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Palmitoleic acid reduces the inflammation in LPS ‐stimulated macrophages by inhibition of NF κB, independently of PPAR s
Author(s) -
Souza Camila O,
Teixeira Alexandre AS,
Biondo Luana A,
Silveira Loreana S,
Calder Philip C,
Rosa Neto José C
Publication year - 2017
Publication title -
clinical and experimental pharmacology and physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.752
H-Index - 103
eISSN - 1440-1681
pISSN - 0305-1870
DOI - 10.1111/1440-1681.12736
Subject(s) - inflammation , tlr4 , chemistry , lipopolysaccharide , tumor necrosis factor alpha , inflammasome , macrophage , peroxisome proliferator activated receptor , nf κb , stimulation , microbiology and biotechnology , immunology , endocrinology , biology , receptor , biochemistry , in vitro
Summary Palmitoleic acid ( PM , 16:1n‐7) has anti‐inflammatory properties that could be linked to higher expression of PPAR α, an inhibitor of NF κB. Macrophages play a major role in the pathogenesis of chronic inflammation, however, the effects of PM on macrophages are underexplored. Thus, we aimed to investigate the effects of PM in activated macrophages as well the role of PPAR α. Primary macrophages were isolated from C57 BL /6 wild type ( WT ) and PPAR α knockout ( KO ) mice, cultured under standard conditions and exposed to lipopolysaccharides LPS (2.5 μg/ ml ) and PM 600 μmol/L conjugated with albumin for 24 hours. The stimulation with LPS increased the production of interleukin ( IL )‐6 and IL ‐1β while PM decreased the production of IL ‐6 in WT macrophages. In KO macrophages, LPS increased the production of tumour necrosis factor ( TNF )‐α and IL ‐6 and PM decreased the production of TNF α. The expression of inflammatory markers such NF κB and IL 1β were increased by LPS and decreased by PM in both WT and KO macrophages. PM reduced the expression of MyD88 and caspase‐1 in KO macrophages, and the expression of TLR 4 and HIF ‐1α in both WT and KO macrophages, although LPS had no effect. CD 86, an inflammatory macrophage marker, was reduced by PM independently of genotype. PM increased PPAR γ and reduced PPAR β gene expression in macrophages of both genotypes, and increased ACOX ‐1 expression in KO macrophages. In conclusion, PM promotes anti‐inflammatory effects in macrophages exposed to LPS through inhibition of inflammasome pathway, which was independent of PPAR α, PPAR ϒ and AMPK , thus the molecular mechanisms of anti‐inflammatory response caused by PM is still unclear.