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Impaired vascular function after exposure to diesel exhaust generated at urban transient running conditions

机译:暴露于城市瞬态运行条件下产生的柴油机废气后血管功能受损

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Background Traffic emissions including diesel engine exhaust are associated with increased respiratory and cardiovascular morbidity and mortality. Controlled human exposure studies have demonstrated impaired vascular function after inhalation of exhaust generated by a diesel engine under idling conditions. Objectives To assess the vascular and fibrinolytic effects of exposure to diesel exhaust generated during urban-cycle running conditions that mimic ambient 'real-world' exposures. Methods In a randomised double-blind crossover study, eighteen healthy male volunteers were exposed to diesel exhaust (approximately 250 μg/m3) or filtered air for one hour during intermittent exercise. Diesel exhaust was generated during the urban part of the standardized European Transient Cycle. Six hours post-exposure, vascular vasomotor and fibrinolytic function was assessed during venous occlusion plethysmography with intra-arterial agonist infusions. Measurements and Main Results Forearm blood flow increased in a dose-dependent manner with both endothelial-dependent (acetylcholine and bradykinin) and endothelial-independent (sodium nitroprusside and verapamil) vasodilators. Diesel exhaust exposure attenuated the vasodilatation to acetylcholine (P Conclusion Exposure to diesel exhaust generated under transient running conditions, as a relevant model of urban air pollution, impairs vasomotor function and endogenous fibrinolysis in a similar way as exposure to diesel exhaust generated at idling. This indicates that adverse vascular effects of diesel exhaust inhalation occur over different running conditions with varying exhaust composition and concentrations as well as physicochemical particle properties. Importantly, exposure to diesel exhaust under ETC conditions was also associated with a novel finding of impaired of calcium channel-dependent vasomotor function. This implies that certain cardiovascular endpoints seem to be related to general diesel exhaust properties, whereas the novel calcium flux-related effect may be associated with exhaust properties more specific for the ETC condition, for example a higher content of diesel soot particles along with their adsorbed organic compounds.
机译:背景技术包括柴油发动机排气在内的交通排放与呼吸和心血管疾病和死亡率的增加有关。受控的人体暴露研究表明,在怠速工况下,吸入柴油发动机产生的废气后,血管功能受损。目的评估暴露在模拟环境“真实世界”暴露的城市循环运行条件下产生的柴油机废气对血管和纤维蛋白溶解的影响。方法在一项随机双盲交叉研究中,十八名健康男性志愿者在暴露期间暴露于柴油机废气(约250μg/ m 3 )或过滤空气中一小时。间歇运动。柴油废气是在标准化欧洲瞬态循环的城市部分产生的。暴露后六小时,在静脉闭塞体积描记术中通过动脉内激动剂输注评估了血管舒缩功能和纤溶功能。测量结果和主要结果使用内皮依赖性(乙酰胆碱和缓激肽)和非内皮依赖性(硝普钠和维拉帕米钠)血管扩张剂,前臂血流量呈剂量依赖性增加。柴油机废气暴露减弱了乙酰胆碱的血管舒张作用(P结论作为城市空气污染的一种相关模型,在瞬态运行条件下暴露于柴油机废气中会损害血管舒缩功能和内源性纤维蛋白溶解,其作用类似于在空转时暴露于柴油机废气中。表明在不同的运行条件下,不同的排气成分和浓度以及理化颗粒性质会产生柴油机废气吸入的不利血管作用,重要的是,在ETC条件下暴露于柴油机废气中还发现了钙通道依赖性受损的新发现。血管舒缩功能,这意味着某些心血管终点似乎与一般的柴油机排气特性有关,而新颖的钙通量相关效应可能与对ETC条件更特定的排气特性有关,例如,沿烟气中柴油烟灰颗粒含量更高与它们吸附的有机化合物。

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