Bioassay-Guided Fractionation and Biological Activity of Cardenolides from Streptocaulon juventas

被引:1
|
作者
Xu, Yunhui [2 ]
Xu, Jian [1 ]
Zhu, Wanfang [3 ]
Yan, Yanling [4 ,5 ,6 ]
Jiang, Xueyang [7 ]
Xie, Zijian [2 ]
Feng, Feng [1 ,8 ]
Zhang, Jie [1 ]
机构
[1] China Pharmaceut Univ, Dept Nat Med Chem, Nanjing 210038, Peoples R China
[2] Marshall Univ, Joan C Edwards Sch Med, Dept Biomed Sci, Huntington, WV USA
[3] Changchun Univ Chinese Med, Coll Pharm, Changchun, Peoples R China
[4] Marshall Univ, Joan C Edwards Sch Med, Dept Clin & Translat Sci, Huntington, WV USA
[5] Marshall Univ, Joan C Edwards Sch ofMedicine, Dept Biomed Sci, UnitedStates, Huntington, WV USA
[6] Marshall Univ, Joan C Edwards Sch Med, Dept Med, Huntington, WV USA
[7] Anhui Univ Chinese Med, Dept Med Chem, Hefei, Peoples R China
[8] China Pharmaceut Univ, Dept Nat Med Chem, 639 Long Mian Da Dao, Nanjing 211198, Peoples R China
基金
美国国家卫生研究院;
关键词
Streptocaulon juventas; Asclepiadaceace; cardiotonic steroids; Na/K-ATPase; NA+/K+-ATPASE; OUABAIN INTERACTION; BINDING; CONSTITUENTS; ACTIVATION; RECEPTOR; BIOTRANSFORMATION; DIGITOXIGENIN; GLYCOSIDES; PATHWAYS;
D O I
10.1055/a-2114-5371
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The discovery that Na/K-ATPase acts as a signal transducer led us to investigate the structural diversity of cardiotonic steroids and study their ligand effects. By applying Na/K-ATPase activity assay-guided fractionation, we isolated a total of 20 cardiotonic steroids from Streptocaulon juventas , including an undescribed juventasoside B ( 10 ) and 19 known cardiotonic steroids. Their structures have been elucidated. Using our platform of purified Na/K-ATPase and an LLC-PK1 cell model, we found that 10 , at a concentration that induces less than 10% Na/K-ATPase inhibition, can stimulate the Na/K-ATPase/Src receptor complex and selectively activate downstream pathways, ultimately altering prostate cancer cell growth. By assessing the ligand effect of the isolated cardiotonic steroids, we found that the regulation of cell viability by the isolated cardiotonic steroids was not associated with their inhibitory potencies against Na/K-ATPase activity but reflected their ligand-binding affinity to the Na/K-ATPase receptor. Based on this discovery, we identified a unique active cardiotonic steroid, digitoxigenin ( 1 ), and verified that it can protect LLC-PK1 cells from hypoxic injury, implicating its potential use in ischemia/reperfusion injury and inducing collagen synthesis in primary human dermal fibroblast cells, and implicating that compound 2 is the molecular basis of the wound healing activity of S. juventas .
引用
收藏
页码:1444 / 1456
页数:13
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