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首页> 外文期刊>Fisheries Science >Acetyl- and butyrylcholinesterase inhibitory activities of sterols and phlorotannins from Ecklonia stolonifera
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Acetyl- and butyrylcholinesterase inhibitory activities of sterols and phlorotannins from Ecklonia stolonifera

机译:东方ck的固醇和苯单宁的乙酰和丁酰胆碱酯酶抑制活性

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摘要

As part of this study on the isolation of cholinesterase inhibitors from natural marine products, the bioactivity of the ethanolic extracts from 27 Korean seaweeds were screened using acetylcholinesterase (AChE) and butyrylcholine sterase (BChE) inhibitory assays. Ecklonia stolonifera exhibited promising inhibitory properties against both AChE and BChE. Bioassay-guided fractionation of the active n-hexane and ethyl acetate (EtOAc) soluble fractions, obtained from the ethanolic extract of E. stolonifera, resulted in the isolation of the sterols; fucosterol (1) and 24-hydroperoxy 24-vinylcholesterol (2), from the n-hexane fraction and the phlorotannins; phloroglucinol (3), ecks-tolonol (4), eckol (5), phlorofucofuroeckol-A (6), dieckol (7), triphlorethol-A (8), 2-phloroeckol (9) and 7-phloroeckol (10), from the EtOAc fraction. Of these, compounds 2, 9 and 10 were isolated from E. stolonifera for the first time. Compounds 4–7, 9 and 10 exhibited inhibitory potential against AChE, with 50% inhibition concentration (IC50) values of 42.66±8.48, 20.56±5,61, 4.89±2.28, 17.11±3.24, 38.13±4.95 and 21.11±4.16 μM, respectively; whereas, compounds 1, 2, 4 and 6 were found to be active against BChE, with IC50 values of 421.72±1.43, 176.46±2.51, 230.27±3.52 and 136.71±3.33 μM, respectively. It has been suggested that the inhibition of these enzymes by the sterols and phlorotannins derived from marine brown algae could be a useful approach for the treatment of Alzheimer’s disease.
机译:作为从天然海产品中分离胆碱酯酶抑制剂的研究的一部分,使用乙酰胆碱酯酶(AChE)和丁酰胆碱酯酶(BChE)抑制试验筛选了27种韩国海藻的乙醇提取物的生物活性。东方无花果对AChE和BChE均显示出有希望的抑制特性。生物测定指导下的活性成分正己烷和乙酸乙酯(EtOAc)可溶性馏分的分离,得自stolonifera的乙醇提取物,可分离出甾醇。来自正己烷馏分和间苯三酚的富烯甾醇(1)和24-氢过氧24-乙烯基胆固醇(2);间苯三酚(3),eck-tolonol(4),eckol(5),phlorofucofuroeckol-A(6),dieckol(7),triphlorethol-A(8),2-phroroeckol(9)和7-phloroeckol(10),来自EtOAc馏分。其中,化合物2、9和10首次从stolonifera中分离出来。化合物4-7、9和10表现出对AChE的抑制潜能,其50%抑制浓度(IC50 )值为42.66±8.48、20.56±5,61、4.89±2.28、17.11±3.24、38.13±4.95和分别为21.11±4.16μM;而化合物1、2、4和6对BChE具有活性,IC50值分别为421.72±1.43、176.46±2.51、230.27±3.52和136.71±3.33μM。有人提出,源自海洋褐藻的固醇和邻单宁抑制这些酶可能是治疗阿尔茨海默氏病的有用方法。

著录项

  • 来源
    《Fisheries Science》 |2008年第1期|200-207|共8页
  • 作者单位

    Division of Food Science and Biotechnology Pukyong National University 608-737 Busan Japan;

    College of Pharmacy Pusan National University 609-735 Busan Republic of Korea;

    Division of Food Science and Biotechnology Pukyong National University 608-737 Busan Japan;

    Division of Food Science and Biotechnology Pukyong National University 608-737 Busan Japan;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    chollnesterase inhibition; Ecklonia stolonifera; phlorotannins; seaweeds; sterols;

    机译:胆甾醇酯酶抑制作用;埃克罗氏菌;芦丁单宁;海藻;甾醇;

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