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Omega-3 Fatty Acids Prevent Inflammation and Metabolic Disorder through Inhibition of NLRP3 Inflammasome Activation

机译:Omega-3脂肪酸通过抑制NLRP3炎症小体活化来预防炎症和代谢紊乱

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摘要

Omega-3 fatty acids (ω-3 FAs) have potential anti-inflammatory activity in a variety of inflammatory human diseases, but the mechanisms remain poorlyunderstood. Here we show that stimulation of macrophages with ω-3 FAs, including eicosapentaenoic acid (EPA), docosahexaenoic acid (DHA), and other family members, abolished NLRP3 inflammasome activation and inhibited subsequent caspase-1 activation and IL-1β secretion. In addition, G protein-coupled receptor 120 (GPR120) andGPR40 and their downstream scaffold protein β-arrestin-2 were shown to be involved in inflammasome inhibition induced by ω-3 FAs. Importantly, ω-3FAs also prevented NLRP3 inflammasome-dependent inflammation and metabolic disorder in a high-fat-diet-induced type 2 diabetes model. Ourresults reveal a mechanism through which ω-3 FAs repress inflammation and prevent inflammation-driven diseases and suggest the potential clinical use of ω-3 FAs in gout, autoinflammatory syndromes, or other NLRP3 inflammasome-driven inflammatory diseases.
机译:Omega-3脂肪酸(ω-3FAs)在多种人类炎性疾病中均具有潜在的抗炎活性,但其机理尚不清楚。在这里,我们发现用ω-3FAs刺激巨噬细胞,包括二十碳五烯酸(EPA),二十二碳六烯酸(DHA)和其他家族成员,废除了NLRP3炎症小体激活并抑制了随后的caspase-1激活和IL-1β分泌。此外,G蛋白偶联受体120(GPR120)和GPR40及其下游支架蛋白β-arrestin-2被证明与ω-3FAs诱导的炎性体抑制有关。重要的是,在高脂饮食诱导的2型糖尿病模型中,ω-3FAs还可以预防NLRP3炎性体依赖性炎症和代谢紊乱。我们的结果揭示了ω-3FA抑制炎症并预防炎症驱动疾病的机制,并暗示了ω-3FA在痛风,自体炎症综合征或其他NLRP3炎症小体驱动的炎症疾病中的潜在临床应用。

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