Identification, characterisation, and quantification of phenolic compounds in the antioxidant activity-containing fraction from the seeds of Korean perilla (Perilla frutescens) cultivars

被引:134
作者
Lee, Jin Hwan [1 ]
Park, Ki Hun [2 ]
Lee, Myoung-Hee [3 ]
Kim, Hyun-Tae [3 ]
Seo, Woo Duck [3 ]
Kim, Jun Young [3 ]
Baek, In-You [3 ]
Jang, Dae Sik [4 ]
Ha, Tae Joung [3 ]
机构
[1] Minist Environm, NAKDONG River Basin Environm Off, Dept Monitoring & Anal, Chang Won 641722, South Korea
[2] GyeongSang Natl Univ, IALS, Div Appl Life Sci, BK21 Program, Jinju 660751, South Korea
[3] Rural Dev Adm, NICS, Dept Funct Crop, Miryang 627803, South Korea
[4] Kyung Hee Univ, Coll Pharm, Dept Pharmaceut Sci, Seoul 130701, South Korea
关键词
Perilla seed; Phenolic compound; UPLC-PDA-ESI/MS; NMR; Antioxidant activity; Cultivar; ACID; GRAINS; LEAVES; L;
D O I
10.1016/j.foodchem.2012.08.057
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The present research was the first to investigate phenolic compound profiles and antioxidant properties in the seeds of various perilla (Perilla frutescens) cultivars. The 80% methanol extract (50 mu g/ml) of this species showed potent antioxidant activities against 2,2-diphenyl-1-picrylhydrazyl (DPPH) and 2,2'-azino-bis(3-ethylbenzthiazoline-6-sulphonic acid) (ABTS) radicals. Phenolic compounds were characterised by nuclear magnetic resonance (NMR) spectroscopy, and ultra performance liquid chromatography with photodiode array detector and electrospray ionisation/mass (UPLC-PDA-ESI/MS) analysis. Nine compounds were elucidated as caffeic acid-3-O-glucoside (1), caffeic acid (2), luteolin-7-O-glucoside (3), apigenin-7-O-glucoside (4), rosmarinic acid-3-O-glucoside (5), rosmarinic acid (6), luteolin (7), apigenin (8), and chrysoeriol (9). The individual and total phenolic contents were remarkably different, especially rosmarinic acid-3-O-glucoside (5) and rosmarinic acid (6) which were the predominant compounds (>95%) in all perilla cultivars. Additionally, Yeupsil cultivar exhibited the highest phenolic content (5029.0 mu g/g) and antioxidant activity, whereas the lowest was shown by Dasil (2138.7 mu g/g). Therefore, these results suggest that antioxidant effects of perilla seeds are correlated with phenolic contents. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:843 / 852
页数:10
相关论文
共 30 条
[1]   Antidiabetic activity of phenolic compounds from Pecan bark in streptozotocin-induced diabetic rats [J].
Abdallah, Hossam M. ;
Salama, Maha M. ;
Abd-Elrahman, Enas H. ;
El-Maraghy, Shohda A. .
PHYTOCHEMISTRY LETTERS, 2011, 4 (03) :337-341
[2]   Use of HPLC-DAD-ESI/MS to profile phenolic compounds in edible wild greens from Portugal [J].
Barros, Lillian ;
Duenas, Montserrat ;
Ferreira, Isabel C. F. R. ;
Carvalho, Ana Maria ;
Santos-Buelga, Celestino .
FOOD CHEMISTRY, 2011, 127 (01) :169-173
[3]   Antioxidant capacities and phenolic compounds of the husk, bran and endosperm of Thai rice [J].
Butsat, Sunan ;
Siriamornpun, Sirithon .
FOOD CHEMISTRY, 2010, 119 (02) :606-613
[4]   Bioaccessibility and antioxidant potential of millet grain phenolics as affected by simulated in vitro digestion and microbial fermentation [J].
Chandrasekara, Anoma ;
Shahidi, Fereidoon .
JOURNAL OF FUNCTIONAL FOODS, 2012, 4 (01) :226-237
[5]   Determination of antioxidant activity in free and hydrolyzed fractions of millet grains and characterization of their phenolic profiles by HPLC-DAD-ESI-MSn [J].
Chandrasekara, Anoma ;
Shahidi, Fereidoon .
JOURNAL OF FUNCTIONAL FOODS, 2011, 3 (03) :144-158
[6]   Dietary perilla oil lowers serum lipids and ovalbumin-specific IgG1, but increases total IgE levels in ovalbumin-challenged mice [J].
Chang, Hui-Hsiang ;
Chen, Chin-Shuh ;
Lin, Jin-Yuarn .
FOOD AND CHEMICAL TOXICOLOGY, 2009, 47 (04) :848-854
[7]   Antioxidant activity of methanolic extracts from some grains consumed in Korea [J].
Choi, Youngmin ;
Jeong, Heon-Sang ;
Lee, Junsoo .
FOOD CHEMISTRY, 2007, 103 (01) :130-138
[8]   UPLC-PDA-MS evaluation of bioactive compounds from leaves of Ilex paraguariensis with different growth conditions, treatments and ageing [J].
Dartora, Nessana ;
de Souza, Lauro M. ;
Santana-Filho, Arquimedes P. ;
Iacomini, Marcello ;
Valduga, Alice T. ;
Gorin, Philip A. J. ;
Sassaki, Guilherme L. .
FOOD CHEMISTRY, 2011, 129 (04) :1453-1461
[9]   Phenolic acid derivatives with potential anticancer properties - a structure-activity relationship study. Part 1: Methyl, propyl and octyl esters of caffeic and gallic acids [J].
Fiuza, SM ;
Gomes, C ;
Teixeira, LJ ;
da Cruz, MTG ;
Cordeiro, MNDS ;
Milhazes, N ;
Borges, F ;
Marques, MPM .
BIOORGANIC & MEDICINAL CHEMISTRY, 2004, 12 (13) :3581-3589
[10]   Isolation and identification of phenolic compounds from the seeds of Perilla frutescens (L.) and their inhibitory activities against α-glucosidase and aldose reductase [J].
Ha, Tae Joung ;
Lee, Jin Hwan ;
Lee, Myoung-Hee ;
Lee, Byeong Won ;
Kwon, Hyun Sook ;
Park, Chang-Hwan ;
Shim, Kang-Bo ;
Kim, Hyun-Tae ;
Baek, In-Youl ;
Jang, Dae Sik .
FOOD CHEMISTRY, 2012, 135 (03) :1397-1403