Natural constituents from Cortex Mori Radicis as new pancreatic lipase inhibitors

脂肪酶 化学 IC50型 酶 水解 生物化学 胰脂肪酶 抑制性突触后电位 体外 传统医学 立体化学 医学 内科学
作者
Xu-Dong Hou,Guang‐Bo Ge,Zi-Miao Weng,Ziru Dai,Yue-Hong Leng,Lele Ding,Lingling Jin,Yang Yu,Yun‐Feng Cao,Jie Hou
出处
期刊:Bioorganic Chemistry [Elsevier BV]
卷期号:80: 577-584 被引量:57
标识
DOI:10.1016/j.bioorg.2018.07.011
摘要

Pancreatic lipase (PL), a key enzyme responsible for the hydrolysis of triacylglycerides in the gastrointestinal tract, has been identified as the therapeutic target for the regulation of lipid absorption. In the present study, six major constituents from a famous Chinese herbal medicine Cortex Mori Radicis (also named sangbaipi in Chinese), have been collected and their inhibitory effects on PL have been carefully investigated and well characterized by a fluorescence-based assay. The results clearly demonstrated that all tested bioactive constituents from Cortex Mori Radicis including sanggenone C (SC), sanggenone D (SD), kuwanon C (KC), kuwanon G (KG), morin and morusin displayed strong to moderate inhibitory effects towards PL with the IC50 values ranging from 0.77 μM to 20.56 μM. Further investigations on inhibition kinetics demonstrated that SC, SD, KC and KG functioned as potent and mixed inhibitors against PL-mediated 4-MU oleate hydrolysis, with the Ki values less than 5.0 μM. Furthermore, molecular docking simulations demonstrated that SD (the most potent PL inhibitor from Cortex Mori Radicis) could create strong interaction with Ser152 (the key amino acid in the catalytic triad) of PL via hydrogen bonding. All these findings provided a new powerful evidence for explaining the hypolipidemic effect of Cortex Mori Radicis, also suggested that some abundant natural compounds in this herbal medicine could be served as lead compounds for the development of new PL inhibitors.
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