Inflammatory signaling and metabolic regulation by nitro-fatty acids
The addition of nitrogen dioxide (NO2) to the double bond of unsaturated fatty acids yields an array of electrophilic nitro-fatty acids (NO2-FA) with unique biochemical and signaling properties. During the last decade, NO2-FA have been shown to exert a protective role in various inflammatory and met...
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Published in | Nitric oxide Vol. 78; pp. 140 - 145 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
01.08.2018
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Subjects | |
Online Access | Get full text |
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Summary: | The addition of nitrogen dioxide (NO2) to the double bond of unsaturated fatty acids yields an array of electrophilic nitro-fatty acids (NO2-FA) with unique biochemical and signaling properties. During the last decade, NO2-FA have been shown to exert a protective role in various inflammatory and metabolic disorders. NO2-FA exert their biological effects primarily by regulating two central physiological adaptive responses: the canonical inflammatory signaling and metabolic pathways. In this mini-review, we summarize current knowledge on the regulatory role of NO2-FA in the inflammatory and metabolic response via regulation of nuclear factor kappa B (NF-κB) and peroxisome proliferator-activated receptor γ (PPARγ), master regulators of inflammation and metabolism. Moreover, the engagement of novel signaling and metabolic pathways influenced by NO2-FA, beyond NF-κB and PPAR signaling, is discussed herein.
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•NO2-FA modulate key signaling pathways via posttranslational modifications.•NO2-FA inhibit NF-κB via direct p65 nitroalkylation and regulate Toll-like receptor signaling.•NO2-FA are PPARγ ligands that differ from thiazolidinediones in receptor affinity and extent of activation.•This mini-review conveys the protective role of NO2-FA in inflammatory responses and regulation of metabolic pathways.•Content. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-3 content type line 23 ObjectType-Review-1 |
ISSN: | 1089-8603 1089-8611 |
DOI: | 10.1016/j.niox.2018.03.017 |