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桑白皮中新型胰腺脂肪酶抑制剂的天然成分。

Natural constituents from Cortex Mori Radicis as new pancreatic lipase inhibitors.

机构信息

Department of Biotechnology, College of Basic Medical Sciences, Dalian Medical University, Dalian 116044, China.

Institute of Interdisciplinary Medicine, Shanghai University of Traditional Chinese Medicine, Shanghai 201203, China; Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China.

出版信息

Bioorg Chem. 2018 Oct;80:577-584. doi: 10.1016/j.bioorg.2018.07.011. Epub 2018 Jul 17.

DOI:10.1016/j.bioorg.2018.07.011
PMID:30032067
Abstract

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 IC 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 K 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.

摘要

胰脂肪酶(PL)是一种在胃肠道中水解三酰甘油的关键酶,已被确定为调节脂质吸收的治疗靶点。在本研究中,从一种著名的中药桑白皮(中文名为桑白皮)中收集了六种主要成分,并通过荧光测定法仔细研究和充分表征了它们对 PL 的抑制作用。结果清楚地表明,从桑白皮中测试的所有生物活性成分,包括桑根酮 C(SC)、桑根酮 D(SD)、桑酮 C(KC)、桑酮 G(KG)、杨梅素和桑色素,均对 PL 具有强至中等的抑制作用,IC 值范围为 0.77μM 至 20.56μM。对抑制动力学的进一步研究表明,SC、SD、KC 和 KG 作为有效的混合抑制剂,对 PL 介导的 4-MU 油酸盐水解具有作用,K 值小于 5.0μM。此外,分子对接模拟表明,SD(桑白皮中最有效的 PL 抑制剂)可以通过氢键与 PL 的 Ser152(催化三联体中的关键氨基酸)形成强相互作用。所有这些发现为解释桑白皮的降血脂作用提供了新的有力证据,也表明该草药中一些丰富的天然化合物可能作为新型 PL 抑制剂的先导化合物。

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