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草果通过Nrf2依赖的血红素加氧酶-1表达抑制脂多糖诱导的RAW264.7巨噬细胞炎症反应。

Amomum tsao-ko suppresses lipopolysaccharide-induced inflammatory responses in RAW264.7 macrophages via Nrf2-dependent heme oxygenase-1 expression.

作者信息

Li Bin, Choi Hee-Jin, Lee Dong-Sung, Oh Hyuncheol, Kim Youn-Chul, Moon Jin-Young, Park Won-Hwan, Park Sun-Dong, Kim Jai-Eun

机构信息

Department of Pharmacy, Qingdao University of Science & Technology, Qingdao 266042, P. R. China.

出版信息

Am J Chin Med. 2014;42(5):1229-44. doi: 10.1142/S0192415X14500773. Epub 2014 Sep 1.

Abstract

Amomum tsao-ko Crevost et Lemaire, used as a spice in Asia, is an important source of Chinese cuisine and traditional Chinese medicines. A. tsao-ko is reported to exert a variety of biological and pharmacological activities, including anti-proliferative, anti-oxidative and neuroprotective effects. In this study, NNMBS227, consisting of the ethanol extract of A. tsao-ko, exhibited potent anti-inflammatory activities in RAW264.7 macrophages. We investigated the effect of NNMBS227 in the suppression of pro-inflammatory mediators, including pro-inflammatory enzymes (inducible nitric oxide synthase and cyclooxygenase-2) and cytokines (tumor necrosis factor-α and interleukin-1β) in LPS stimulated macrophages. NNMBS227 also inhibited the phosphorylation and degradation of IκB-α, as well as the nuclear translocation of nuclear factor kappa B (NF-κB) p65 caused by stimulation with LPS. In addition, NNMBS227 induced heme oxygenase (HO)-1 expression through the nuclear translocation of nuclear factor E2-related factor 2 (Nrf2) in macrophages. Using tin protoporphyrin (SnPP), an HO activity inhibitor, we confirmed an association between the anti-inflammatory effects of NNMBS227 and the up-regulation of HO-1. These findings suggest that Nrf2-dependent increases in the expression of HO-1 induced by NNMBS227 conferred anti-inflammatory activities in LPS stimulated RAW264.7 macrophages.

摘要

草果是一种在亚洲用作香料的植物,是中国菜肴和传统中药的重要来源。据报道,草果具有多种生物和药理活性,包括抗增殖、抗氧化和神经保护作用。在本研究中,由草果乙醇提取物组成的NNMBS227在RAW264.7巨噬细胞中表现出强大的抗炎活性。我们研究了NNMBS227对LPS刺激的巨噬细胞中促炎介质的抑制作用,这些促炎介质包括促炎酶(诱导型一氧化氮合酶和环氧化酶-2)和细胞因子(肿瘤坏死因子-α和白细胞介素-1β)。NNMBS227还抑制了IκB-α的磷酸化和降解,以及LPS刺激引起的核因子κB(NF-κB)p65的核转位。此外,NNMBS227通过巨噬细胞中核因子E2相关因子2(Nrf2)的核转位诱导血红素加氧酶(HO)-1表达。使用HO活性抑制剂锡原卟啉(SnPP),我们证实了NNMBS227的抗炎作用与HO-1的上调之间存在关联。这些发现表明,NNMBS227诱导的Nrf2依赖性HO-1表达增加赋予了LPS刺激的RAW264.7巨噬细胞抗炎活性。

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