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Extra virgin olive oil polyphenolic extracts downregulate inflammatory responses in LPS-activated murine peritoneal macrophages suppressing NF kappaB and MAPK signalling pathways.

机译:特级初榨橄榄油多酚提取物下调LPS激活的鼠腹膜巨噬细胞中的炎症反应,从而抑制NF kappaB和MAPK信号通路。

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摘要

Extra virgin olive oil (EVOO) is obtained from the fruit of the olive tree Olea europaea L. Phenolic compounds present in EVOO have recognized anti-oxidant and anti-inflammatory properties. However, the activity of the total phenolic fraction extracted from EVOO and the action mechanisms involved are not well defined. The present study was designed to evaluate the potential anti-inflammatory mechanisms of the polyphenolic extract (PE) from EVOO on LPS-stimulated peritoneal murine macrophages. Nitric oxide (NO) production was analyzed by the Griess method and intracellular reactive oxygen species (ROS) by fluorescence analysis. Moreover, changes in the protein expression of the pro-inflammatory enzymes, inducible nitric oxide synthase (iNOS), cyclooxygenase (COX)-2 and microsomal prostaglandin E synthase-1 (mPGES-1), as well as the role of nuclear transcription factor kappa B (NF kappaB) and mitogen-activated protein kinase (MAPK) signalling pathways, were analyzed by Western blot. PE from EVOO reduced LPS-induced oxidative stress and inflammatory responses through decreasing NO and ROS generation. In addition, PE induced a significant down-regulation of iNOS, COX-2 and mPGES-1 protein expressions, reduced MAPK phosphorylation and prevented the nuclear NF kappaB translocation. This study establishes that PE from EVOO possesses anti-inflammatory activities on LPS-stimulated murine macrophages.
机译:特级初榨橄榄油(EVOO)是从橄榄树Olea europaea L的果实中获得的。EVOO中存在的酚类化合物具有公认的抗氧化剂和抗炎特性。但是,从EVOO中提取的总酚类馏分的活性和涉及的作用机理尚不清楚。本研究旨在评估EVOO中多酚提取物(PE)对LPS刺激的腹膜鼠巨噬细胞的潜在抗炎机制。通过Griess方法分析一氧化氮(NO)的产生,并通过荧光分析分析细胞内活性氧(ROS)。此外,促炎酶,诱导型一氧化氮合酶(iNOS),环氧合酶(COX)-2和微粒体前列腺素E合酶-1(mPGES-1)的蛋白质表达以及核转录因子的作用也发生了变化。蛋白质印迹分析了κB(NF kappaB)和有丝分裂原激活的蛋白激酶(MAPK)信号通路。 EVOO中的PE通过减少NO和ROS的生成来降低LPS诱导的氧化应激和炎症反应。此外,PE诱导iNOS,COX-2和mPGES-1蛋白表达显着下调,降低MAPK磷酸化并阻止核NF kappaB移位。这项研究表明,EVOO中的PE对LPS刺激的鼠巨噬细胞具有抗炎活性。

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