PMID- 26400435 OWN - NLM STAT- MEDLINE DCOM- 20160706 LR - 20181113 IS - 1541-1087 (Electronic) IS - 0731-5724 (Print) IS - 0731-5724 (Linking) VI - 34 Suppl 1 IP - 0 1 DP - 2015 TI - Mitigation of Inflammation-Induced Mood Dysregulation by Long-Chain Omega-3 Fatty Acids. PG - 48-55 LID - 10.1080/07315724.2015.1080527 [doi] AB - Although evidence suggests that chronic elevations in immune-inflammatory signaling can precipitate mood symptoms in a subset of individuals, associated risk and resilience mechanisms remain poorly understood. Long-chain omega-3 (LCn-3) fatty acids, including eicosapentaenic acid (EPA) and docosahexaenoic acid (DHA), have anti-inflammatory and inflammation-resolving properties that maintain immune-inflammatory signaling homeostasis. Cross-sectional evidence suggests that the mood disorders major depressive disorder and bipolar disorder are associated with low EPA and/or DHA biostatus, elevations in the LCn-6:LCn-3 fatty acid ratio, and elevated levels of pro-inflammatory eicosanoids, cytokines, and acute-phase proteins. Medications that are effective for reducing depressive symptoms or stabilizing manic depressive oscillations may act in part by downregulating immune-inflammatory signaling and are augmented by anti-inflammatory medications. Recent prospective longitudinal evidence suggests that elevations in the LCn-6:LCn-3 fatty acid ratio are a modifiable risk factor for the development of mood symptoms, including depression and irritability, in response to immune-inflammatory signaling. Together these data suggest that increasing LCn-3 fatty acid intake and biostatus represents a feasible strategy to mitigate the negative impact of elevated immune-inflammatory signaling on mood stability. Key teaching points: * Long-chain omega-3 (LCn-3) fatty acids have anti-inflammatory and inflammation-resolving properties. * Major mood disorders are associated with both LCn-3 fatty acids deficiency and elevated immune-inflammatory signaling. * Prospective evidence suggests that low LCn-3 fatty acid biostatus increases risk for developing inflammation-induced mood dysregulation. * Taken collectively, this evidence suggests that increasing LCn-3 fatty acid intake and biostatus represents a promising strategy to mitigate the detrimental effects of elevated immune-inflammatory signaling on mood. FAU - McNamara, Robert K AU - McNamara RK AD - a Department of Psychiatry and Behavioral Neuroscience , Division of Bipolar Disorders Research, University of Cincinnati College of Medicine , Cincinnati , Ohio. LA - eng GR - R01 DK097599/DK/NIDDK NIH HHS/United States GR - DK097599/DK/NIDDK NIH HHS/United States PT - Journal Article PT - Research Support, N.I.H., Extramural PL - United States TA - J Am Coll Nutr JT - Journal of the American College of Nutrition JID - 8215879 RN - 0 (Acute-Phase Proteins) RN - 0 (Anti-Inflammatory Agents) RN - 0 (Cytokines) RN - 25167-62-8 (Docosahexaenoic Acids) RN - AAN7QOV9EA (Eicosapentaenoic Acid) SB - IM MH - Acute-Phase Proteins/metabolism MH - Affect MH - Anti-Inflammatory Agents/*pharmacology MH - Cross-Sectional Studies MH - Cytokines/metabolism MH - Docosahexaenoic Acids/*pharmacology MH - Eicosapentaenoic Acid/*pharmacology MH - Humans MH - Inflammation/*complications/immunology MH - Mood Disorders/*drug therapy/etiology/immunology MH - Prospective Studies MH - Risk Factors MH - Signal Transduction/drug effects PMC - PMC4686371 MID - NIHMS744732 OTO - NOTNLM OT - arachidonic acid OT - bipolar disorder OT - cytokines OT - depression OT - docosahexaenoic acid (DHA) OT - inflammation OT - mood OT - omega-3 fatty acids EDAT- 2015/09/25 06:00 MHDA- 2016/07/07 06:00 PMCR- 2016/01/01 CRDT- 2015/09/25 06:00 PHST- 2015/09/25 06:00 [entrez] PHST- 2015/09/25 06:00 [pubmed] PHST- 2016/07/07 06:00 [medline] PHST- 2016/01/01 00:00 [pmc-release] AID - 10.1080/07315724.2015.1080527 [doi] PST - ppublish SO - J Am Coll Nutr. 2015;34 Suppl 1(0 1):48-55. doi: 10.1080/07315724.2015.1080527.