Taechowisan Thongchai, Lu Chunhua, Shen Yuemao, Lumyong Saisamorn
Faculty of Science, Department of Microbiology, Silpakorn University, Nakorn Pathom, Thailand.
Nat Prod Res. 2007 Oct;21(12):1104-13. doi: 10.1080/14786410601129671.
This research was undertaken to find the in vitro inflammatory action of 5,7-dimethoxy-4-p-methoxylphenylcoumarin and 5,7-dimethoxy-4-phenylcoumarin produced by Streptomyces aureofaciens CMUAc130. We investigated the effects of 5,7-dimethoxy-4-p-methoxylphenylcoumarin and 5,7-dimethoxy-4-phenylcoumarin not only on the formation of nitric oxide (NO), PGE(2), TNF-alpha, IL-6 and IL-1beta, but also on inducible NO synthase and cyclooxygenase-2 (COX-2) in lipopolysaccharide (LPS)-induced murine macrophage RAW 264.7 cells. The data obtained were consistent with the modulation of iNOS enzyme expression. A similar fashion was also observed when LPS-induced PGE(2) release and COX-2 expression were tested. The significant inhibitory effects were shown in concentration-dependent manners. In addition, 5,7-dimethoxy-4-p-methoxylphenylcoumarin and 5,7-dimethoxy-4-phenylcoumarin also mildly but significantly reduced the formation of TNF-alpha. These findings support the application of 5,7-dimethoxy-4-p-methoxylphenylcoumarin and 5,7-dimethoxy-4-phenylcoumarin as anti-inflammatory agents.
本研究旨在探究金色链霉菌CMUAc130产生的5,7-二甲氧基-4-对甲氧基苯基香豆素和5,7-二甲氧基-4-苯基香豆素的体外炎症作用。我们研究了5,7-二甲氧基-4-对甲氧基苯基香豆素和5,7-二甲氧基-4-苯基香豆素对脂多糖(LPS)诱导的小鼠巨噬细胞RAW 264.7细胞中一氧化氮(NO)、前列腺素E2(PGE2)、肿瘤坏死因子-α(TNF-α)、白细胞介素-6(IL-6)和白细胞介素-1β(IL-1β)形成的影响,以及对诱导型一氧化氮合酶和环氧合酶-2(COX-2)的影响。获得的数据与诱导型一氧化氮合酶(iNOS)酶表达的调节一致。在测试LPS诱导的PGE2释放和COX-2表达时也观察到类似的情况。显著的抑制作用呈浓度依赖性。此外,5,7-二甲氧基-4-对甲氧基苯基香豆素和5,7-二甲氧基-4-苯基香豆素也轻微但显著地减少了TNF-α的形成。这些发现支持将5,7-二甲氧基-4-对甲氧基苯基香豆素和5,7-二甲氧基-4-苯基香豆素用作抗炎剂。