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来自沙特阿拉伯的颗粒物会诱导与炎症、代谢综合征和动脉粥样硬化有关的基因。

Particulate matter from Saudi Arabia induces genes involved in inflammation, metabolic syndrome and atherosclerosis.

机构信息

a Department of Environmental Medicine , NYU School of Medicine , New York , New York , USA.

出版信息

J Toxicol Environ Health A. 2014;77(13):751-66. doi: 10.1080/15287394.2014.892446.

Abstract

Airborne particulate matter (PM) exposure is a major environmental health concern and is linked to metabolic disorders, such as cardiovascular diseases (CVD) and diabetes, which are on the rise in the Kingdom of Saudi Arabia. This study investigated changes in mouse lung gene expression produced by administration of PM10 collected from Jeddah, Saudi Arabia. FVB/N mice were exposed to 100 μg PM10 or water by aspiration and euthanized 24 h later. The bronchoalveolar lavage fluid (BALF) was collected and analyzed for neutrophil concentration and tumor necrosis factor (TNF)-α and interleukin (IL)-6 levels. RNA was extracted from lungs and whole transcript was analyzed using Affymetrix Mouse Gene 1.0 ST Array. Mice exposed to PM10 displayed an increase in neutrophil concentration and elevated TNF-α and IL-6 levels. Gene expression analysis revealed that mice exposed to PM10 displayed 202 genes that were significantly upregulated and 40 genes that were significantly downregulated. PM10 induced genes involved in inflammation, cholesterol and lipid metabolism, and atherosclerosis. This is the first study to demonstrate that Saudi Arabia PM10 increases in vivo expression of genes located in pathways associated with diseases involving metabolic syndrome and atherosclerosis.

摘要

空气中的悬浮颗粒物(PM)暴露是一个主要的环境健康问题,与代谢紊乱有关,如心血管疾病(CVD)和糖尿病,在沙特阿拉伯王国呈上升趋势。本研究调查了沙特阿拉伯吉达市采集的 PM10 对小鼠肺部基因表达的影响。FVB/N 小鼠通过吸入暴露于 100μg PM10 或水,24 小时后处死。收集支气管肺泡灌洗液(BALF)并分析中性粒细胞浓度以及肿瘤坏死因子(TNF)-α和白细胞介素(IL)-6 水平。从肺部提取 RNA,并使用 Affymetrix Mouse Gene 1.0 ST Array 进行全转录分析。暴露于 PM10 的小鼠显示中性粒细胞浓度增加,TNF-α和 IL-6 水平升高。基因表达分析显示,暴露于 PM10 的小鼠有 202 个基因显著上调,40 个基因显著下调。PM10 诱导的基因参与炎症、胆固醇和脂质代谢以及动脉粥样硬化。这是第一项表明沙特阿拉伯 PM10 增加与代谢综合征和动脉粥样硬化相关疾病途径中基因表达的体内研究。

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