Isolation and identification of phenolic compounds from the seeds of Perilla frutescens (L.) and their inhibitory activities against α-glucosidase and aldose reductase

被引:207
作者
Ha, Tae Joung [1 ]
Lee, Jin Hwan [2 ]
Lee, Myoung-Hee [1 ]
Lee, Byeong Won [1 ]
Kwon, Hyun Sook [1 ]
Park, Chang-Hwan [1 ]
Shim, Kang-Bo [1 ]
Kim, Hyun-Tae [1 ]
Baek, In-Youl [1 ]
Jang, Dae Sik [3 ]
机构
[1] Rural Dev Adm, Dept Funct Crop, Natl Inst Crop Sci, Miryang 627803, South Korea
[2] Minist Environm, Dept Monitoring & Anal, NAKDONG River Basin Environm Off, Chang Won 641722, Gyeongnam, South Korea
[3] Kyung Hee Univ, Dept Pharmaceut Sci, Coll Pharm, Seoul 130701, South Korea
关键词
Perilla fnitescens; Seeds; alpha-Glucosidase; Human aldose reductase; Luteolin; Rosmarinic acid; LEAVES;
D O I
10.1016/j.foodchem.2012.05.104
中图分类号
O69 [应用化学];
学科分类号
070301 [无机化学];
摘要
Five phenolic compounds were isolated from the seeds of Perilla (Perilla frutescens L) using gradient solvent fractionation, silica gel column chromatography, and preparative high-performance liquid chromatography (HPLC). Their chemical structures were identified as caffeic acid-3-O-glucoside (1), rosmarinic acid-3-O-glucoside (2), rosmarinic acid (3), luteolin (4), and apigenin (5) using NMR spectroscopy and HPLC-ESI/MS analysis. Among them, luteolin (4) inhibited alpha-glucosidase (EC 3.2.1.20) with IC50 value of 45.4 mu M. The inhibition kinetic analysed by Dixon plot indicate that luteolin is a noncompetitive inhibitor, and the inhibition constant K-1 was calculated at 45.0 mu M. Moreover, rosmarinic acid (3) and luteolin (4) inhibited recombinant human aldose reductase (EC 1.1.1.21) with IC50 values of 11.2 and 0.6 mu M, respectively. Notably, the inhibition kinetic of luteolin (4) follows a hyperbolic dependence on aldose reductase inhibition by Dixon plot. Thus, inhibition kinetic indicates that luteolin (4) is a mixed-type inhibitor. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1397 / 1403
页数:7
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