Literature DB >> 12748983

In vitro peroxynitrite scavenging activity of diarylheptanoids from Curcuma longa.

Jung Eun Kim1, Ae Ra Kim, Hae Young Chung, Shin Young Han, Byung Soo Kim, Jae Sue Choi.   

Abstract

Peroxynitrite is a cytotoxic intermediate produced by the reaction between the superoxide anion (O(2)) 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 (IC(50)) at concentration of 1.7 +/- 0.08 micro g/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 diarylheptanoids, curcumin I (1), curcumin II (2), and curcumin III (3) were isolated as active principles. Compounds 1-3 showed the peroxynitrite scavenging activities with IC(50) values of 4.0 +/- 0.04, 6.4 +/- 0.30, and 29.7 +/- 1.29 micro M, respectively. Penicillamine as positive control exhibited IC(50) value of 2.38 +/- 0.34 micro M. The structure-activity relationship of diarylheptanoids on peroxynitrite was also discussed. Copyright 2003 John Wiley & Sons, Ltd.

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Year:  2003        PMID: 12748983     DOI: 10.1002/ptr.1179

Source DB:  PubMed          Journal:  Phytother Res        ISSN: 0951-418X            Impact factor:   5.878


  13 in total

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