTopicYN="Y">pharmacology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D051545" MajorTopicYN="N">Cyclooxygenase 1</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D052246" MajorTopicYN="N">Cyclooxygenase 2 Inhibitors</DescriptorName><QualifierName UI="Q000302" MajorTopicYN="N">isolation & purification</QualifierName><QualifierName UI="Q000494" MajorTopicYN="N">pharmacology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D016861" MajorTopicYN="N">Cyclooxygenase Inhibitors</DescriptorName><QualifierName UI="Q000302" MajorTopicYN="N">isolation & purification</QualifierName><QualifierName UI="Q000494" MajorTopicYN="N">pharmacology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D004791" MajorTopicYN="N">Enzyme Inhibitors</DescriptorName><QualifierName UI="Q000494" MajorTopicYN="N">pharmacology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D005419" MajorTopicYN="N">Flavonoids</DescriptorName><QualifierName UI="Q000302" MajorTopicYN="Y">isolation & purification</QualifierName><QualifierName UI="Q000494" MajorTopicYN="Y">pharmacology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D006868" MajorTopicYN="N">Hydrolysis</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D009682" MajorTopicYN="N">Magnetic Resonance Spectroscopy</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D024301" MajorTopicYN="N">Plant Bark</DescriptorName><QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D010936" MajorTopicYN="N">Plant Extracts</DescriptorName><QualifierName UI="Q000032" MajorTopicYN="N">analysis</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D032107" MajorTopicYN="N">Populus</DescriptorName><QualifierName UI="Q000737" MajorTopicYN="Y">chemistry</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D013055" MajorTopicYN="N">Spectrophotometry, Infrared</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D013056" MajorTopicYN="N">Spectrophotometry, Ultraviolet</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D013481" MajorTopicYN="N">Superoxides</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D014969" MajorTopicYN="N">Xanthine Oxidase</DescriptorName><QualifierName UI="Q000037" MajorTopicYN="N">antagonists & inhibitors</QualifierName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>2007</Year><Month>1</Month><Day>18</Day><Hour>9</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2007</Year><Month>3</Month><Day>16</Day><Hour>9</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2007</Year><Month>1</Month><Day>18</Day><Hour>9</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">17225458</ArticleId><ArticleId IdType="doi">10.1007/BF02969299</ArticleId></ArticleIdList></PubmedData></pubmed></record>Pour manipuler ce document sous Unix (Dilib)
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