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Bioactivity-guided isolation of polyacetylenes with inhibitory activity against NO production in LPS-activated RAW264.7 macrophages from the rhizomes of Atractylodes macrocephala
Authors:Chun-Mei Yao  Xiu-Wei Yang
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
Abstract:

Ethnopharmacological relevance

The 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 methods

Inhibitory 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.

Results

Seven new polyacetylenes, named atractylodemaynes A–G (17), along with eight known ones (815) 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.

Conclusion

The results demonstrated that the polyacetylenes might greatly contribute to the anti-inflammatory activity of the rhizomes of A. macrocephala.
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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