闭鞘姜中查耳酮类似物小豆蔻明对核因子-κB信号通路的阻断及抗炎活性

Blockade of nuclear factor-kappaB signaling pathway and anti-inflammatory activity of cardamomin, a chalcone analog from Alpinia conchigera.

作者信息

Lee Jeong-Hyung, Jung Haeng Sun, Giang Phan Minh, Jin Xuejun, Lee Sangku, Son Phan Tong, Lee Dongho, Hong Young-Soo, Lee Kyeong, Lee Jung Joon

机构信息

Anticancer Research Laboratory, Korea Research Institute of Bioscience and Biotechnology, P.O. Box 115, Yuseong, Daejeon 305-600, Korea.

出版信息

J Pharmacol Exp Ther. 2006 Jan;316(1):271-8. doi: 10.1124/jpet.105.092486. Epub 2005 Sep 23.

Abstract

Nuclear factor-kappaB (NF-kappaB) and the signaling pathways that regulate its activity have become a focal point for intense drug discovery and development efforts. NF-kappaB regulates the transcription of a large number of genes, particularly those involved in immune, inflammatory, and antiapoptotic responses. In our search for NF-kappaB inhibitors from natural resources, we identified cardamomin, 2',4'-dihydroxy-6'-methoxychalcone, as an inhibitor of NF-kappaB activation from Alpinia conchigera Griff (Zingiberaceae). In present study, we demonstrated the effect of cardamomin on NF-kappaB activation in lipopolysaccharide (LPS)-stimulated RAW264.7 cells and LPS-induced mortality. This compound significantly inhibited the induced expression of NF-kappaB reporter gene by LPS or tumor necrosis factor (TNF)-alpha in a dose-dependent manner. LPS-induced production of TNF-alpha and NO as well as expression of inducible nitric-oxide synthase and cyclooxygenase-2 was significantly suppressed by the treatment of cardamomin in RAW264.7 cells. Also, cardamomin inhibited not only LPS-induced degradation and phosphorylation of inhibitor kappaBalpha (IkappaBalpha) but also activation of inhibitor kappaB (IkappaB) kinases and nuclear translocation of NF-kappaB. Further analyses revealed that cardamomin did not directly inhibit IkappaB kinases, but it significantly suppressed LPS-induced activation of Akt. Moreover, cardamomin suppressed transcriptional activity and phosphorylation of Ser536 of RelA/p65 subunit of NF-kappaB. However, this compound did not inhibit LPS-induced activation of extracellular signal-regulated kinase and stress-activated protein kinase/c-Jun NH(2)-terminal kinase, but significantly impaired activation of p38 mitogen-activated protein kinase. We also demonstrated that pretreatment of cardamomin rescued C57BL/6 mice from LPS-induced mortality in conjunction with decreased serum level of TNF-alpha. Together, cardamomin could be valuable candidate for the intervention of NF-kappaB-dependent pathological condition such as inflammation.

摘要

核因子-κB(NF-κB)及其调控活性的信号通路已成为药物研发的重点。NF-κB调控大量基因的转录,尤其是那些参与免疫、炎症和抗凋亡反应的基因。在从自然资源中寻找NF-κB抑制剂的过程中,我们从益智(姜科)中鉴定出小豆蔻明,即2',4'-二羟基-6'-甲氧基查耳酮,它是一种NF-κB激活抑制剂。在本研究中,我们证明了小豆蔻明对脂多糖(LPS)刺激的RAW264.7细胞中NF-κB激活及LPS诱导的死亡率的影响。该化合物以剂量依赖的方式显著抑制LPS或肿瘤坏死因子(TNF)-α诱导的NF-κB报告基因的表达。在RAW264.7细胞中,小豆蔻明处理显著抑制了LPS诱导的TNF-α和NO的产生以及诱导型一氧化氮合酶和环氧化酶-2的表达。此外,小豆蔻明不仅抑制LPS诱导的抑制蛋白κBα(IkappaBα)的降解和磷酸化,还抑制抑制蛋白κB(IkappaB)激酶的激活以及NF-κB的核转位。进一步分析表明,小豆蔻明并不直接抑制IkappaB激酶,但它显著抑制LPS诱导的Akt激活。此外,小豆蔻明抑制NF-κB的RelA/p65亚基的转录活性和Ser536的磷酸化。然而,该化合物并不抑制LPS诱导的细胞外信号调节激酶和应激激活蛋白激酶/c-Jun氨基末端激酶的激活,但显著削弱p38丝裂原活化蛋白激酶的激活。我们还证明,小豆蔻明预处理可使C57BL/6小鼠免于LPS诱导的死亡,同时降低血清TNF-α水平。综上所述,小豆蔻明可能是干预NF-κB依赖性病理状况(如炎症)的有价值候选物。

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