首页> 外文期刊>Phytochemistry Letters >An in vitro and in silico approach to cholinesterase inhibitory and antioxidant effects of the methanol extract, furanocoumarin fraction, and major coumarins of Angelica officinalis L fruits
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An in vitro and in silico approach to cholinesterase inhibitory and antioxidant effects of the methanol extract, furanocoumarin fraction, and major coumarins of Angelica officinalis L fruits

机译:一种体外和计算机模拟的方法,对当归甲醇提取物的甲醇提取物,呋喃香豆素组分和主要香豆素具有胆碱酯酶抑制和抗氧化作用

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Cholinesterase inhibitory and antioxidant activities of the methanol extract, furanocoumarin fraction, and major coumarins (imperatorin, xanthotoxin, and bergapten) of the fruits of Angelica officinalis L. growing in Poland were determined in the current study. Cholinesterase inhibition was tested against acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) at 12.5, 25, 50, and 100 mu gmL~(-1) using EL1SA microplate reader. Antioxidant activity of the samples was tested by in vitro models including radical scavenging activity against 2,2-diphenyl-l -picrylhydrazyl (DPPH), N.N-dimethyl-p-phenylen-diamine (DMPD) as well as ferrous ion-chelation capacity, ferric-(FRAP) and phosphomolibdenum-reducing antioxidant power (PRAP) assays at 500, 1000,and 2000 mu g mL~(-1). The extract was found to have strong inhibition against BChE (85.65 ± 1.49%) and low inhibition against AChE (27.49 ± 2.01%) at 100 u gmL~(-1). Four major coumarins; imperatorin, isoimperatorin, xanthotoxin, and bergapten were identified in the extract by HPLC. Imperatorin (83.98 ± 0.99%), xanthotoxin (88.04 ± 0.83%), and bergapten (86.69 ± 2.56%) displayed strong inhibition towards BChE. Molecular docking studies confirmed potent interactions between BChE and the tested furanocoumarins. The samples did not possess radical scavenging activity against DPPH and DMPD, whereas they possessed a moderate level of FRAP and PRAP at the tested concentrations. To the best of our knowledge, the current work constitutes the first studyon cholinesterase inhibitory and antioxidant activities of A. officinalis.
机译:在本研究中,测定了当归在波兰生长的当归果实中的甲醇提取物,呋喃香豆素部分和主要香豆素(欧前胡素,黄腐毒素和佛手柑)的胆碱酯酶抑制和抗氧化活性。使用EL1SA微孔板读板器在12.5、25、50和100μgmL〜(-1)下测试了对乙酰胆碱酯酶(AChE)和丁酰胆碱酯酶(BChE)的胆碱酯酶抑制作用。通过体外模型测试了样品的抗氧化活性,其中包括对2,2-二苯基-1-甲基水合肼(DPPH),NN-二甲基-对苯二胺(DMPD)的自由基清除活性以及亚铁离子螯合能力,分别在500、1000和2000μg mL〜(-1)下进行三价铁(FRAP)和磷钼还原抗氧化剂能力(PRAP)测定。在100 u gmL〜(-1)时,提取物对BChE的抑制作用强(85.65±1.49%),对AChE的抑制作用低(27.49±2.01%)。四种主要香豆素;高效液相色谱法鉴定了提取物中的欧前胡素,异欧前胡素,黄嘌呤毒素和佛手柑。 Imperatorin(83.98±0.99%),黄腐毒素(88.04±0.83%)和bergapten(86.69±2.56%)对BChE表现出强烈的抑制作用。分子对接研究证实了BChE与测试的呋喃香豆素之间有力的相互作用。样品不具有针对DPPH和DMPD的自由基清除活性,而它们在测试浓度下具有中等水平的FRAP和PRAP。据我们所知,目前的工作构成了首次对A. officinalis的胆碱酯酶抑制和抗氧化活性的研究。

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