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Omega-3 fatty acids cause dramatic changes in TLR4 and purinergic eicosanoid signaling

机译:Omega-3脂肪酸导致TLR4和嘌呤能类二十烷酸信号显着变化

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摘要

Dietary fish oil containing ω3 fatty acids, eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), elicit cardioprotective and anti-inflammatory effects through unresolved mechanisms that may involve competition and inhibition at multiple levels. Here, we report the effects of arachidonic acid (AA), EPA, and DHA supplementation on membrane incorporation, phospholipase A_2 catalyzed release, and eicosanoid production in RAW264.7 mac-rophages. Using a targeted lipidomics approach, we observed that Toll-like receptor 4 and purinergic receptor activation of supplemented cells leads to the release of 22-carbon fatty acids that potently inhibit cyclooxygenase pathways. This inhibition was able to shunt metabolism of AA to lipoxygenase pathways, augmenting leukotriene and other lipoxygenase mediator synthesis. In resident peritoneal macrophages, docosapentaenoic acid (DPA) was responsible for cyclooxygenase inhibition after EPA supplementation, offering fresh insights into how EPA exerts anti-inflammatory effects indirectly through elongation to 22-carbon DPA.
机译:含有ω3脂肪酸,二十碳五烯酸(EPA)和二十二碳六烯酸(DHA)的膳食鱼油通过未解决的机制(可能涉及多个竞争和抑制作用)引起心脏保护和抗炎作用。在这里,我们报告花生四烯酸(AA),EPA和DHA补充对RAW264.7巨噬细胞中膜掺入,磷脂酶A_2催化释放和类花生酸产生的影响。使用靶向脂质组学方法,我们观察到Toll样受体4和嘌呤能受体对补充细胞的激活导致释放22-碳脂肪酸,从而有效抑制环氧合酶途径。这种抑制作用能够使AA的代谢分流到脂氧合酶途径,从而增强白三烯和其他脂氧合酶介体的合成。在常驻腹膜巨噬细胞中,二十二碳五烯酸(DPA)负责补充EPA后的环氧合酶抑制作用,从而为EPA如何通过延长至22碳DPA间接发挥抗炎作用提供了新的见解。

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    Department of Chemistry/Biochemistry and Department of Pharmacology, School of Medicine, University of California at San Diego, La Jolla, CA 92093;

    Department of Chemistry/Biochemistry and Department of Pharmacology, School of Medicine, University of California at San Diego, La Jolla, CA 92093;

  • 收录信息 美国《科学引文索引》(SCI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 正文语种 eng
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