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首页> 外文期刊>Inhalation toxicology >Effects of subchronic exposures to concentrated ambient particles in mice. IX. Integral assessment and human health implications of subchronic exposures of mice to CAPs.
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Effects of subchronic exposures to concentrated ambient particles in mice. IX. Integral assessment and human health implications of subchronic exposures of mice to CAPs.

机译:亚慢性暴露于小鼠集中环境颗粒的影响。九。小鼠亚慢性暴露于CAP的综合评估和对人类健康的影响。

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摘要

In order to examine the biologic plausibility of adverse chronic cardiopulmonary effects in humans associated with ambient particulate matter (PM) exposure, we exposed groups of normal mice (C57) and knockout mice that develop atherosclerotic plaque (ApoE-/- and ApoE-/- LDLr-/-) for 6 h/day, 5 days/wk for 5 or 6 mo during the spring/summer of 2003 to either filtered air or 10-fold concentrated ambient particles (CAPs) in Tuxedo, NY (average PM2.5 concentration during exposure = 110 microg/m3). Some of the mice had implanted electrocardiographic monitors. We demonstrated that: (1) this complex interdisciplinary study was technically feasible in terms of daily exposure, collection of air quality monitoring data, the collection, analysis, and interpretation of continuous data on cardiac function, and the collection and analyses of tissues of the animals sacrificed at the end of the study; (2) the daily variations in CAPs were significantly associated, in ApoE-/- mice, with daily variations in cardiac functions; (3) there were significant differences between CAPs and sham-exposed ApoE-/- mice in terms of cardiac function after the end of exposure period, as well as small differences in atherosclerotic plaque density, coronary artery disease, and cell density in the substantia nigra in the brain in the ApoE-/- mice; (4) there are suggestive indications of gene expression changes for genes associated with the control of circadian rhythm in the ApoE-/- LDLr-/- double knockout (DK) mice. These various CAPs-related effects on cardiac function and the development of histological evidence of increased risk of clinically significant disease at the end of exposures in animal models of atherosclerosis provide biological plausibility for the premature mortality associated with PM2.5 exposure in human subjects and provide suggestive evidence for neurogenic disease as well.
机译:为了检查与环境颗粒物(PM)暴露相关的人类慢性心肺不良反应的生物学可行性,我们暴露了正常小鼠(C57)和敲除小鼠形成动脉粥样硬化斑块(ApoE-/-和ApoE-/- LDLr-/-)在2003年春季/夏季连续6小时/天,5天/周,5天/周,以过滤空气或纽约州Tuxedo的10倍浓缩环境颗粒(CAPs)(平均PM2.5)暴露过程中的浓度= 110微克/立方米)。一些小鼠植入了心电监护仪。我们证明:(1)这项复杂的跨学科研究在日常暴露,空气质量监测数据的收集,心脏功能连续数据的收集,分析和解释,以及心脏组织的收集和分析方面在技术上是可行的。研究结束时处死的动物; (2)在ApoE-/-小鼠中,CAPs的每日变化与心脏功能的每日变化显着相关; (3)在暴露期结束后,CAPs和假暴露的ApoE-/-小鼠在心功能方面存在显着差异,并且在实体层中,动脉粥样硬化斑块密度,冠状动脉疾病和细胞密度也存在细微差异ApoE-/-小鼠大脑中的黑质; (4)在ApoE-/-LDLr-/-双敲除(DK)小鼠中,与昼夜节律控制相关的基因的基因表达发生了改变。在动脉粥样硬化动物模型中,这些与CAPs相关的各种对心脏功能的影响以及在暴露结束时临床显着疾病风险增加的组织学证据的发展为人类受试者与PM2.5暴露相关的过早死亡提供了生物学上的合理性,并提供了神经源性疾病的暗示证据。

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