Office of Environmental Health Hazard Assessment, California Environmental Protection Agency, Oakland, California, USA.
Environ Health Perspect. 2010 Aug;118(8):1155-64. doi: 10.1289/ehp.0901856. Epub 2010 May 5.
Disruption of fundamental biologic processes and associated signaling events may result in clinically significant alterations in lung development.
We reviewed evidence on the impact of environmental chemicals on lung development and key signaling events in lung morphogenesis, and the relevance of potential outcomes to public health and regulatory science .
We evaluated the peer-reviewed literature on developmental lung biology and toxicology, mechanistic studies, and supporting epidemiology.
Lung function in infancy predicts pulmonary function throughout life. In utero and early postnatal exposures influence both childhood and adult lung structure and function and may predispose individuals to chronic obstructive lung disease and other disorders. The nutritional and endogenous chemical environment affects development of the lung and can result in altered function in the adult. Studies now suggest that similar adverse impacts may occur in animals and humans after exposure to environmentally relevant doses of certain xenobiotics during critical windows in early life. Potential mechanisms include interference with highly conserved factors in developmental processes such as gene regulation, molecular signaling, and growth factors involved in branching morphogenesis and alveolarization.
Assessment of environmental chemical impacts on the lung requires studies that evaluate specific alterations in structure or function-end points not regularly assessed in standard toxicity tests. Identifying effects on important signaling events may inform protocols of developmental toxicology studies. Such knowledge may enable policies promoting true primary prevention of lung diseases. Evidence of relevant signaling disruption in the absence of adequate developmental toxicology data should influence the size of the uncertainty factors used in risk assessments.
基本生物过程和相关信号事件的破坏可能导致肺发育的临床显著改变。
我们回顾了环境化学物质对肺发育和肺形态发生中关键信号事件的影响,以及潜在结果与公共卫生和监管科学的相关性。
我们评估了关于发育肺生物学和毒理学、机制研究以及支持性流行病学的同行评议文献。
婴儿期的肺功能预测整个生命周期的肺功能。宫内和产后早期暴露会影响儿童和成人的肺结构和功能,并可能使个体易患慢性阻塞性肺病和其他疾病。营养和内源性化学环境会影响肺的发育,并导致成年后功能改变。现在的研究表明,在生命早期的关键窗口期,接触环境相关剂量的某些外源化学物质后,动物和人类可能会出现类似的不良影响。潜在的机制包括干扰基因调控、分子信号和参与分支形态发生和肺泡化的生长因子等发育过程中的高度保守因子。
评估环境化学物质对肺的影响需要研究评估结构或功能终点的特定改变,这些改变通常不在标准毒性测试中评估。确定对重要信号事件的影响可能为发育毒理学研究的方案提供信息。这种知识可能使促进真正的肺部疾病一级预防的政策成为可能。在缺乏充分的发育毒理学数据的情况下,有证据表明相关信号中断,应影响风险评估中使用的不确定因素的大小。