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相思树木心的植物化合物对炎症介质产生的影响。

Effect of phytocompounds from the heartwood of Acacia confusa on inflammatory mediator production.

作者信息

Wu Jyh-Horng, Tung Yu-Tang, Chien Shih-Chang, Wang Sheng-Yang, Kuo Yueh-Hsiung, Shyur Lie-Fen, Chang Shang-Tzen

机构信息

Department of Forestry, National Chung-Hsing University, Taichung 402, Taiwan.

出版信息

J Agric Food Chem. 2008 Mar 12;56(5):1567-73. doi: 10.1021/jf072922s. Epub 2008 Feb 7.

DOI:10.1021/jf072922s
PMID:18254591
Abstract

Acacia confusa Merr. (Leguminosae) is traditionally used as a medicinal plant in Taiwan. In the present study, anti-inflammatory activity of extracts from the heartwood of A. confusa were investigated for the first time. Results demonstrated that ethanolic extracts of A. confusa heartwood strongly suppressed NO production in lipopolysaccharide (LPS)-activated RAW 264.7 macrophages. Among all fractions derived from ethanolic extracts, the EtOAc fraction exhibited the best inhibitory activity. Following column chromatography and reverse-phase high-performance liquid chromatography, 13 specific phytocompounds including 5 new flavonoids (i.e., 7,8,3',4'-tetrahydroxy-4-methoxyflavan-3-ol, 7,8,3',4'-tetrahydroxyflavone, 7,8,3'-trihydroxy-3,4'-dimethoxyflavone, 7,3',4'-trihydroxyflavone, and 7,3',4'-trihydroxy-3-methoxyflavone) were isolated and identified from the EtOAc fraction. In addition, melanoxetin (3,7,8,3',4'-pentahydroxyflavone), a major compound in the EtOAc fraction, markedly suppressed LPS-induced NO and prostaglandin E 2 (PGE 2) production. Moreover, melanoxetin completely suppressed gene expression of inducible NO synthase (iNOS) and cyclooxygenase-2 (COX-2) at 50 and 100 microM, respectively. This is the first report to identify the inhibitory bioactivities of melanoxetin on iNOS and COX-2.

摘要

相思树(含羞草科)在台湾传统上被用作药用植物。在本研究中,首次对相思树木心提取物的抗炎活性进行了研究。结果表明,相思树木心的乙醇提取物强烈抑制脂多糖(LPS)激活的RAW 264.7巨噬细胞中一氧化氮(NO)的产生。在乙醇提取物的所有馏分中,乙酸乙酯馏分表现出最佳的抑制活性。经过柱色谱和反相高效液相色谱分离,从乙酸乙酯馏分中分离并鉴定出13种特定的植物化合物,包括5种新的黄酮类化合物(即7,8,3',4'-四羟基-4-甲氧基黄烷-3-醇、7,8,3',4'-四羟基黄酮、7,8,3'-三羟基-3,4'-二甲氧基黄酮、7,3',4'-三羟基黄酮和7,3',4'-三羟基-3-甲氧基黄酮)。此外,乙酸乙酯馏分中的主要化合物黑素素(3,7,8,3',4'-五羟基黄酮)显著抑制LPS诱导的NO和前列腺素E2(PGE2)的产生。此外,黑素素在50和100 microM时分别完全抑制诱导型一氧化氮合酶(iNOS)和环氧化酶-2(COX-2)的基因表达。这是首次报道黑素素对iNOS和COX-2的抑制生物活性。

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