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血红素加氧酶1介导2',4',6'-三(甲氧基甲氧基)查耳酮的抗炎作用。

Heme oxygenase 1 mediates anti-inflammatory effects of 2',4',6'-tris(methoxymethoxy) chalcone.

作者信息

Lee Sung Hee, Seo Geom Seog, Kim Ji Yeong, Jin Xing Yu, Kim Hee-Doo, Sohn Dong Hwan

机构信息

College of Pharmacy, Medicinal Resources Research Institute, Wonkwang University, Iksan, Jeonbuk 570-749, South Korea.

出版信息

Eur J Pharmacol. 2006 Feb 17;532(1-2):178-86. doi: 10.1016/j.ejphar.2006.01.005. Epub 2006 Feb 14.

Abstract

We report that the synthetic chalcone 2',4',6'-tris(methoxymethoxy) chalcone (TMMC) is an anti-inflammatory compound that reduces nitric oxide (NO) production by inhibiting of inducible NO synthase (iNOS) expression, and that TMMC decreases the degradation of the inhibitory factor kappaB, leading to inhibition of nuclear factor-kappaB translocation into the nucleus in lipopolysaccharide (LPS)-activated RAW 264.7 macrophages. We also demonstrate that TMMC by itself is a potent inducer of heme oxygenase 1 (HO-1). Inhibition of HO-1 activity or scavenging of carbon monoxide, a byproduct of heme degradation, significantly attenuated this anti-inflammatory action. Treating cells with the specific p42/44 MAPK inhibitor, PD98059, blocked the TMMC-mediated induction of HO-1 and the inhibition of LPS-stimulated expression of iNOS. TMMC also depleted intracellular GSH. Our data suggest that TMMC exerts an anti-inflammatory effect in macrophages through a mechanism that involves the induction of HO-1, which is mediated by activation of p42/44 MAPK and GSH depletion.

摘要

我们报告称,合成查耳酮2',4',6'-三(甲氧基甲氧基)查耳酮(TMMC)是一种抗炎化合物,它通过抑制诱导型一氧化氮合酶(iNOS)的表达来减少一氧化氮(NO)的产生,并且TMMC可减少抑制因子κB的降解,从而导致在脂多糖(LPS)激活的RAW 264.7巨噬细胞中抑制核因子κB向细胞核的转位。我们还证明TMMC本身是血红素加氧酶1(HO-1)的有效诱导剂。抑制HO-1活性或清除血红素降解的副产物一氧化碳可显著减弱这种抗炎作用。用特异性p42/44丝裂原活化蛋白激酶(MAPK)抑制剂PD98059处理细胞,可阻断TMMC介导的HO-1诱导以及对LPS刺激的iNOS表达的抑制。TMMC还消耗细胞内谷胱甘肽(GSH)。我们的数据表明,TMMC通过一种涉及诱导HO-1的机制在巨噬细胞中发挥抗炎作用,该机制由p42/44 MAPK的激活和GSH消耗介导。

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