Anti-inflammatory activities of the triterpene acids from the resin of Boswellia carteri

Boswellic acids are the main well-known active components of the resin of Boswellia carteri (Burseraceae) and these are still dealing with the ethnomedicinal use for the treatment of rheumatoid arthritis and other inflammatory diseases. Although several studies have already been reported on the phar...

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Published inJournal of ethnopharmacology Vol. 107; no. 2; pp. 249 - 253
Main Authors Banno, Norihiro, Akihisa, Toshihiro, Yasukawa, Ken, Tokuda, Harukuni, Tabata, Keiichi, Nakamura, Yuji, Nishimura, Reiko, Kimura, Yumiko, Suzuki, Takashi
Format Journal Article
LanguageEnglish
Published Shannon Elsevier Ireland Ltd 19.09.2006
Elsevier
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Summary:Boswellic acids are the main well-known active components of the resin of Boswellia carteri (Burseraceae) and these are still dealing with the ethnomedicinal use for the treatment of rheumatoid arthritis and other inflammatory diseases. Although several studies have already been reported on the pharmacological properties, especially on the anti-inflammatory activity, of Boswellia carteri resin and boswellic acids, the ethnomedicinal importance of Boswellia carteri and its components, boswellic acids, prompted us to undertake detailed investigation on the constituents of the resin and their anti-inflammatory activity. Fifteen triterpene acids, viz., seven of the β-boswellic acids (ursane-type) ( 1– 7), two of the α-boswellic acids (oleanane-type) ( 8, 9), two of the lupeolic acids (lupane-type) ( 10, 11), and four of the tirucallane-type ( 12– 14, 16), along with two cembrane-type diterpenes ( 17, 18), were isolated and identified from the methanol extract of the resin of Boswellia carteri. Upon evaluation of 17 compounds, 1– 14 and 16– 18, and compound 15, semi-synthesized from 14 by acetylation, for their inhibitory activity against 12- O-tetradecanoylphorbol-13-acetate (TPA)-induced inflammation (1 μg/ear) in mice, all of the compounds, except for 18, exhibited marked anti-inflammatory activity with a 50% inhibitory dose (ID 50) of 0.05–0.49 mg/ear.
Bibliography:http://dx.doi.org/10.1016/j.jep.2006.03.006
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0378-8741
1872-7573
DOI:10.1016/j.jep.2006.03.006