Suppr超能文献

黄独 Scrophularia flava Grau 中的一种三糖苯乙醇苷具有通过抑制 α-葡萄糖苷酶和降低氧化应激来防治 2 型糖尿病的潜力。

A trisaccharide phenylethanoid glycoside from Scrophularia flava Grau with potential anti-type 2 diabetic properties by inhibiting α-glucosidase enzyme and decreasing oxidative stress.

机构信息

Medicinal Plants Processing Research Center, Shiraz University of Medical Sciences, Shiraz, Iran; Department of Pharmacognosy, School of Pharmacy, Shiraz University of Medical Sciences, Shiraz, Iran.

Medicinal Plants Processing Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.

出版信息

Bioorg Chem. 2020 Jun;99:103776. doi: 10.1016/j.bioorg.2020.103776. Epub 2020 Apr 1.

Abstract

The Scrophularia genus is a rich source of phenylethanoid glycosides, with diverse biological activities including anti-diabetic properties. This study investigated anti-type 2 diabetic potential and active component of Scrophularia flava Grau. A new phenylethanoid glycoside was isolated from aerial parts of the plant and identified as 2-(4-hydroxy-3-methoxyphenyl) ethyl 6-deoxy-3-O-[(2E)-3-(3 hydroxy-4-methoxyphenyl) prop-2-enoyl]-α-rhamnopyranosyl-(1 → 3)-[α-rhamnopyranosyl-(1 → 6)]-4-O-[(2E)-3-(4-hydroxy-3-methoxyphenyl) prop-2-enoyl]-β-glucopyranoside. It was named flavaioside. The structure of flavaioside was identified based on H NMR, C NMR, DEPT-HSQC, COSY, HMBC, NOESY and LC-ESI-MS-MS. Total methanol extract, fractions (A-F) and specific main phenylethanoid glycoside (flavaioside), were assessed for inhibitory effects against the α-glucosidase enzyme (in vitro anti-type 2 diabetic assay). The antioxidant activities of methanol extracts, all fractions and isolated flavaioside were identified based on 2, 2'-diphenyl-1-picrylhydrazyl radical (DPPH) scavenging activity, 2, 2'-azino-bis (3-ethylbenzothiazoline)-6-sulphonic acid radical cation (ABTS) scavenging activity, phosphomolybdenum method, and metal chelating activity. In comparison to the other fractions, the best antioxidant result was observed in fraction E and its main compound, flavaioside, in DPPH (IC = 4.26, 2.57 µg/mL) and ABTS (EC = 55.45, 6.34 µg/mL) scavenging activities. Flavaioside showed significantly stronger activities than α-tocopherol and ascorbic acid in DPPH and ABTS assays. Furthermore, flavaioside showed a potent inhibitory activity on the α-glucosidase enzyme which was comparable with the known anti-type 2 diabetic drug, acarbose (91.85%, and 92.87%, respectively). Fraction E and flavaioside showed α-glucosidase inhibitory activities with IC values, 65.05 and 6.50 µg/mL. The plant and its isolated flavaioside can possess acceptable anti-type 2 diabetic potential and anti-oxidant activity.

摘要

玄参科是苯乙醇苷类化合物的丰富来源,具有多种生物活性,包括抗糖尿病特性。本研究调查了玄参的抗 2 型糖尿病潜力及其活性成分。从植物的地上部分分离得到一种新的苯乙醇苷,并鉴定为 2-(4-羟基-3-甲氧基苯基)乙基 6-去氧-3-O-[(2E)-3-(3 羟基-4-甲氧基苯基)丙烯酰基]-α-鼠李吡喃糖苷基-(1→3)-[α-鼠李吡喃糖苷基-(1→6)]-4-O-[(2E)-3-(4-羟基-3-甲氧基苯基)丙烯酰基]-β-吡喃葡萄糖苷。它被命名为 flavaioside。根据 1H NMR、13C NMR、DEPT-HSQC、COSY、HMBC、NOESY 和 LC-ESI-MS-MS 确定 flavaioside 的结构。总甲醇提取物、馏分(A-F)和特定的主要苯乙醇苷(flavaioside)被评估对α-葡萄糖苷酶(体外抗 2 型糖尿病测定)的抑制作用。根据 2,2'-二苯基-1-苦基肼基(DPPH)清除活性、2,2'-偶氮-双(3-乙基苯并噻唑啉-6-磺酸)自由基阳离子(ABTS)清除活性、磷钼酸盐法和金属螯合活性,确定甲醇提取物、所有馏分和分离的 flavaioside 的抗氧化活性。与其他馏分相比,在 DPPH(IC=4.26、2.57μg/mL)和 ABTS(EC=55.45、6.34μg/mL)清除活性方面,馏分 E 及其主要化合物 flavaioside 表现出最佳的抗氧化效果。Flavaioside 在 DPPH 和 ABTS 测定中比α-生育酚和抗坏血酸具有更强的活性。此外,flavaioside 对α-葡萄糖苷酶表现出较强的抑制活性,与已知的 2 型糖尿病药物阿卡波糖相当(分别为 91.85%和 92.87%)。馏分 E 和 flavaioside 的α-葡萄糖苷酶抑制活性的 IC 值分别为 65.05 和 6.50μg/mL。该植物及其分离的 flavaioside 具有可接受的抗 2 型糖尿病潜力和抗氧化活性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验