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首页> 外文期刊>Archives of pharmacal research >Evaluation of the inhibitory effects of eckol and dieckol isolated from edible brown alga Eisenia bicyclis on human monoamine oxidases A and B
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Evaluation of the inhibitory effects of eckol and dieckol isolated from edible brown alga Eisenia bicyclis on human monoamine oxidases A and B

机译:从食用棕榈藻藻藻素氧化酶A和B中食用棕榈藻藻藻酸纤维素患者抑制作用的评价

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摘要

Eckol and dieckol are important phlorotannins found in edible brown algae including Eisenia bicyclis, Ecklonia stolonifera, and others. Inhibition of monoamine oxidase (MAO) play an important role in the early management of Parkinson's disease (PD). The aim of this study was to determine the effectiveness of eckol and dieckol isolated from the methanolic extract of E. bicyclis against PD by the inhibition of human MAO-A and MAO-B (hMAO-A and hMAO-B). A sensitive enzyme-based chemiluminescent assay and kinetics methods were used to investigate enzyme inhibition and mode of inhibition. A molecular docking simulation was performed to clarify the binding characteristics of eckol and dieckol to hMAO-A and hMAO-B. The results suggested that methanolic extract of E. bicyclis and its isolated phlorotannins, eckol and dieckol, have potent inhibitory activity against hMAO-A and hMAO-B. The enzyme-based kinetics results demonstrated eckol mixed and non-competitive inhibition of hMAO-A and hMAO-B, respectively, while dieckol non-competitively inhibited both hMAOs. Molecular docking simulation predicted that eckol and dieckol exhibit higher binding affinity towards hMAO-A and hMAO-B through hydrogen bonding and hydrophobic interactions. These findings implicate eckol and dieckol as inhibitors of hMAOs that might be of potential value in the management of PD.
机译:Eckol和Dieckol是一种重要的phlorotannins,其在食用棕海藻类中发现,包括艾西哥肾上腺,Ecklonia Stolonifera等。抑制单胺氧化酶(MAO)在帕金森病(PD)的早期管理中发挥着重要作用。本研究的目的是通过抑制人Mao-A和MaO-B(HMAO-A和HMAO-B),确定从E.甲醇提取物中分离的Eckol和Dieckol的有效性。使用敏感的基于酶的化学发光测定和动力学方法来研究酶抑制和抑制模式。进行分子对接模拟以阐明HMAO-A和HMAO-B的Eckol和Dieckol的结合特征。结果表明,E. BiCyclis及其分离的植物分离的甲醇提取物,Eckol和Dieckol,对HMAO-A和HMAO-B具有有效的抑制活性。基于酶的动力学结果分别显示出HMAO-A和HMAO-B的Eckol混合和非竞争抑制,而Dieckol无竞争性地抑制HMAOS。分子对接模拟预测,Eckol和Dieckol通过氢键和疏水相互作用对HMAO-A和HMAO-B具有更高的结合亲和力。这些发现将Eckol和Dieckol称为HMAOS的抑制剂,其可能具有PD管理中的潜在价值。

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