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Bioenergetic characterization of macrophage inflammatory responses attenuated by anthocyanins (383.2)
Author(s) -
Komarnytsky Slavko,
Chen Amelia,
Thor Yiwen,
Palatini Kimberly,
Wilson Mickey,
Esposito Debora
Publication year - 2014
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fasebj.28.1_supplement.383.2
Subject(s) - bioenergetics , chemistry , glycolysis , inflammation , oxidative phosphorylation , biochemistry , extracellular , delphinidin , pharmacology , metabolism , mitochondrion , biology , immunology , antioxidant , cyanidin
Anthocyanins present strong anti‐inflammatory properties, thus leading to the potential use as functional food ingredients for the prevention and treatment of chronic inflammatory diseases and increased intestinal permeability to endotoxins, notably LPS. However, the differences between individual anthocyanins and their effects on cellular signaling and metabolism need to be further elucidated. In this study, we evaluated the protection afforded by anthocyanins against LPS‐induced inflammatory response in RAW 264.7 macrophages and determined changes in oxygen consumption rates (OCR) and extracellular acidification rates (ECAR) during the macrophage activation. Basal OCR and ECAR increased as the macrophages underwent LPS stimulation from 283.3±38.4 to 361.7±47.9 pmol/min, and from 9.7±2.4 to 27.6±3.8 mpH/min, respectively, suggesting that energy required for activation is rapidly provided by changes in glycolytic pathways. When tested in physiological concentrations (0.1‐3 uM), malvidin and, to a certain degree, delphinidin, were more effective than cyaniding or pelargonidin in the reduction of mRNA and protein biomarkers of inflammation. Different effects exerted by individual anthocyanins suggested that the presence of the methylated hydroxyls on the B ring may be critical for their greater biological activity. Anthocyanin‐treated macrophages developed a distinct metabolic profile with respect to glycolysis versus oxidative phosphorylation, in part by increasing spare respiratory capacity and therefore shifting to mitochondria as their main source of ATP. Grant Funding Source : Supported by NCSU faculty start up funds to SK.