Article ID Journal Published Year Pages File Type
2019561 Prostaglandins & Other Lipid Mediators 2013 8 Pages PDF
Abstract

•We studied effects of mPGES-1 deletion on eicosanoids and fatty acids in mice.•mPGES-1 deletion increased PGD2 metabolites and 13-HODE in peritoneal macrophages.•mPGES-1 depletion altered the total lipid fatty acid composition in mouse spleen.

mPGES-1 is considered an alternative target for anti-inflammatory treatment with improved selectivity and safety compared to NSAIDs. mPGES-1 depletion not only suppresses inflammation via absence of inducible PGE2 but might also cause an activation of anti-inflammatory pathways. We studied effects of mPGES-1 deletion on the eicosanoid and fatty acid (FA) profiles in mice. In LPS-induced peritoneal macrophages from mPGES-1 knock-out (mPGES-1−/−, KO) mice PGE2 production was markedly attenuated, whereas levels of PGD2 metabolites (15-deoxy-Δ12,14 PGJ2 and 15-deoxy-Δ12,14 PGD2) were increased compared to wild type mice. The levels of oxidized fatty acid 13-HODE were also significantly up-regulated in KO macrophages. Significant differences in the total lipid FA composition (decrease in monounsaturated FA and increase in eicosadienoic acid) were detected in spleen of KO and WT mice. These effects of mPGES-1 deletion on eicosanoid and fatty acid metabolism have important implications for future mPGES-1 inhibitors and deserve further investigation.

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