Engelheptanoxides behave as liver X receptor α agonists

被引:0
|
作者
Liang, Yu-Hsuan [1 ]
Luo, Yu-Han [2 ]
Chen, Ih-Sheng [3 ]
Lin, Hsiang-Ru [4 ]
机构
[1] Natl Yang Ming Chiao Tung Univ, Inst Clin Med, Taipei 112304, Taiwan
[2] Natl Yang Ming Chiao Tung Univ, Inst Tradit Med, Taipei 112304, Taiwan
[3] Kaohsiung Med Univ, Coll Pharm, Sch Pharm, 100 Shih Chuan 1st Rd, Kaohsiung 80708, Taiwan
[4] Natl Kaohsiung Normal Univ, Coll Sci, Dept Chem, 62 Shenjhong Rd, Kaohsiung 82446, Taiwan
关键词
Engelhardia roxburghiana; Engelheptanoxide; liver X receptor (LXR); ENGELHARDIA-ROXBURGHIANA; LXR-ALPHA; ACTIVATION; CHOLESTEROL; EXPRESSION; TRANSCRIPTION; ASTILBIN;
D O I
10.1007/s00044-023-03016-y
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Engelheptanoxide A and C are the active ingredients isolated from Engelhardia roxburghiana, a novel traditional herbal medicine exerting pharmacological effects including the antitubercular effect. Liver X receptor (LXR) acts as a ligand-activated transcription factor that can exert multi-pharmacological functions. In this study, the activity of engelheptanoxide A and C against LXR alpha was evaluated by the transient transfection reporter and mammalian one-hybrid assays. The results showed that engelheptanoxide A and C respectively transactivated CYP7A1, ABCA1, and Gal4 promoters in the dose-dependent manner. Furthermore, the docking study demonstrated that engelheptanoxide A and C can contact with the LXR alpha ligand binding pocket in the similar manner as 22(R)-hydroxycholesterol, an endogenous LXR alpha agonist, to agonize LXR alpha. These results indicated that Engelhardia roxburghiana might be able to exert pharmacological effects through LXR alpha pathway.
引用
收藏
页码:434 / 441
页数:8
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