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从L.叶中分离出的毛蕊花糖苷通过其酶抑制和自由基清除能力所具有的神经保护潜力。

Neuroprotective Potential of Verbascoside Isolated from L. Leaves through Its Enzymatic Inhibition and Free Radical Scavenging Ability.

作者信息

Burgos Carmen, Muñoz-Mingarro Dolores, Navarro Inmaculada, Martín-Cordero Carmen, Acero Nuria

机构信息

Department of Pharmacology, Faculty of Pharmacy, Seville University, C/P. García González s/n, 41012 Seville, Spain.

Chemistry and Biochemistry Department, San Pablo-CEU University, CEU Universities, Urb. Montepríncipe, 28668 Boadilla del Monte, Madrid, Spain.

出版信息

Antioxidants (Basel). 2020 Nov 30;9(12):1207. doi: 10.3390/antiox9121207.

Abstract

The phenomenon of today's ageing population has increased interest in the search for new active substances that delay the onset and development of neurodegenerative diseases. In this respect, the search for natural compounds, mainly phenolic compounds, with neuroprotective activity has become the focus of growing interest. Verbascoside is a phenylethanoid that has already presented several pharmacological activities. The purpose of this study is to isolate and identify verbascoside from leaves. Consequently, its neuroprotective ability through enzymatic inhibition and free radical scavenging ability has been analyzed both in vitro and in cell culture assays. The antioxidant capacity of verbascoside was evaluated in vitro through total antioxidant capacity, DPPH•, OH•, and O2•-scavenging activity assays. The effect of verbascoside on intracellular reactive oxygen species (ROS) levels of HepG2 and SH-SY5Y cell lines was studied in normal culture and under induced oxidative stress. The inhibitory ability of the phenylethanoid against several enzymes implied in neurodegenerative diseases (tyrosinase, MAO-A, and AChE) was analyzed in vitro. Verbascoside neuroprotective activity is at least in part related to its free radical scavenging ability. The effect of verbascoside on ROS production suggests its potential in the prevention of harmful cell redox changes and in boosting neuroprotection.

摘要

当今人口老龄化现象使得人们对寻找能够延缓神经退行性疾病发病和发展的新活性物质的兴趣增加。在这方面,寻找具有神经保护活性的天然化合物,主要是酚类化合物,已成为越来越受关注的焦点。毛蕊花糖苷是一种苯乙醇苷类化合物,已表现出多种药理活性。本研究的目的是从叶片中分离和鉴定毛蕊花糖苷。因此,已在体外和细胞培养试验中分析了其通过酶抑制和自由基清除能力的神经保护能力。通过总抗氧化能力、DPPH•、OH•和O2•-清除活性试验在体外评估了毛蕊花糖苷的抗氧化能力。在正常培养和诱导氧化应激条件下,研究了毛蕊花糖苷对HepG2和SH-SY5Y细胞系细胞内活性氧(ROS)水平的影响。在体外分析了该苯乙醇苷类化合物对几种与神经退行性疾病相关的酶(酪氨酸酶、单胺氧化酶A和乙酰胆碱酯酶)的抑制能力。毛蕊花糖苷的神经保护活性至少部分与其自由基清除能力有关。毛蕊花糖苷对ROS产生的影响表明其在预防有害细胞氧化还原变化和增强神经保护方面的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9538/7759776/fca4d5538b48/antioxidants-09-01207-g001.jpg

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