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Omega-9 Oleic Acid Induces Fatty Acid Oxidation and Decreases Organ Dysfunction and Mortality in Experimental Sepsis

机译:Omega-9油酸诱导实验性脓毒症中的脂肪酸氧化并降低器官功能障碍和死亡率

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摘要

Sepsis is characterized by inflammatory and metabolic alterations, which lead to massive cytokine production, oxidative stress and organ dysfunction. In severe systemic inflammatory response syndrome, plasma non-esterified fatty acids (NEFA) are increased. Several NEFA are deleterious to cells, activate Toll-like receptors and inhibit Na+/K+-ATPase, causing lung injury. A Mediterranean diet rich in olive oil is beneficial. The main component of olive oil is omega-9 oleic acid (OA), a monounsaturated fatty acid (MUFA). We analyzed the effect of OA supplementation on sepsis. OA ameliorated clinical symptoms, increased the survival rate, prevented liver and kidney injury and decreased NEFA plasma levels in mice subjected to cecal ligation and puncture (CLP). OA did not alter food intake and weight gain but diminished reactive oxygen species (ROS) production and NEFA plasma levels. Carnitine palmitoyltransferase IA (CPT1A) mRNA levels were increased, while uncoupling protein 2 (UCP2) liver expression was enhanced in mice treated with OA. OA also inhibited the decrease in 5' AMP-activated protein kinase (AMPK) expression and increased the enzyme expression in the liver of OA-treated mice compared to septic animals. We showed that OA pretreatment decreased NEFA concentration and increased CPT1A and UCP2 and AMPK levels, decreasing ROS production. We suggest that OA has a beneficial role in sepsis by decreasing metabolic dysfunction, supporting the benefits of diets high in monounsaturated fatty acids (MUFA).
机译:脓毒症的特征在于炎症和代谢改变,其导致大量的细胞因子产生,氧化应激和器官功能障碍。在严重的全身性炎症反应综合征中,血浆非酯化脂肪酸(NEFA)升高。几种NEFA对细胞有害,激活Toll样受体并抑制Na + / K + -ATPase,引起肺损伤。富含橄榄油的地中海饮食是有益的。橄榄油的主要成分是omega-9油酸(OA),一种单不饱和脂肪酸(MUFA)。我们分析了补充OA对败血症的影响。 OA改善了盲肠结扎和穿刺(CLP)小鼠的临床症状,提高了存活率,防止了肝肾损伤,并降低了NEFA血浆水平。 OA不会改变食物摄入和体重增加,但会减少活性氧(ROS)的产生和NEFA血浆水平。在用OA处理的小鼠中,肉碱棕榈酰转移酶IA(CPT1A)mRNA水平增加,而解偶联蛋白2(UCP2)肝脏表达增强。与脓毒症动物相比,OA还抑制OA处理的小鼠肝脏5'AMP激活的蛋白激酶(AMPK)表达的降低,并增加酶的表达。我们表明,OA预处理可降低NEFA浓度并增加CPT1A和UCP2和AMPK水平,从而降低ROS的产生。我们建议OA通过降低代谢功能障碍在败血症中具有有益作用,支持高单不饱和脂肪酸(MUFA)饮食的益处。

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