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Diesel and biodiesel exhaust particle effects on rat alveolar macrophages with in vitro exposure

机译:体外暴露对大鼠肺泡巨噬细胞的柴油和生物柴油尾气颗粒影响

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摘要

Combustion emissions from diesel engines emit particulate matter which deposits within the lungs. Alveolar macrophages (AM) encounter the particles and attempt to engulf the particles. Emissions particles from diesel combustion engines have been found to contain diverse biologically active components including metals and polyaromatic hydrocarbons which cause adverse health effects. However little is known about AM response to particles from the incorporation of biodiesel. The objective of this study was to examine the toxicity in Wistar Kyoto rat AM of biodiesel blend (B20) and low sulfur petroleum diesel (PDEP) exhaust particles. Particles were independently suspended in media at a range of 1–500µg/mL. Results indicated B20 and PDEP initiated a dose dependent increase of inflammatory signals from AM after exposure. After 24hr exposure to B20 and PDEP gene expression of cyclooxygenase-2 (COX-2) and macrophage inflammatory protein 2 (MIP-2) increased. B20 exposure resulted in elevated prostaglandin E2 (PGE2) release at lower particle concentrations compared to PDEP. B20 and PDEP demonstrated similar affinity for sequesteration of PGE2 at high concentrations, suggesting detection is not imparied. Our data suggests PGE2 release from AM is dependent on the chemical composition of the particles. Particle analysis including measurments of metals and ions indicate B20 contains more of select metals than PDEP. Other particle components generally reduced by 20% with 20% incoporation of biodiesel into original diesel. This study shows AM exposure to B20 results in increased production of PGE2 in vitro relative to diesel.
机译:柴油发动机的燃烧排放物排放了沉积在肺部的颗粒物。肺泡巨噬细胞(AM)遇到颗粒并试图吞噬颗粒。已经发现柴油内燃机的排放颗粒含有多种生物活性成分,包括对健康造成不利影响的金属和聚芳烃。然而,关于掺入生物柴油的AM对颗粒的反应知之甚少。这项研究的目的是研究生物柴油混合物(B20)和低硫石油柴油(PDEP)排气颗粒在Wistar Kyoto Rat AM中的毒性。颗粒以1–500µg / mL的范围独立悬浮在培养基中。结果表明,B20和PDEP在暴露后会引发AM引起的炎症信号剂量依赖性增加。暴露于B20和PDEP 24小时后,环氧合酶2(COX-2)和巨噬细胞炎症蛋白2(MIP-2)的表达增加。与PDEP相比,B20暴露导致在较低的颗粒浓度下升高的前列腺素E2(PGE2)释放。 B20和PDEP在高浓度下对螯合PGE2表现出相似的亲和力,表明检测没有障碍。我们的数据表明,AM中PGE2的释放取决于颗粒的化学组成。包括金属和离子测量在内的颗粒分析表明,B20比PDEP含有更多的精选金属。随着20%的生物柴油掺入原始柴油中,其他颗粒成分通常减少20%。这项研究表明,与柴油相比,AM暴露于B20会导致体外增加PGE2的产生。

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