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骨碎补中乙酰胆碱酯酶抑制剂的生物导向分离与结构鉴定

Bioguided Isolation and Structure Identification of Acetylcholinesterase Enzyme Inhibitors from Drynariae Rhizome.

作者信息

Liu Ming-Yang, Zeng Fan, Shen Yue, Wang Yu-Ying, Zhang Ning, Geng Fang

机构信息

Key Laboratory of Photochemistry Biomaterials and Energy Storage Materials of Heilongjiang Province, College of Chemistry & Chemical Engineering, Harbin Normal University, Harbin 150025, China.

College of Jiamusi, Heilongjiang University of Chinese Medicine, Jiamusi, Harbin, Heilongjiang 154007, China.

出版信息

J Anal Methods Chem. 2020 Feb 23;2020:2971841. doi: 10.1155/2020/2971841. eCollection 2020.

Abstract

Drynariae Rhizome, widely distributed in southern China, was clinically used as a traditional treatment for cognitive disfunction, such as Alzheimer's disease (AD). The aim of our work was to evaluate the AChE inhibition activities of extracts of Drynariae Rhizome and pure compounds using a bioguided fractionation procedure. The classical approach for screening potential AChE inhibitors was developed by Ellman. However, the background color of compounds or herb extracts remained uncertain and frequently interfered with the detection of the secondary reaction, thereby easily yielding false positive or false negative results. Here, a high-throughput assay monitoring the transformation of iodized choline from iodized acetylcholine catalyzed by AChE was established based on UPLC-MS/MS. The bioguided fractionation of the extract using this method resulted in the isolation of eight AChE inhibitory flavonoids, including naringenin, eriodictyol, kaempferol, luteolin, astragalin, luteolin-7-O--D-glucoside, naringin, and neoeriocitrin, with the IC values of 3.81 ± 0.21 M, 7.19 ± 0.62 M, 11.09 ± 1.02 M, 17.26 ± 0.23 M, 18.24 ± 2.33 M, 17.13 ± 1.02 M, 26.4 ± 1.17 M, and 22.49 ± 1.25 M. It is assumed that the identified flavonoids contribute to the AChE inhibition activity of Drynariae Rhizome. These results are in agreement with the traditional uses of Drynariae Rhizome for AD.

摘要

骨碎补广泛分布于中国南方,在临床上被用作治疗认知功能障碍(如阿尔茨海默病,AD)的传统药物。我们研究的目的是采用生物活性追踪分离法评估骨碎补提取物和纯化合物的乙酰胆碱酯酶(AChE)抑制活性。Ellman开发了筛选潜在AChE抑制剂的经典方法。然而,化合物或草药提取物的背景颜色仍不确定,经常干扰二级反应的检测,从而容易产生假阳性或假阴性结果。在此,基于超高效液相色谱-串联质谱(UPLC-MS/MS)建立了一种监测AChE催化碘化乙酰胆碱转化为碘化胆碱的高通量检测方法。使用该方法对提取物进行生物活性追踪分离,得到了8种具有AChE抑制活性的黄酮类化合物,包括柚皮素、圣草酚、山奈酚、木犀草素、紫云英苷、木犀草素-7-O-β-D-葡萄糖苷、柚皮苷和新橙皮苷,其半数抑制浓度(IC)值分别为3.81±0.21μM、7.19±0.62μM、11.09±1.02μM、17.26±0.23μM、18.24±2.33μM、17.13±1.02μM、26.4±1.17μM和22.49±1.25μM。据推测,所鉴定的黄酮类化合物是骨碎补具有AChE抑制活性的原因。这些结果与骨碎补治疗AD的传统用途相符。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8cc/7059089/55759ce7165f/JAMC2020-2971841.001.jpg

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