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- Publisher Website: 10.1016/j.jep.2012.08.012
- Scopus: eid_2-s2.0-84866737060
- PMID: 23034094
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Article: Bioassay-guided isolation of anti-inflammatory components from the root of Rehmannia glutinosa and its underlying mechanism via inhibition of iNOS pathway
Title | Bioassay-guided isolation of anti-inflammatory components from the root of Rehmannia glutinosa and its underlying mechanism via inhibition of iNOS pathway |
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Authors | |
Keywords | Anti-inflammation Bioassay-guided fractionation Cyclooxygenase-2 Inducible nitric oxide synthase Interleukin-6 Nitric oxide Prostaglandin E2 Rehmannia glutinosa Rehmapicrogenin |
Issue Date | 2012 |
Citation | Journal of Ethnopharmacology, 2012, v. 143, n. 3, p. 867-875 How to Cite? |
Abstract | Ethnopharmacological relevance: The root of Rehmannia glutinosa (RR) is commonly used to reduce inflammation in various traditional Chinese herbal formulae; however, little is known regarding its active component(s). Aim of study: The objective of the present study was to examine the active component(s) responsible for the anti-inflammatory activity of RR via anti-nitric oxide production assay-guided fractionation; and the underlying anti-inflammatory mechanism of action of such component(s) was further investigated. Materials and methods: Anti-nitric oxide (NO) activities with lipopolysaccharides (LPS)-stimulated RAW264.7 murine macrophages was used as screening platform. Gene, protein and inflammatory mediators' expression were also studied using real-time PCR, western blotting and ELISA, respectively. Results: Using anti-NO assay-guided fractionation, sub-fraction C3 (from 31.25 to 62.5 μg/ml, p=0.001 to 0.01) possessed 100-fold more potent anti-inflammatory effect than that of the aqueous extract of RR. Characterization of C3 showed that the anti-inflammatory effect could be partly due to the presence of rehmapicrogenin, which could significantly inhibit NO production (p<0.001). C3 was further demonstrated in blocking inflammation by inhibiting gene (p<0.001) and protein expression of inducible NO synthase (iNOS) dose-dependently. Besides, C3 also significantly inhibited the production of prostaglandin E2 (p<0.001 to 0.01), IL-6 (p<0.001 to 0.05) and COX-2 (p<0.05). Conclusions: Rehmapicrogenin was, for the first time, shown to possess nitric oxide inhibitory activities. Bioassay-guided fractionation demonstrated that rehmapicrogenin-containing subfraction C3 exhibited potent anti-inflammatory effect by inhibiting iNOS, COX-2 and IL-6, while rehmapicrogenin was only partially responsible for the anti-inflammatory effect of RR. © 2012 Elsevier Ireland Ltd. All rights reserved. |
Persistent Identifier | http://hdl.handle.net/10722/343105 |
ISSN | 2023 Impact Factor: 4.8 2023 SCImago Journal Rankings: 0.936 |
DC Field | Value | Language |
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dc.contributor.author | Liu, Cheuk Lun | - |
dc.contributor.author | Cheng, Ling | - |
dc.contributor.author | Ko, Chun Hay | - |
dc.contributor.author | Wong, Chun Wai | - |
dc.contributor.author | Cheng, Wai Hing | - |
dc.contributor.author | Cheung, David Wing Shing | - |
dc.contributor.author | Leung, Ping Chung | - |
dc.contributor.author | Fung, Kwok Pui | - |
dc.contributor.author | Bik-San Lau, Clara | - |
dc.date.accessioned | 2024-05-10T09:05:28Z | - |
dc.date.available | 2024-05-10T09:05:28Z | - |
dc.date.issued | 2012 | - |
dc.identifier.citation | Journal of Ethnopharmacology, 2012, v. 143, n. 3, p. 867-875 | - |
dc.identifier.issn | 0378-8741 | - |
dc.identifier.uri | http://hdl.handle.net/10722/343105 | - |
dc.description.abstract | Ethnopharmacological relevance: The root of Rehmannia glutinosa (RR) is commonly used to reduce inflammation in various traditional Chinese herbal formulae; however, little is known regarding its active component(s). Aim of study: The objective of the present study was to examine the active component(s) responsible for the anti-inflammatory activity of RR via anti-nitric oxide production assay-guided fractionation; and the underlying anti-inflammatory mechanism of action of such component(s) was further investigated. Materials and methods: Anti-nitric oxide (NO) activities with lipopolysaccharides (LPS)-stimulated RAW264.7 murine macrophages was used as screening platform. Gene, protein and inflammatory mediators' expression were also studied using real-time PCR, western blotting and ELISA, respectively. Results: Using anti-NO assay-guided fractionation, sub-fraction C3 (from 31.25 to 62.5 μg/ml, p=0.001 to 0.01) possessed 100-fold more potent anti-inflammatory effect than that of the aqueous extract of RR. Characterization of C3 showed that the anti-inflammatory effect could be partly due to the presence of rehmapicrogenin, which could significantly inhibit NO production (p<0.001). C3 was further demonstrated in blocking inflammation by inhibiting gene (p<0.001) and protein expression of inducible NO synthase (iNOS) dose-dependently. Besides, C3 also significantly inhibited the production of prostaglandin E2 (p<0.001 to 0.01), IL-6 (p<0.001 to 0.05) and COX-2 (p<0.05). Conclusions: Rehmapicrogenin was, for the first time, shown to possess nitric oxide inhibitory activities. Bioassay-guided fractionation demonstrated that rehmapicrogenin-containing subfraction C3 exhibited potent anti-inflammatory effect by inhibiting iNOS, COX-2 and IL-6, while rehmapicrogenin was only partially responsible for the anti-inflammatory effect of RR. © 2012 Elsevier Ireland Ltd. All rights reserved. | - |
dc.language | eng | - |
dc.relation.ispartof | Journal of Ethnopharmacology | - |
dc.subject | Anti-inflammation | - |
dc.subject | Bioassay-guided fractionation | - |
dc.subject | Cyclooxygenase-2 | - |
dc.subject | Inducible nitric oxide synthase | - |
dc.subject | Interleukin-6 | - |
dc.subject | Nitric oxide | - |
dc.subject | Prostaglandin E2 | - |
dc.subject | Rehmannia glutinosa | - |
dc.subject | Rehmapicrogenin | - |
dc.title | Bioassay-guided isolation of anti-inflammatory components from the root of Rehmannia glutinosa and its underlying mechanism via inhibition of iNOS pathway | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1016/j.jep.2012.08.012 | - |
dc.identifier.pmid | 23034094 | - |
dc.identifier.scopus | eid_2-s2.0-84866737060 | - |
dc.identifier.volume | 143 | - |
dc.identifier.issue | 3 | - |
dc.identifier.spage | 867 | - |
dc.identifier.epage | 875 | - |
dc.identifier.eissn | 1872-7573 | - |