Soluble Epoxide Hydrolase Inhibitory and Anti-inflammatory Components from the Leaves ofEucommia ulmoidesOliver (Duzhong)

杜仲 化学 环氧化物水解酶2 立体化学 抑制性突触后电位 山奈酚 槲皮素 IC50型 生物化学 传统医学 体外 生物 医学 病理 神经科学 中医药 替代医学 抗氧化剂
作者
Meng-Meng Bai,Wei Shi,Jun‐Mian Tian,Ming Lei,Jang Hoon Kim,Ya Nan Sun,Young Ho Kim,Jin‐Ming Gao
出处
期刊:Journal of Agricultural and Food Chemistry [American Chemical Society]
卷期号:63 (8): 2198-2205 被引量:79
标识
DOI:10.1021/acs.jafc.5b00055
摘要

Eucommia 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.
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