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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<term>Cyclooxygenase 2 Inhibitors (isolation & purification)</term>
<term>Cyclooxygenase 2 Inhibitors (pharmacology)</term>
<term>Cyclooxygenase Inhibitors (isolation & purification)</term>
<term>Cyclooxygenase Inhibitors (pharmacology)</term>
<term>Enzyme Inhibitors (pharmacology)</term>
<term>Flavonoids (isolation & purification)</term>
<term>Flavonoids (pharmacology)</term>
<term>Hydrolysis (MeSH)</term>
<term>Magnetic Resonance Spectroscopy (MeSH)</term>
<term>Plant Bark (chemistry)</term>
<term>Plant Extracts (analysis)</term>
<term>Populus (chemistry)</term>
<term>Spectrophotometry, Infrared (MeSH)</term>
<term>Spectrophotometry, Ultraviolet (MeSH)</term>
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<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>
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<term>Cyclooxygenase 2 Inhibitors</term>
<term>Cyclooxygenase Inhibitors</term>
<term>Flavonoids</term>
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<term>Cyclooxygenase 2 Inhibitors</term>
<term>Cyclooxygenase Inhibitors</term>
<term>Enzyme Inhibitors</term>
<term>Flavonoids</term>
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<term>Inhibiteurs des cyclooxygénases</term>
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<term>Superoxydes</term>
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<term>Flavonoïdes</term>
<term>Inhibiteurs de la cyclooxygénase 2</term>
<term>Inhibiteurs des cyclooxygénases</term>
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<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>
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<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>
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<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>
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