Activity-guided separation of antioxidant response element (ARE)-inducing constituents from the rhizomes of Atractylodis Rhizoma Alba was performed by the combination of centrifugal partition chromatography (CPC) and an ARE luciferase reporter assay. From 3 g of the active -hexane fraction, one polyacetylene, (6,12)-tetradeca-6,12-dien-8,10-diyne-1,3-diyl diacetate (47.3 mg), and two sesquiterpenes, atractylenolide I (40.9 mg), and selina-4(14),7(11)-dien-8-one (6.0 mg) were successfully isolated by CPC with -hexane⁻ethyl acetate⁻methanol⁻water (8:2:8:2, /). The chemical structures of the isolated compounds were determined by ¹H- and C-NMR and ESI-MS. Among the isolated compounds, (6,12)-tetradeca-6,12-diene-8,10-diyne-1,3-diol diacetate and selina-4(14),7(11)-dien-8-one increased ARE activity 32.9-fold and 16.6-fold, respectively, without significant cytotoxicity, when 5 µM sulforaphane enhanced ARE activity 27.1-fold. However, atractylenolide I did not increase ARE activity at 100 µM, and showed cytotoxicity at concentrations over 10 µM.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6225303PMC
http://dx.doi.org/10.3390/molecules23092274DOI Listing

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