Liu Shan, Huang Qingyu, Zhang Xi, Dong Wei, Zhang Wenlou, Wu Shaowei, Yang Di, Nan Bingru, Zhang Jie, Shen Heqing, Guo Xinbiao, Deng Furong
Department of Occupational and Environmental Health Sciences, School of Public Health, Peking University, Beijing 100191, China.
Key Laboratory of Urban Environment and Health, Institute of Urban Environment, Chinese Academy of Sciences, Xiamen 361021, China.
Innovation (Camb). 2021 Feb 5;2(1):100087. doi: 10.1016/j.xinn.2021.100087. eCollection 2021 Feb 28.
Ozone is one of the major gaseous pollutants associated with short-term adverse cardiopulmonary effects, even at concentrations below the current indoor air quality limits. However, the underlying biological mechanisms of cardiorespiratory changes with exposure to ozone remain unclear. To further explore molecular linkages between indoor ozone exposure and relevant cardiorespiratory effects, a repeated-measure panel study including 46 schoolchildren was conducted and real-time exposure measurements including ozone were performed inside classrooms every weekday during the study period. Repeated health measurements and urine sample collection were conducted in each participant. Ultra-high-performance liquid chromatography/tandem mass spectrometry and meet-in-metabolite approach were used in metabolomics analysis. Methods including mixed-effect models were adopted to identify metabolites associated with ozone exposure or health indices. Nine metabolites were found to be associated with ozone after mixed-effect model analysis, which are mainly involved in amino acid and bile acid metabolism. Boys may have a greater decrease in bile acid and RNA related metabolites. Four of the nine ozone-related metabolites were also associated with cardiorespiratory function indices. Furthermore, 26.67% of the positive association between ozone and heart rate was mediated by cholestane-3,7,12,25-tetrol-3-glucuronide. Exposure to ozone below the current indoor standards was associated with the deteriorated cardiovascular function by disturbing bile acid and endogenous nitric oxide-related oxidation and inflammation, and associated with the exacerbated airway inflammation by reducing GPx-related anti-oxidation. The results provide metabolic evidence of the cardiorespiratory effects of indoor ozone exposure. Indoor ozone pollution should be controlled further, and more attention should be paid to preventing its adverse health effects, especially in children.
臭氧是与短期不良心肺效应相关的主要气态污染物之一,即使在浓度低于当前室内空气质量限值的情况下也是如此。然而,接触臭氧后心肺变化的潜在生物学机制仍不清楚。为了进一步探索室内臭氧暴露与相关心肺效应之间的分子联系,开展了一项包括46名学童的重复测量面板研究,并在研究期间的每个工作日在教室内进行了包括臭氧在内的实时暴露测量。对每位参与者进行了重复的健康测量和尿液样本采集。代谢组学分析采用超高效液相色谱/串联质谱法和代谢物相遇法。采用包括混合效应模型在内的方法来识别与臭氧暴露或健康指标相关的代谢物。混合效应模型分析后发现有9种代谢物与臭氧相关,主要涉及氨基酸和胆汁酸代谢。男孩胆汁酸和RNA相关代谢物的下降可能更大。9种与臭氧相关的代谢物中有4种也与心肺功能指标相关。此外,臭氧与心率之间26.67%的正相关是由胆甾烷-3,7,12,25-四醇-3-葡萄糖醛酸苷介导的。接触低于当前室内标准的臭氧会通过干扰胆汁酸和内源性一氧化氮相关的氧化和炎症而导致心血管功能恶化,并通过降低与谷胱甘肽过氧化物酶相关的抗氧化作用而加剧气道炎症。这些结果为室内臭氧暴露的心肺效应提供了代谢证据。应进一步控制室内臭氧污染,并且应更加关注预防其对健康的不良影响,尤其是对儿童的影响。