Bioactivity-guided isolation of polyacetylenes with inhibitory activity against NO production in LPS-activated RAW264.7 macrophages from the rhizomes of Atractylodes macrocephala |
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Authors: | Chun-Mei Yao Xiu-Wei Yang |
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Affiliation: | State Key Laboratory of Natural and Biomimetic Drugs (Peking University), Department of Natural Medicines, School of Pharmaceutical Sciences, Peking University Health Science Center, Peking University, Beijing 100191, China |
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Abstract: | Ethnopharmacological relevanceThe rhizome of Atractylodes macrocephala (Compositae) is one of the most well-known traditional Chinese medicine in China, Japan and Korea, which has a long history of use for the treatment of splenic asthenia, edema, anorexia, and excessive perspiration, etc. As active compounds of anti-inflammatory activity of this medicinal plant have not been fully elucidated, the aim of this study was to isolate and identify the active constituents inhibiting nitric oxide (NO) production from the rhizomes of A. macrocephala.Materials and methodsInhibitory activity against NO production in lipopolysaccharide-activated RAW264.7 macrophages was evaluated by Griess reaction. Fifteen polyacetylenes were isolated from the active ethyl acetate extract using activity-guided screening. The structures of all compounds were elucidated by spectroscopic methods and comparison with published data. The compounds were further tested for their inhibitory activity against NO production.ResultsSeven new polyacetylenes, named atractylodemaynes A–G (1–7), along with eight known ones (8–15) were isolated. Compound 14 was isolated for the first time from the rhizomes of A. macrocephala. The study showed that the tested compounds exhibited inhibitory activity against NO production in a dose-dependent manner. Among them, compounds 10, 11 and 12 had relatively stronger inhibitory effect with IC50 values of 28, 23 and 19 μM, respectively.ConclusionThe results demonstrated that the polyacetylenes might greatly contribute to the anti-inflammatory activity of the rhizomes of A. macrocephala. |
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Keywords: | AMR, Atractylodis Macrocephalae Rhizoma AO-I, atractylenolide I AO-III, atractylenolide III NO, nitric oxide LPS, lipopolysaccharides MTT, 3-(4,5-Dimethyl-2-thiazolyl)-2,5-diphenyl-2H-tetrazolium bromide IND, indomethacin L-NIL, L-N6-(1-iminoethyl)-lysine CC, column chromatography HPLC, high-performance liquid chromatography HRESIMS, high-resolution electric spray ion mass spectrum NMR, nuclear magnetic resonance 1H&ndash 1H COSY, 1H&ndash 1H correlated spectroscopy HSQC, heteronuclear single quantum correlation HMBC, heteronuclear multiple bond correlation EtOH, ethanol CHX, cyclohexane EtOAc, ethyl acetate BuOH, n-butanol |
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