In vitro peroxynitrite scavenging activity of diarylheptanoids from Curcuma longa

被引:60
作者
Kim, JE
Kim, AR
Chung, HY
Han, SY
Kim, BS
Choi, JS [1 ]
机构
[1] Pukyong Natl Univ, Fac Food Sci & Biotechnol, Pusan 608737, South Korea
[2] Pusan Natl Univ, Coll Pharm, Pusan 609735, South Korea
[3] Pusan Natl Univ, Coll Home Econ, Dept Clothing & Text, Pusan 609735, South Korea
关键词
Curcuma longa L; diarylheptanoids; peroxynitrite; zingiberaceae;
D O I
10.1002/ptr.1179
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Peroxynitrite is a cytotoxic intermediate produced by the reaction between the superoxide anion (0,) and nitric oxide (NO). The aim of this study was to investigate the scavenging effects of Curcuma longa L. on authentic peroxynitrite, and further studies are planned that will attempt to identify the active principles from the active fractions. The methanolic extract of C. longa showed 50% scavenging activity (IC50) at concentration of 1.7 +/- 0.08 mug/ml, and was thus fractionated with several solvents. The peroxynitrite scavenging activity potential of the individual fraction was in the order of ethyl acetate > dichloromethane > water fraction. The ethyl acetate soluble fraction exhibiting strong scavenging activity was further purified by repeated silica gel column chromatography. Peroxynitrite scavenging diarytheptanoids, curcumin I (1), curcumin II (2), and curcumin III (3) were isolated as active principles. Compounds 1-3 showed the peroxynitrite scavenging activities with IC50 values of 4.0 +/- 0.04, 6.4 +/- 0.30, and 29.7 +/- 1.29 muM respectively. Penicillamine as positive control exhibited IC50 value of 2.38 +/- 0.34 muM. The structure-activity relationship of diarylheptanoids on peroxynitrite was also discussed. Copyright (C) 2003 John Wiley Sons, Ltd.
引用
收藏
页码:481 / 484
页数:4
相关论文
共 25 条
[1]  
HUANG MT, 1992, ACS SYM SER, V507, P8
[2]   ANTIOXIDANT ACTIVITY OF TROPICAL GINGER EXTRACTS AND ANALYSIS OF THE CONTAINED CURCUMINOIDS [J].
JITOE, A ;
MASUDA, T ;
TENGAH, IGP ;
SUPRAPTA, DN ;
GARA, IW ;
NAKATANI, N .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1992, 40 (08) :1337-1340
[3]   Phenolic antioxidants prevent peroxynitrite-derived collagen modification in vitro [J].
Kato, Y ;
Ogino, Y ;
Aoki, T ;
Uchida, K ;
Kawakishi, S ;
Osawa, T .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1997, 45 (08) :3004-3009
[4]   Inhibition of peroxynitrite-mediated oxidation of dopamine by flavonoid and phenolic antioxidants and their structural relationships [J].
Kerry, N ;
Rice-Evans, C .
JOURNAL OF NEUROCHEMISTRY, 1999, 73 (01) :247-253
[5]  
KIM AR, 2001, UNPUB PHYTOTHERAPY R
[6]   PEROXYNITRITE-MEDIATED OXIDATION OF DIHYDRORHODAMINE-123 [J].
KOOY, NW ;
ROYALL, JA ;
ISCHIROPOULOS, H ;
BECKMAN, JS .
FREE RADICAL BIOLOGY AND MEDICINE, 1994, 16 (02) :149-156
[7]   OXYGEN RADICAL SCAVENGING ACTIVITY OF CURCUMIN [J].
KUNCHANDY, E ;
RAO, MNA .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1990, 58 (03) :237-240
[8]   EFFECT OF CURCUMIN ON HYDROXYL RADICAL GENERATION THROUGH FENTON REACTION [J].
KUNCHANDY, E ;
RAO, MNA .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1989, 57 (02) :173-176
[9]   THE ANTIOXIDANTS OF HIGHER-PLANTS [J].
LARSON, RA .
PHYTOCHEMISTRY, 1988, 27 (04) :969-978
[10]   Chemical studies on antioxidant mechanism of curcuminoid: Analysis of radical reaction products from curcumin [J].
Masuda, T ;
Hidaka, K ;
Shinohara, A ;
Maekawa, T ;
Takeda, Y ;
Yamaguchi, H .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1999, 47 (01) :71-77