Secondary metabolites from Gentiana cruciata L. and their anti-inflammatory and analgesic activities

dc.contributor.authorKonya, Rima
dc.contributor.authorReis, Rengin
dc.contributor.authorSipahi, Hande
dc.contributor.authorBarta, Anita
dc.contributor.authorHohmann, Judit
dc.contributor.authorKirmizibekmez, Hasan
dc.date.accessioned2023-02-21T12:37:00Z
dc.date.available2023-02-21T12:37:00Z
dc.date.issued2022-01-01
dc.description.abstractA previously unreported secoiridoid glycoside, cruciatoside (1) was isolated from the aerial parts of Gentiana cruciata L. along with ten known compounds eustomoside (2), eustomorusside (3), gentiopicroside (4), 6'-O-beta-D-glucopyranosyl gentiopicroside (5), loganic acid (6), isoorientin (7), isovitexin (8), isovitexin 2''-(E)-ferulate (9), mangiferin (10), and 2-methyl-inositol (11). The chemical structures of the isolates were elucidated based on extensive 1 D and 2 D NMR experiments as well as HRMS analysis. All isolates were evaluated for their in vitro anti-inflammatory and analgesic activities. Compounds 9, 4, and 7 (200 mu M) showed moderate anti-inflammatory activity by inhibiting nitrite production from LPS-induced RAW 264.7 macrophage cells, with the inhibition rates of 39.5\%, 25.8\% and 22.9\% respectively without exhibiting substantial cytotoxicity. Besides, 1, 2, 4, and 7 exerted the highest decrease in IL-6 levels. Moreover, compound 4 showed in vitro analgesic activity by decreasing the PGE(2) level comparable to the reference drugs.
dc.identifier.doi10.1080/14786419.2022.2144301
dc.identifier.urihttps://hdl.handle.net/11443/2184
dc.identifier.urihttp://dx.doi.org/10.1080/14786419.2022.2144301
dc.identifier.wosWOS:000880271300001
dc.publisherTAYLOR \& FRANCIS LTD
dc.relation.ispartofNATURAL PRODUCT RESEARCH
dc.subjectGentiana cruciata
dc.subjectGentianaceae
dc.subjectsecoiridoid
dc.subjectcruciatoside
dc.subjectanti-inflammatory and analgesic activity
dc.titleSecondary metabolites from Gentiana cruciata L. and their anti-inflammatory and analgesic activities
dc.typeArticle

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