假鸢尾鳞茎胆碱酯酶抑制剂的分离与鉴定。

D. Sevim, B. Şener
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引用次数: 2

摘要

大多数球茎植物除了具有观赏价值外,还具有药用价值。土耳其是许多美丽球茎植物的发源地之一。为了继续从土耳其药用植物中寻找新的天然胆碱酯酶抑制剂的广泛研究,本研究研究了鸢尾L.物种的体外胆碱酯酶抑制作用,旨在评估胆碱酯酶抑制剂对乙酰胆碱酯酶(AChE)和丁基胆碱酯酶(BChE)的活性以及抗氧化能力,以及它们的神经保护潜力。采用改进的Ellmann法对47个鸢尾属植物球茎的二氯甲烷和甲醇提取物进行筛选,结果表明,鸢尾属植物球茎甲醇提取物对丁基胆碱酯酶的抑制作用最高,对鸢尾属植物甲醇提取物进行生物活性引导分离得到的二氯甲烷亚提取物对丁基胆碱酯酶的抑制活性为73.65±2.06%。这些活性亚提取物经柱层析分离得到6个馏分。编码为N5的组分对丁基胆碱酯酶的抑制活性(93.78±1.49%)显著高于加兰他敏(80.02±0.12%)。快闪色谱法对N5进行分馏,鉴定出编码为DS-5的亚组分对丁酰胆碱酯酶的抑制活性最高,为94.00±1.03%。采用LC-ESI-Q/TOF-MS-MS技术对其质量数据进行分析,鉴定其活性成分为伊里斯酮葡萄糖吡喃苷。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Isolation and Identification of Cholinesterase Inhibitors from the Bulbs of Iris pseudacorus L.
Most of the bulbous plants are known for their medicinal purposes in addition to their ornamental value. Turkey is one of the home country of many beautiful bulbous plants. In continuation of our extensive studies on finding new natural cholinesterase inhibitors from Turkish medicinal plants, Iris L. species were investigated for their in vitro cholinesterase inhibitory effects designed to assess cholinesterase inhibitor activities on both acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) and antioxidant capacities with respect to their neuroprotective potential in this study. The dichloromethane and methanol extracts prepared from the bulbs of 47 Iris taxa were screened by using modified Ellmann method and the highest butyrylcholinesterase inhibitory effect was found in the methanol extract of the bulbs of Iris pseudacorus L. The dichloromethane sub-extract, which is obtained bioactivity-guided fractionation of methanol extract of I. pseudacorus L., was exhibited significant butyrylcholinesterase inhibitory activity (73.65 ± 2.06 %). These active sub-extract was subjected to fractionation on column chromatography and obtained six fractions. Among the fractions, coded as N5 was shown the significant butyrylcholinesterase inhibitory activity (93.78 ± 1.49 %) compared with galanthamine (80.02 ± 0.12 %). Fractionation of N5 on flash chromatography the highest butyrylcholinesterase inhibitory activity of sub-fraction coded as DS-5 was determined as 94.00 ± 1.03 %. The responsible compound from the activity of this sub-fraction was detected as irisolidone glucopyranoside based on its mass data by using LC-ESI-Q/TOF-MS-MS technique.
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