Abstract

BackgroundEicosanoids mediate initiation and resolution of inflammation. Our aim was evaluating the effects of training, exercise and docosahexaenoic (DHA) supplementation on plasma eicosanoids levels and peripheral blood mononuclear cells (PBMCs) eicosanoids production.MethodsFifteen male footballers were distributed to placebo and experimental groups. Experimental group consumed DHA-enriched beverage (1.16 g DHA/day) for 8 weeks, placebo group consumed a placebo beverage. Blood samples were taken before and after the nutritional intervention in basal conditions and 2 h after acute exercise.ResultsTraining increased basal Prostaglandin E1 (PGE1) plasma levels and PBMCs cyclooxygenase 2 (COX-2) protein levels in both groups, but COX-1 protein levels only in the experimental group. Acute exercise increased plasma PGE2 and PBMCs active NFκβ levels. Lipopolysaccharide (LPS)-stimulated PBMCs increases eicosanoids production (PGE1, PGE2, RvD1) in both groups and increased LPS-stimulated PBMCs active NFκβ. DHA supplementation increased COX-2 levels but decreased LPS-stimulated PBMCs PGE1 and PGE2 production. Neither DHA supplementation nor acute exercise altered the expression of NFκβ, COX-2, 15-LOX2, 5-LOX, or IL-1β genes in PBMCs.ConclusionsThe increase of PGE1 plasma levels after training promoted systemic anti-inflammatory and vasodilator environment. Exercise and DHA supplementation acted synergistically by increasing plasma PGE2 with anti-inflammatory effects. Exercise primed PBMCs to enhance PGE1, PGE2 and RvD1 production in response to LPS.Trial registrationThe project was registered at ClinicalTrial.gov (NCT02177383).

Highlights

  • Eicosanoids mediate initiation and resolution of inflammation

  • Eicosapentaenoic acid and docosahexaenoic acid (DHA) can compete with arachidonic acid (AA) as a substrate for cyclooxygenase 2 (COX-2) and 5lipoxygenase (5-LOX), reducing the production of inflammatory mediators derived from AA

  • Prostaglandin E1 (PGE1) and prostaglandin E2 (PGE2) are potent vasodilators which account for the increased blood flow in inflamed areas but PGE1 regulates neutrophil function by reducing neutrophil activation [41]

Read more

Summary

Introduction

Eicosanoids mediate initiation and resolution of inflammation. Our aim was evaluating the effects of training, exercise and docosahexaenoic (DHA) supplementation on plasma eicosanoids levels and peripheral blood mononuclear cells (PBMCs) eicosanoids production. Eicosapentaenoic acid and docosahexaenoic acid (DHA) can compete with AA as a substrate for cyclooxygenase 2 (COX-2) and 5lipoxygenase (5-LOX), reducing the production of inflammatory mediators derived from AA This process plays a critical role in the initial inflammatory response [6, 7, 37]. Prostaglandin E1 (PGE1) and prostaglandin E2 (PGE2) are potent vasodilators which account for the increased blood flow in inflamed areas but PGE1 regulates neutrophil function by reducing neutrophil activation [41] Because of these vasodilator and immune properties, PGs are used as treatment for diseases derived from ischemia-reperfusion, such as arterial occlusive disease and venous ulcers [11, 22, 41]

Objectives
Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call