Suppr超能文献

刺五加蒸叶的成分及其对HepG2细胞中PPAR活性的影响。

Components from the steamed leaves of Acanthopanax koreanum and their effects on PPAR activity in HepG2 cells.

作者信息

Kim Jeong Ah, Song Seek Bean, Yang Seo Young, Kim Young Ho

机构信息

College of Pharmacy, Chungnam National University, Daejeon 305-764, Korea.

出版信息

Nat Prod Commun. 2011 Sep;6(9):1233-6.

Abstract

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.

摘要

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。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验