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半乳糖牛磺酸钠盐对 LPS 激活的 RAW264.7 细胞的抗炎作用。

Anti-inflammatory Effects of Galactose-Taurine Sodium Salt in LPS-Activated RAW 264.7 Cells.

机构信息

Department of Marine Bio-Food Sciences, Chonnam National University, Yeosu, Republic of Korea.

Department of Food and Nutrition, Inha University, Incheon, Republic of Korea.

出版信息

Adv Exp Med Biol. 2017;975 Pt 2:943-953. doi: 10.1007/978-94-024-1079-2_75.

Abstract

In this study, we synthesized Galactose-Taurine sodium salt (G-T) as a functional food ingredient to enhance biological activities of taurine. Also, anti-inflammatory effects of G-T were investigated in lipopolysaccharide (LPS)-stimulated RAW 264.7 cells. G-T found to reduce the generations of the LPS-stimulated nitric oxide (NO) and prostaglandin E2 (PGE) via down-regulating the expression levels of inducible NO synthase (iNOS) and cyclooxygenase-2 (COX-2). Also, G-T reduced the secretion of inflammatory cytokines including interleukin (IL)-1β, IL-6 and tumor necrosis factor (TNF-α) in LPS-treated RAW 264.7 cells. Finally, we identified that G-T inhibits the activation of nuclear factor-κB (NF-κB) and the phosphorylation of inhibitor κB (IκB)-α. From these results, this study first suggests that G-T could be considered as an effective anti-inflammatory agent.

摘要

在这项研究中,我们合成了半乳糖胺牛磺酸钠盐(G-T)作为一种功能性食品成分,以增强牛磺酸的生物活性。此外,还研究了 G-T 在脂多糖(LPS)刺激的 RAW 264.7 细胞中的抗炎作用。结果发现,G-T 通过下调诱导型一氧化氮合酶(iNOS)和环氧化酶-2(COX-2)的表达水平,减少了 LPS 刺激产生的一氧化氮(NO)和前列腺素 E2(PGE)的产生。此外,G-T 还减少了 LPS 处理的 RAW 264.7 细胞中包括白细胞介素(IL)-1β、IL-6 和肿瘤坏死因子(TNF-α)在内的炎症细胞因子的分泌。最后,我们确定 G-T 抑制了核因子-κB(NF-κB)的激活和抑制κB(IκB)-α的磷酸化。从这些结果来看,本研究首次表明 G-T 可以被视为一种有效的抗炎剂。

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