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甘草叶中苯丙素二氢查耳酮和黄酮的结构及体外抗肝纤维化活性

Structures and In Vitro Antihepatic Fibrosis Activities of Prenylated Dihydrostilbenes and Flavonoids from Glycyrrhiza uralensis Leaves.

机构信息

State Key Laboratory of Reproductive Regulation and Breeding of Grassland Livestock; Key Laboratory of Forage and Endemic Crop Biotechnology, Ministry of Education; School of Life Sciences, Inner Mongolia University, Hohhot, P.R. China.

出版信息

J Food Sci. 2019 May;84(5):1224-1230. doi: 10.1111/1750-3841.14592. Epub 2019 Apr 16.

DOI:10.1111/1750-3841.14592
PMID:30990886
Abstract

Glycyrrhiza uralensis is the major plant source of licorice. This study was to identify bioactive compounds from the plant's leaves in order to make better use of its aerial part. An ethanol extract of the leaves was subjected to repeated chromatography to yield 15 compounds. The structures were determined to be three novel dihydrostilbenes, based on their various spectroscopic data-glycypytilbene A (1), glycydipytilbene (2), and glycypytilbene B (3)-and 12 known compounds, α,α'-dihydro-3,5,4'-trihydroxy-4,3'-diisopentenylstilbene (4), α,α'-dihydro-3,5,3',4'-tetrahydroxy-2,5'-diisopentenylstilbene (5), 6-prenyleriodictyol (6), 5'-prenyleriodictyol (7), 6-prenylquercetin-3-Me ether (8), 5'-prenylquercetin (9), 6-prenylquercetin (10), 6-prenylnaringenin (11), 3'-prenylnaringenin (12), sigmoidin C (13), 8-[(E)-3-hydroxymethyl-2- butenyl]-eriodictyol (14), and quercetin-3-Me ether (15). Most of these chemical constituents inhibited α-glucosidase activity, with the two prenylated quercetin derivatives (9 to 10) being the greatest active (IC < 4.0 µg/mL). Compounds 1, 3 to 4, 6 to 7, 9 to 12 impeded the growth of human hepatic stellate cells, with the prenylated flavonoids (6 to 7, 9 to 12) being more robust than their unprenylated counterparts. PRACTICAL APPLICATIONS: This study found that Glycyrrhiza uralensis leaves contain prenylated dihydrostilbenes and flavonoids with inhibiting effects on α-glucosidase and on the proliferation of human hepatic stellate cells, which should prompt the development of G. uralensis leaves for healthy products with anti-diabetic or liver fibrosis-preventing effects.

摘要

胀果甘草是甘草的主要植物来源。本研究旨在从其叶片中鉴定生物活性化合物,以更好地利用其地上部分。将叶片的乙醇提取物进行反复层析,得到 15 种化合物。根据其各种光谱数据,将这些化合物确定为三种新型二氢二苯乙烯,即甘草吡汀 A(1)、甘草二吡汀(2)和甘草吡汀 B(3),以及 12 种已知化合物,α,α'-二氢-3,5,4'-三羟基-4,3'-二异戊烯基二苯乙烯(4)、α,α'-二氢-3,5,3',4'-四羟基-2,5'-二异戊烯基二苯乙烯(5)、6-prenyleriodictyol(6)、5'-prenyleriodictyol(7)、6-prenylquercetin-3-Me ether(8)、5'-prenylquercetin(9)、6-prenylquercetin(10)、6-prenylnaringenin(11)、3'-prenylnaringenin(12)、sigmoidin C(13)、8-[(E)-3-羟甲基-2-丁烯基]-eriodictyol(14)和 quercetin-3-Me ether(15)。这些化学成分大多抑制α-葡萄糖苷酶活性,两个prenylated quercetin 衍生物(9 至 10)的活性最强(IC < 4.0 µg/mL)。化合物 1、3 至 4、6 至 7、9 至 12 抑制人肝星状细胞的生长,prenylated flavonoids(6 至 7、9 至 12)比其 unprenylated counterparts 更为有效。实际应用:本研究发现,胀果甘草叶片含有抑制α-葡萄糖苷酶和人肝星状细胞增殖的prenylated 二氢二苯乙烯和类黄酮,这应该促使开发具有抗糖尿病或预防肝纤维化作用的健康产品。

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