Fu Hai-Jian, Zhao Yang, Zhou Yu-Ren, Bao Bei-Hua, Du Yun, Li Jian-Xin
State Key Lab of Analytical Chemistry for Life Science and Collaborative Innovation Center of Chemistry for Life Sciences, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing, Jiangsu 210093, PR China.
State Key Lab of Analytical Chemistry for Life Science and Collaborative Innovation Center of Chemistry for Life Sciences, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing, Jiangsu 210093, PR China.
Eur J Pharm Sci. 2015 Aug 30;76:33-47. doi: 10.1016/j.ejps.2015.04.021. Epub 2015 Apr 28.
Tryptophan hydroxylase 1 (Tph-1) initiates the biosynthesis of peripheral serotonin. As peripheral serotonin suppresses bone formation, inhibitor of Tph-1 provides a useful tool to discover anabolic agents for osteoporosis. In the present study, series of ursolic acid (UA) derivatives were synthesized, and their inhibitory activity on serotonin biosynthesis and cytotoxicity were evaluated. Among the derivatives, 8d with potent inhibitory activity on serotonin was applied for further research. The data revealed that 8d significantly inhibited protein and mRNA expressions of Tph-1, and an SPR study indicated that 8d directly interacted to Tph-1 with a binding affinity of KD=15.09μM. Oral administration of 8d significantly prevented bone loss via suppressing serotonin biosynthesis without estrogenic side-effects in ovariectomized (OVX) rats.
色氨酸羟化酶1(Tph-1)启动外周5-羟色胺的生物合成。由于外周5-羟色胺会抑制骨形成,Tph-1抑制剂为发现骨质疏松症的合成代谢药物提供了一种有用的工具。在本研究中,合成了一系列熊果酸(UA)衍生物,并评估了它们对5-羟色胺生物合成的抑制活性和细胞毒性。在这些衍生物中,对5-羟色胺具有强抑制活性的8d被用于进一步研究。数据显示,8d显著抑制Tph-1的蛋白质和mRNA表达,一项表面等离子体共振(SPR)研究表明,8d与Tph-1直接相互作用,结合亲和力KD=15.09μM。在去卵巢(OVX)大鼠中,口服8d通过抑制5-羟色胺生物合成显著预防了骨质流失,且无雌激素副作用。