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原花青素B-4 3'-O-没食子酸酯,一种茶多酚,通过下调TAK1-NF-κB通路参与对COX-2和iNOS的抑制。

Prodelphinidin B-4 3'-O-gallate, a tea polyphenol, is involved in the inhibition of COX-2 and iNOS via the downregulation of TAK1-NF-kappaB pathway.

作者信息

Hou De-Xing, Luo Dong, Tanigawa Shunsuke, Hashimoto Fumio, Uto Takuhiro, Masuzaki Satoko, Fujii Makoto, Sakata Yusuke

机构信息

Department of Biochemical Science and Technology, Faculty of Agriculture, Kagoshima University, Korimoto 1-21-24, Kagoshima City 890-0065, Japan.

出版信息

Biochem Pharmacol. 2007 Sep 1;74(5):742-51. doi: 10.1016/j.bcp.2007.06.006. Epub 2007 Jun 14.

Abstract

Much is known about the bioactive properties of green tea flavan-3-ol. However, very little work has been done to determine the properties of proanthocyanidins, another kind of polyphenols in green tea. In this study, we have investigated the anti-inflammatory effect of tea prodelphinidin B-4 3'-O-gallate (PDG) by demonstrating the inhibitory effects on cyclooxygenase-2 (COX-2) and inducible nitric oxide synthase (iNOS) in lipopolysaccharide (LPS)-activated murine macrophage RAW264 cells. PDG caused a dose-dependent inhibition of COX-2 and iNOS at both mRNA and protein levels with the attendant decrease of prostaglandin E2 (PGE2) and nitric oxide (NO) production. Molecular data revealed that PDG downregulated NF-kappaB signaling pathway. Electrophoretic mobility shift assay (EMSA) showed that PDG reduced the binding complex of NF-kappaB-DNA in the promoter of COX-2 and iNOS. Immunochemical analysis revealed that PDG suppressed LPS-induced phosphorylation and degradation of IkappaBalpha, and subsequent nuclear translocation of p65. Consequently, PDG suppressed phosphorylation of IkappaB kinase alpha/beta (IKKalpha/beta) and TGF-beta-activated kinase (TAK1). Taken together, our data indicated that PDG is involved in the inhibition of COX-2 and iNOS via the downregulation of TAK1-NF-kappaB pathway, revealing partial molecular basis for the anti-inflammatory properties of tea PDG.

摘要

关于绿茶黄烷-3-醇的生物活性特性,人们已经了解很多。然而,对于绿茶中另一种多酚类物质原花青素的特性,却很少有研究。在本研究中,我们通过证明茶原花青素B-4 3'-O-没食子酸酯(PDG)对脂多糖(LPS)激活的小鼠巨噬细胞RAW264细胞中环氧化酶-2(COX-2)和诱导型一氧化氮合酶(iNOS)的抑制作用,来研究其抗炎作用。PDG在mRNA和蛋白质水平上均导致COX-2和iNOS的剂量依赖性抑制,同时伴随着前列腺素E2(PGE2)和一氧化氮(NO)生成的减少。分子数据显示,PDG下调了NF-κB信号通路。电泳迁移率变动分析(EMSA)表明,PDG减少了COX-2和iNOS启动子中NF-κB-DNA的结合复合物。免疫化学分析显示,PDG抑制了LPS诱导的IκBα的磷酸化和降解,以及随后p65的核转位。因此,PDG抑制了IκB激酶α/β(IKKα/β)和TGF-β激活激酶(TAK1)的磷酸化。综上所述,我们的数据表明,PDG通过下调TAK1-NF-κB途径参与了对COX-2和iNOS的抑制,揭示了茶PDG抗炎特性的部分分子基础。

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