Lignans from Potentilla kleiniana and their cytotoxicity

Abstract

Potentilla kleiniana belongs to the family Rosaceae, which distributes in Central Asia, East Asia and Southeast Asia. In China, this plant is mainly found in east, south and southwest provinces. P. kleiniana has been prescribed for the treatment of various diseases in the field of traditional Chinese medicine, such as cough, fever, tuberculosis, mastitis, rheumatoid arthritis. Our previous study found that P. kleiniana had a certain cytotoxicity on tumor cells. The purpose of this paper was to investigate the chemical constituents of P. kleiniana and their cytotoxicity on tumor cells. The 60% ethanol extract of P. kleiniana were isolated by D-101 macroporous adsorptive resins, silica gel, Sephadex LH-20, Toyopearl HW-40F, semi-preparative high performance liquid chromatography and other methods, and their chemical structures were elucidated on the basis of physicochemical properties, NMR and HR-ESI-MS analysis. Meanwhile, all these compounds were evaluated for cytotoxicity against human cervical cancer cell line Hela. The results were as follows: (1) Thirteen lignans were isolated and identified as (+)-pionresinol (1), (+)-8-hydroxypinoresinol (2), (+)-syringaresinol (3), (+)-medioresinol (4), (+)-pionresinol-4-O-β-D-glucopyranoside (5), (+)-8′-hydroxypinoresinol-4-O-β-D-glucopyranoside (6), (+)-8′-hydroxypinoresinol-4′-O-β-D-glucopyranoside (7), (+)-pinoresinol-8′-O-β-D-glucopyranoside (8), schilignan F (9), (+)-pionresinol-4, 4′-O-bisglucopyranoside (10), (+)-lariciresinol-4′-O-β-D-glucopyranoside (11), neoolivil-4-O-β-D-glucopyranoside (12), 3,3′-bis［3,4-dihydro-4-hydroxy-6-methoxy-2H-1-benzopyran］(13). Among them, compounds 1-4, 7, 8, 10, 12, 13 were isolated from genus Potentilla for the first time, and compounds 5, 6, 9, 11 were isolated from P. kleiniana for the first time. (2) Cytotoxicity studies showed that compounds 1, 3 and 4 display certain inhibitory activities against Hela cells with IC50 values of (69.94 ± 1.89), (66.25 ± 2.11), (59.81 ± 1.73) μmol·L-1, respectively. Therefore, the study enriches the chemical constituents of P. kleiniana, and provides a material basis for the development of anti-cervical cancer drugs.

Keywords

• potentilla kleiniana
• chemical constituents
• isolation and purification
• structural identification
• lignans
• cytotoxicity
• antitumor activity