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- Publisher Website: 10.1021/jm9006164
- Scopus: eid_2-s2.0-71049149246
- PMID: 19835377
- WOS: WOS:000271427900023
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Article: Identification of the bioactive constituent and its mechanisms of action in mediating the anti-inflammatory effects of black cohosh and related Cimicifuga species on human primary blood macrophages
Title | Identification of the bioactive constituent and its mechanisms of action in mediating the anti-inflammatory effects of black cohosh and related Cimicifuga species on human primary blood macrophages | ||||||
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Authors | |||||||
Issue Date | 2009 | ||||||
Publisher | American Chemical Society. The Journal's web site is located at http://pubs.acs.org/jmc | ||||||
Citation | Journal Of Medicinal Chemistry, 2009, v. 52 n. 21, p. 6707-6715 How to Cite? | ||||||
Abstract | Cimicifuga species have been used as traditional medicinal herbs to treat inflammation and symptoms associated with menopause in Asia, Europe, and North America. However, the underlying mechanism of their anti-inflammatory effects remains to be investigated. With bioactivity guided purification involving the use of partitioning extraction and high performance liquid chromatography, we isolated one of the key bioactive constituents from the rhizome extracts of Cimicifuga racemosa. By NMR spectroscopy, the molecule was identified to be cimiracemate A (1). This compound (140 μM) suppressed the lipopolysaccharide-induced TNF-R production in the blood macrophages by 47 (19% and 58 (30% at LPS concentrations of 1 ng/mL and 10 ng/mL, respectively. The antiinflammatory activity of compound 1 may be due to its modulation of a signaling mitogen activated protein kinase and transcription factor nuclear factor-kappaB activities. Compound 1 was found in other Cimicifuga species. Our data indicate that compound 1 or its chemical analogues may have the potential to be further developed as a new class of therapeutic agent. © 2009 American Chemical Society. | ||||||
Persistent Identifier | http://hdl.handle.net/10722/127585 | ||||||
ISSN | 2023 Impact Factor: 6.8 2023 SCImago Journal Rankings: 1.986 | ||||||
ISI Accession Number ID |
Funding Information: This project was supported in part by grants from Prof Francis SK Lau and Mr. William Au Research Fund as well as Purapharm International awarded to Dr. A. Lau. We thank Genome Research Centre of The University of Hong Kong for facility support. We also thank Prof. PY Qian from The University of Science and Technology for providing UPLC-TOF-ESI-MS facilities for spectroscopic analysis and Miss S. Dash for her time and assistance in this regard. Both SCCC and JCBL contributed equally to this manuscript. | ||||||
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Yang, CLH | en_HK |
dc.contributor.author | Chik, SCC | en_HK |
dc.contributor.author | Li, JCB | en_HK |
dc.contributor.author | Cheung, BKW | en_HK |
dc.contributor.author | Lau, ASY | en_HK |
dc.date.accessioned | 2010-10-31T13:34:06Z | - |
dc.date.available | 2010-10-31T13:34:06Z | - |
dc.date.issued | 2009 | en_HK |
dc.identifier.citation | Journal Of Medicinal Chemistry, 2009, v. 52 n. 21, p. 6707-6715 | en_HK |
dc.identifier.issn | 0022-2623 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/127585 | - |
dc.description.abstract | Cimicifuga species have been used as traditional medicinal herbs to treat inflammation and symptoms associated with menopause in Asia, Europe, and North America. However, the underlying mechanism of their anti-inflammatory effects remains to be investigated. With bioactivity guided purification involving the use of partitioning extraction and high performance liquid chromatography, we isolated one of the key bioactive constituents from the rhizome extracts of Cimicifuga racemosa. By NMR spectroscopy, the molecule was identified to be cimiracemate A (1). This compound (140 μM) suppressed the lipopolysaccharide-induced TNF-R production in the blood macrophages by 47 (19% and 58 (30% at LPS concentrations of 1 ng/mL and 10 ng/mL, respectively. The antiinflammatory activity of compound 1 may be due to its modulation of a signaling mitogen activated protein kinase and transcription factor nuclear factor-kappaB activities. Compound 1 was found in other Cimicifuga species. Our data indicate that compound 1 or its chemical analogues may have the potential to be further developed as a new class of therapeutic agent. © 2009 American Chemical Society. | en_HK |
dc.language | eng | en_HK |
dc.publisher | American Chemical Society. The Journal's web site is located at http://pubs.acs.org/jmc | en_HK |
dc.relation.ispartof | Journal of Medicinal Chemistry | en_HK |
dc.title | Identification of the bioactive constituent and its mechanisms of action in mediating the anti-inflammatory effects of black cohosh and related Cimicifuga species on human primary blood macrophages | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Li, JCB: jamesli@hku.hk | en_HK |
dc.identifier.email | Lau, ASY: asylau@hku.hk | en_HK |
dc.identifier.authority | Li, JCB=rp00496 | en_HK |
dc.identifier.authority | Lau, ASY=rp00474 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1021/jm9006164 | en_HK |
dc.identifier.pmid | 19835377 | - |
dc.identifier.scopus | eid_2-s2.0-71049149246 | en_HK |
dc.identifier.hkuros | 171678 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-71049149246&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 52 | en_HK |
dc.identifier.issue | 21 | en_HK |
dc.identifier.spage | 6707 | en_HK |
dc.identifier.epage | 6715 | en_HK |
dc.identifier.eissn | 1520-4804 | - |
dc.identifier.isi | WOS:000271427900023 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.scopusauthorid | Yang, CLH=26668171500 | en_HK |
dc.identifier.scopusauthorid | Chik, SCC=6507803546 | en_HK |
dc.identifier.scopusauthorid | Li, JCB=23103447500 | en_HK |
dc.identifier.scopusauthorid | Cheung, BKW=9634391200 | en_HK |
dc.identifier.scopusauthorid | Lau, ASY=7202626202 | en_HK |
dc.identifier.issnl | 0022-2623 | - |