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Download fileSoluble Epoxide Hydrolase Inhibitory and Anti-inflammatory Components from the Leaves of Eucommia ulmoides Oliver (Duzhong)
journal contribution
posted on 04.03.2015, 00:00 authored by Meng-Meng Bai, Wei Shi, Jun-Mian Tian, Ming Lei, Jang Hoon Kim, Ya Nan Sun, Young Ho Kim, Jin-Ming GaoEucommia ulmoides leaves have been
used as a functional food and drink in China. The purpose of this
study was to identify the bioactive constituents with soluble epoxide
hydrolase (sEH) inhibitory activity and anti-inflammatory properties.
Twenty-seven known compounds (1–27) were isolated from the leaves of E. ulmoides Oliver, and their structures were identified by NMR and ESIMS analysis;
three of these, 2,5-dimethoxy-3-glucopyranosyl cinnamic alcohol (11), foliasalacioside E2 (26), and
icariside F2 (27), were obtained from this
plant for the first time. Compounds 1–7 exhibited soluble epoxide hydrolase (sEH) inhibitory activity at
100 μM; among them, quercetin (1) and kaempferol
(5) displayed potential activities with IC50 values of 22.5 ± 0.9 and 31.3 ± 2.6 μM, respectively,
with noncompetitive inhibition mode. Nuclear factor kappa B (NF-κB)
inhibitory activity of the isolated compounds was evaluated by the
NF-κB liciferase assay in HepG2 cells. Compounds 1, 9, 20, and 27 displayed
potent NF-κB inhibitory effects, with IC50 values
of 15.14 ± 2.29, 15.23 ± 2.34, 16.88 ± 2.17, and 16.25
± 2.19 μM, respectively, whereas other compounds showed
weak inhibition of NF-κB transcriptional activity ranging from
17.54 to 92.6 μM. A structure–activity relationship of
flavonoids 1–9 was also discussed.
The results obtained in this work might contribute to the understanding
of pharmacological activities of E. ulmoides leaves and further investigation on its potential application values
for food and drug.