Department of Marine Life Science, Jeju National University, Jeju, Republic of Korea.
Department of Marine Bio-Food Sciences, Chonnam National University, Yeosu, Republic of Korea.
Adv Exp Med Biol. 2017;975 Pt 1:633-642. doi: 10.1007/978-94-024-1079-2_49.
Here, the anti-inflammatory effect of Xylose-Taurine reduced (X-T-R), a taurine derivate was investigated in lipopolysaccharide (LPS)-stimulated RAW 264.7 cells. X-T-R reduced the generations of nitric oxide (NO) and prostaglandin E (PGE) induced by the stimulation of LPS in RAW 264.7 by suppressing the protein expression of iNOS and COX-2 known as inflammatory mediators. Also, X-R-T reduced the expression levels of the pro-inflammatory cytokines such as interleukin (IL)-1β, IL-6 and tumor necrosis factor (TNF-α). Moreover, X-T-R inhibited the activation of nuclear factor-κB (NF-κB) and the phosphorylation of inhibitor κB (IκB)-α. In conclusion, these results first indicate that X-T-R inhibits LPS-induced inflammation by regulating the NF-κB signal pathway in macrophages.
在这里,研究了牛磺酸衍生物 Xylose-Taurine(X-T-R)对脂多糖(LPS)刺激的 RAW 264.7 细胞的抗炎作用。X-T-R 通过抑制已知的炎症介质 iNOS 和 COX-2 的蛋白表达,降低了 LPS 刺激诱导的一氧化氮(NO)和前列腺素 E(PGE)的产生。此外,X-T-R 还降低了促炎细胞因子,如白细胞介素(IL)-1β、IL-6 和肿瘤坏死因子(TNF-α)的表达水平。此外,X-T-R 抑制了核因子-κB(NF-κB)的激活和抑制κB(IκB)-α的磷酸化。总之,这些结果首次表明,X-T-R 通过调节巨噬细胞中的 NF-κB 信号通路抑制 LPS 诱导的炎症。