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Effects of 514-HEDGE a 20-HETE mimetic on lipopolysaccharide-induced changes in MyD88/TAK1/IKKβ/IκB-α/NF-κB pathway and circulating miR-150 miR-223 and miR-297 levels in a rat model of septic shock

机译:模仿20-HETE的514-HEDGE对脂多糖诱导的MyD88 / TAK1 /IKKβ/IκB-α/NF-κB途径变化以及循环中的miR-150miR-223和miR-297水平的影响败血性休克的大鼠模型

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摘要

ObjectivesWe have previously demonstrated that a stable synthetic analog of 20-hydroxyeicosatetraenoic acid (20-HETE), N-(20-hydroxyeicosa-5[Z],14[Z]-dienoyl)glycine (5,14-HEDGE), which mimics the effects of endogenously produced 20-HETE, prevents vascular hyporeactivity, hypotension, tachycardia, inflammation, and mortality in a rodent model of septic shock. The present study was performed to determine whether decreased renal and cardiovascular expression and activity of myeloid differentiation factor 88 (MyD88)/transforming growth factor-activated kinase 1 (TAK1)/inhibitor of κB (IκB) kinase β (IKKβ)/IκB-αuclear factor-κB (NF-κB) pathway and reduced circulating microRNA (miR)-150, miR-223, and miR-297 expression levels participate in the protective effect of 5,14-HEDGE against hypotension, tachycardia, and inflammation in response to systemic administration of lipopolysaccharide (LPS).
机译:目的我们先前已经证明了一种稳定的20-羟基二十碳四烯酸(20-HETE),N-(20-羟基二十碳五[Z],14 [Z]-二烯酰基)甘氨酸(5,14-HEDGE)的合成类似物内源性20-HETE的作用可预防败血性休克啮齿动物模型中的血管反应性低下,低血压,心动过速,炎症和死亡。本研究的目的是确定是否降低了肾脏和心血管的表达以及髓系分化因子88(MyD88)/转化生长因子激活激酶1(TAK1)/κB(IκB)激酶β(IKKβ)/IκB-α抑制剂的活性/核因子-κB(NF-κB)通路和循环微RNA(miR)-150,miR-223和miR-297表达水平降低参与了5,14-HEDGE对低血压,心动过速和炎症的保护作用对脂多糖(LPS)全身给药的反应。

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