Kim Jeong Ah, Song Seek Bean, Yang Seo Young, Kim Young Ho
College of Pharmacy, Chungnam National University, Daejeon 305-764, Korea.
Nat Prod Commun. 2011 Sep;6(9):1233-6.
Three ent-kaurane diterpenes (1-3), four lupane-triterpene glycosides (4-7), and an oleanane-triterpene glycoside (8) were isolated from the ethyl acetate and water extracts of the steamed leaves of Acanthopanax koreanum using a combination of various column chromatographies. The structures of the isolates were determined by 1H-, 13C-NMR spectroscopy and mass spectrometry. To investigate the biological effects of the eight compounds (1-8) on peroxisome proliferator-activated receptor gamma (PPARgamma), luciferase reporter assays were used. Among the tested compounds, ent-kaur-16-en-19-oic acid (1), 16alpha-hydroxy-ent-kauran-19-oic acid (2), and 17-hydroxy-ent-kaur-15-en-19-oic acid (3) showed considerable effects on PPARgamma activity, compared with the positive control, troglitazone. To evaluate specificity and sensitivity of the active compounds (1-3) in the regulation of transactivation of PPARs, Gal4-PPARs-LBD luciferase reporter assays were examined. In this study, the three ent-kaurane diterpenes (1-3) were found to up-regulate PPARbeta/delta and PPARgamma activities, whereas they did not activate PPARalpha activity.
采用多种柱色谱法相结合的方法,从辽东楤木蒸叶的乙酸乙酯提取物和水提取物中分离出3种对映-贝壳杉烷二萜(1-3)、4种羽扇豆烷三萜糖苷(4-7)和1种齐墩果烷三萜糖苷(8)。通过¹H-、¹³C-NMR光谱和质谱确定了分离物的结构。为了研究这8种化合物(1-8)对过氧化物酶体增殖物激活受体γ(PPARγ)的生物学作用,采用了荧光素酶报告基因检测法。在测试的化合物中,与阳性对照曲格列酮相比,对映-贝壳杉-16-烯-19-酸(1)、16α-羟基对映-贝壳杉烷-19-酸(2)和17-羟基对映-贝壳杉-15-烯-19-酸(3)对PPARγ活性有显著影响。为了评估活性化合物(1-3)在PPARs反式激活调节中的特异性和敏感性,检测了Gal4-PPARs-LBD荧光素酶报告基因检测法。在本研究中,发现这3种对映-贝壳杉烷二萜(1-3)上调PPARβ/δ和PPARγ活性,而不激活PPARα活性。