Maiuri Maria Chiara, De Stefano Daniela, Di Meglio Paola, Irace Carlo, Savarese Maria, Sacchi Raffaele, Cinelli Maria Pia, Carnuccio Rosa
Dipartimento di Farmacologia Sperimentale, Università degli Studi di Napoli Federico II, Via D. Montesano n. 49, 80131 Naples, Italy.
Naunyn Schmiedebergs Arch Pharmacol. 2005 Jun;371(6):457-65. doi: 10.1007/s00210-005-1078-y. Epub 2005 Jul 16.
We investigated the effect of hydroxytyrosol (HT), a phenolic compound from virgin olive oil, on inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) expression in J774 murine macrophages stimulated with lipopolysaccharide (LPS). Incubation of cells with LPS caused an increase in iNOS and COX-2 mRNA and protein level as well as ROS generation, which was prevented by HT. In addition, HT blocked the activation of nuclear factor-kappaB (NF-kappaB), signal transducer and activator of transcription-1alpha (STAT-1alpha) and interferon regulatory factor-1 (IRF-1). These results, showing that HT down-regulates iNOS and COX-2 gene expression by preventing NF-kappaB, STAT-1alpha and IRF-1 activation mediated through LPS-induced ROS generation, suggest that it may represent a non-toxic agent for the control of pro-inflammatory genes.
我们研究了来自初榨橄榄油的酚类化合物羟基酪醇(HT)对脂多糖(LPS)刺激的J774鼠巨噬细胞中诱导型一氧化氮合酶(iNOS)和环氧化酶-2(COX-2)表达的影响。用LPS孵育细胞导致iNOS和COX-2 mRNA及蛋白水平增加以及活性氧(ROS)生成,而HT可阻止这种情况。此外,HT阻断了核因子-κB(NF-κB)、信号转导和转录激活因子-1α(STAT-1α)以及干扰素调节因子-1(IRF-1)的激活。这些结果表明,HT通过阻止由LPS诱导的ROS生成介导的NF-κB、STAT-1α和IRF-1激活来下调iNOS和COX-2基因表达,提示它可能是一种用于控制促炎基因的无毒剂。