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枳苷通过使RAW 264.7巨噬细胞中的核因子κB失活来抑制脂多糖诱导的诱导型一氧化氮合酶、环氧化酶-2和细胞因子的表达。

Inhibition of LPS-induced iNOS, COX-2 and cytokines expression by poncirin through the NF-kappaB inactivation in RAW 264.7 macrophage cells.

作者信息

Kim Jong-Bin, Han Ah-Reum, Park Eun-Young, Kim Ji-Yeon, Cho Woong, Lee Jun, Seo Eun-Kyoung, Lee Kyung-Tae

机构信息

Department of Pharmaceutical Biochemistry, College of Pharmacy, Kyung-Hee University, Dongdaemun-ku, Hoegi- Dong, Seoul 130-701, South Korea.

出版信息

Biol Pharm Bull. 2007 Dec;30(12):2345-51. doi: 10.1248/bpb.30.2345.

DOI:10.1248/bpb.30.2345
PMID:18057724
Abstract

We previously reported that poncirin, a flavanone glycoside isolated from the EtOAc extract of the dried immature fruits of Poncirus trifoliata, is an anti-inflammatory compound that inhibits PGE(2) and IL-6 production. The present work was undertaken to investigate the molecular actions of poncirin in RAW 264.7 macrophage cell line. Poncirin reduced lipopolysaccharide (LPS)-induced protein levels of inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) and the mRNA expressions of iNOS, COX-2, tumor necrosis factor-alpha (TNF-alpha) and interleukin-6 (IL-6) in a concentration-dependent manner, as determined by Western blotting and RT-PCR, respectively. Furthermore, poncirin inhibited the LPS-induced DNA binding activity of nuclear factor-kappaB (NF-kappaB). Moreover, this effect was accompanied by a parallel reduction in IkappaB-alpha degradation and phosphorylation that in by nuclear translocations of p50 and p65 NF-kappaB subunits. Taken together, our data indicate that anti-inflammatory properties of poncirin might be the result from the inhibition iNOS, COX-2, TNF-alpha and IL-6 expression via the down-regulation of NF-kappaB binding activity.

摘要

我们之前报道过,从枳壳干燥未成熟果实的乙酸乙酯提取物中分离得到的黄烷酮糖苷柚皮苷是一种抗炎化合物,可抑制前列腺素E2(PGE2)和白细胞介素6(IL-6)的产生。目前的研究旨在探讨柚皮苷在RAW 264.7巨噬细胞系中的分子作用。通过蛋白质印迹法和逆转录-聚合酶链反应(RT-PCR)分别测定,柚皮苷以浓度依赖的方式降低了脂多糖(LPS)诱导的诱导型一氧化氮合酶(iNOS)和环氧化酶-2(COX-2)的蛋白水平以及iNOS、COX-2、肿瘤坏死因子-α(TNF-α)和白细胞介素-6(IL-6)的mRNA表达。此外,柚皮苷抑制了LPS诱导的核因子-κB(NF-κB)的DNA结合活性。而且,这种作用伴随着IκB-α降解和磷酸化的平行降低,以及p50和p65 NF-κB亚基的核转位。综上所述,我们的数据表明,柚皮苷的抗炎特性可能是通过下调NF-κB结合活性来抑制iNOS、COX-2、TNF-α和IL-6表达的结果。

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