Evaluation of Antioxidant and Inhibitory Activities for Different Subclasses Flavonoids on Enzymes for Rheumatoid Arthritis

被引:139
作者
Lee, Je-Hyuk [1 ]
Kim, Gun-Hee [1 ,2 ]
机构
[1] Duksung Womens Univ, Plant Resources Res Inst, Seoul, South Korea
[2] Duksung Womens Univ, Dept Food & Nutr, Seoul, South Korea
关键词
collagenase; cyclooxygenase; flavonoid; hyaluronidase; lipoxygenase; NITRIC-OXIDE; CYCLOOXYGENASE-2; EXPRESSION; II COLLAGEN; CELLS; TISSUE; SPECTROSCOPY; INDUCTION; EXTRACT;
D O I
10.1111/j.1750-3841.2010.01755.x
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Antioxidant activities of flavonoids were decreased in the order of flavonols > flavanones > flavones. Inhibitory intensities for hyaluronidase and collagenase reaction differed clearly according to flavonoid subclasses. Kaempferol, quercetin, myricetin, and rutin in flavonols inhibited hyaluronidase reaction specifically, while apigenin, luteolin, baicalin, and baicalein in flavones showed specific inhibition to collagenase reaction. In addition, the flavonoids, except baicalin and catechin, inhibited potently LPS-induced nitrite production in a dose-dependent manner, which might be mainly due to the suppression of inducible nitric oxide (NO) synthase. Quercetin and luteolin showed the strongest inhibitory activities on 15-lipoxygenase (LOX), and quercetin showed relatively potent inhibition on cyclooxygenase-1 (COX-1) reaction. Otherwise, all tested flavonoids possessed the inhibitory activity to COX-2 reaction, and especially luteolin, kaempferol, hesperetin, and naringin showed relatively the potent inhibition on COX-2 reaction. This report elucidated the anti-inflammatory activities, such as the antioxidant property, inhibition of NO production, and inhibition of inflammatory enzymes (hyaluronidase, collagenase, LOX, and COXs) of several subclass flavonoids.
引用
收藏
页码:H212 / H217
页数:6
相关论文
共 33 条
[1]  
BABIOR BM, 1992, ADV ENZYMOL RAMB, V65, P49
[2]   Antioxidant and hepatoprotective effect of Acanthus ilicifolius [J].
Babu, BH ;
Shylesh, BS ;
Padikkala, J .
FITOTERAPIA, 2001, 72 (03) :272-277
[3]  
Cha J.Y., 2001, Appl. Biol. Chem, V44, P122
[4]  
Crofford LJ, 1997, J RHEUMATOL, V24, P15
[5]  
DAS DK, 1994, METHOD ENZYMOL, V234, P10
[6]  
Gordon MH, 1990, FOOD ANTIOXIDANTS, V1, P18, DOI DOI 10.1007/978-94-009-0753-9_1
[7]   Flavonoids as peroxynitrite scavengers: the role of the hydroxyl groups [J].
Heijnen, CGM ;
Haenen, GRMM ;
van Acker, FAA ;
van der Vijgh, WJF ;
Bast, A .
TOXICOLOGY IN VITRO, 2001, 15 (01) :3-6
[8]   Induction of COX-2 expression by nitric oxide in rheumatoid synovial cells [J].
Honda, S ;
Migita, K ;
Hirai, Y ;
Ueki, Y ;
Yamasaki, S ;
Urayama, S ;
Kawabe, Y ;
Fukuda, T ;
Kawakami, A ;
Kamachi, M ;
Kita, M ;
Ida, H ;
Aoyagi, T ;
Eguchi, K .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 268 (03) :928-931
[9]  
HUANG MT, 1991, CANCER RES, V51, P813
[10]  
Korhonen Riku, 2005, Current Drug Targets - Inflammation and Allergy, V4, P471, DOI 10.2174/1568010054526359