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短链脂肪酸通过抑制 RAW264.7 细胞中的 NF-κB 通路抑制脂多糖诱导的一氧化氮和前炎性细胞因子的产生。

Short-chain fatty acids suppress lipopolysaccharide-induced production of nitric oxide and proinflammatory cytokines through inhibition of NF-κB pathway in RAW264.7 cells.

机构信息

Laboratory of Cell Pharmacology, College of Pharmaceutical Sciences, Hebei University, 180 East Wusi Road, Baoding 071002, China.

出版信息

Inflammation. 2012 Oct;35(5):1676-84. doi: 10.1007/s10753-012-9484-z.

Abstract

Short-chain fatty acids (SCFAs) produced by the colonic bacterial fermentation of dietary fiber contribute a significant proportion of daily energy requirement. Furthermore, these compounds are modulators of macrophage function and potential targets for the development of new drugs. The aims of this study were to evaluate the effects of three types of SCFAs (sodium acetate (NaAc), sodium propionate (NaP), and sodium butyrate (NaB)) on the production of NO and inducible nitric oxide synthase (iNOS) and proinflammatory and antiinflammatory cytokines (tumor necrosis factor-α (TNF-α) and interleukin (IL-1, IL-6, and IL-10)) and to observe the effect of NaAc on inhibiting lipopolysaccharide (LPS)-induced NF-κB activation in LPS-stimulated RAW264.7 cells. The results show that three types of SCFAs (acetate, propionate, and butyrate) reduced the production of proinflammatory factors, including TNF-α, IL-1β, IL-6, and NO, and inhibited the vitality of iNOS. Meanwhile, SCFAs enhanced the production of antiinflammatory cytokine IL-10 in lower concentrations (1-1,200 μmol/L). Like NaB, NaAC inhibited LPS-induced NF-κB activation. These results may hold promise on the role that SCFAs have on the prevention and treatment of various inflammatory conditions.

摘要

短链脂肪酸(SCFAs)是膳食纤维在结肠细菌发酵产生的,它们为每日能量需求贡献了相当大的比例。此外,这些化合物是巨噬细胞功能的调节剂,也是开发新药的潜在靶点。本研究旨在评估三种 SCFAs(乙酸钠(NaAc)、丙酸钠(NaP)和丁酸钠(NaB))对 NO 和诱导型一氧化氮合酶(iNOS)以及促炎和抗炎细胞因子(肿瘤坏死因子-α(TNF-α)和白细胞介素(IL-1、IL-6 和 IL-10)的产生的影响,并观察 NaAc 抑制脂多糖(LPS)刺激的 RAW264.7 细胞中 LPS 诱导的 NF-κB 激活的作用。结果表明,三种 SCFAs(乙酸盐、丙酸盐和丁酸盐)均降低了促炎因子(包括 TNF-α、IL-1β、IL-6 和 NO)的产生,并抑制了 iNOS 的活力。同时,SCFAs 在较低浓度(1-1,200μmol/L)下增强了抗炎细胞因子 IL-10 的产生。与 NaB 一样,NaAC 抑制了 LPS 诱导的 NF-κB 激活。这些结果可能对 SCFAs 在预防和治疗各种炎症状态方面的作用具有重要意义。

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