Short-Chain Fatty Acids Suppress Lipopolysaccharide-Induced Production of Nitric Oxide and Proinflammatory Cytokines Through Inhibition of NF-κB Pathway in RAW264.7 Cells

被引:202
作者
Liu, Tengfei [1 ]
Li, Jing [1 ]
Liu, Yuxin [1 ,2 ]
Xiao, Nan [1 ]
Suo, Haitao [1 ]
Xie, Kun [1 ]
Yang, Chunliu [1 ]
Wu, Chen [3 ]
机构
[1] Hebei Univ, Coll Pharmaceut Sci, Lab Cell Pharmacol, Baoding 071002, Peoples R China
[2] Hebei Univ, Drug Qual Control Key Lab Hebei Prov, Baoding 071002, Peoples R China
[3] Hebei Univ, Coll Life Sci, Baoding 071002, Peoples R China
关键词
SCFAs; LPS; proinflammatory factors; inducible nitric synthase; NF-kappa B p65; HISTONE DEACETYLASE INHIBITOR; PROSTAGLANDIN E-2; MACROPHAGE; BUTYRATE; PROPIONATE; SECRETION; RELEVANCE; HEALTH;
D O I
10.1007/s10753-012-9484-z
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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-alpha (TNF-alpha) and interleukin (IL-1, IL-6, and IL-10)) and to observe the effect of NaAc on inhibiting lipopolysaccharide (LPS)-induced NF-kappa B 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-alpha, IL-1 beta, 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 mu mol/L). Like NaB, NaAC inhibited LPS-induced NF-kappa B activation. These results may hold promise on the role that SCFAs have on the prevention and treatment of various inflammatory conditions.
引用
收藏
页码:1676 / 1684
页数:9
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