Constructing an adverse outcome pathway framework for the impact of maternal exposure to PM2.5 on liver development and injury in offspring

IF 4.2 3区 环境科学与生态学 Q2 ENVIRONMENTAL SCIENCES Environmental toxicology and pharmacology Pub Date : 2024-11-01 DOI:10.1016/j.etap.2024.104585
Kexin Zhang , Li Tian , Qinglin Sun , Jianong Lv , Ruiyang Ding , Yang Yu , Yang Li , Junchao Duan
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Abstract

Ambient fine particulate matter (PM2.5) is a significant contributor to air pollution. PM2.5 exposure poses a substantial hazard to public health. In recent years, the adverse effects of maternal PM2.5 exposure on fetal health have gradually gained public attention. As the largest organ in the body, the liver has many metabolic and secretory functions. Liver development, as well as factors that interfere with its growth and function, are of concern. This review utilized the adverse outcome pathway (AOP) framework as the analytical approach to demonstrate the link between maternal PM2.5 exposure and potential neonatal liver injury from the molecular to the population level. The excessive generation of reactive oxygen species (ROS), subsequent endoplasmic reticulum (ER) stress, and oxidative stress were regarded as the essential components in this framework, as they could trigger adverse developmental outcomes in the offspring through DNA damage, autophagy dysfunction, mitochondrial injury, and other pathways. To the best of our knowledge, this is the first article based on an AOP framework that elaborates on the influence of maternal exposure to PM2.5 on liver injury occurrence and adverse effects on liver development in offspring. Therefore, this review offered mechanistic insights into the developmental toxicity of PM2.5 in the liver, which provided a valuable basis for future studies and prevention strategies.
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构建母体暴露于 PM2.5 对后代肝脏发育和损伤影响的不良后果路径框架。
环境细颗粒物(PM2.5)是造成空气污染的重要因素。暴露于 PM2.5 会对公众健康造成巨大危害。近年来,母体暴露于PM2.5对胎儿健康的不良影响逐渐受到公众的关注。作为人体最大的器官,肝脏具有多种代谢和分泌功能。肝脏的发育以及干扰其生长和功能的因素都值得关注。本综述利用不良后果途径(AOP)框架作为分析方法,从分子到人群层面论证了母体接触 PM2.5 与新生儿潜在肝损伤之间的联系。活性氧(ROS)的过度生成、随后的内质网(ER)应激和氧化应激被认为是这一框架的重要组成部分,因为它们可能通过DNA损伤、自噬功能障碍、线粒体损伤和其他途径引发后代的不良发育结果。据我们所知,这是第一篇基于AOP框架阐述母体暴露于PM2.5对肝损伤发生的影响以及对后代肝脏发育不良影响的文章。因此,这篇综述从机理上揭示了PM2.5对肝脏发育的毒性,为今后的研究和预防策略提供了宝贵的依据。
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来源期刊
CiteScore
7.00
自引率
4.70%
发文量
185
审稿时长
34 days
期刊介绍: Environmental Toxicology and Pharmacology publishes the results of studies concerning toxic and pharmacological effects of (human and veterinary) drugs and of environmental contaminants in animals and man. Areas of special interest are: molecular mechanisms of toxicity, biotransformation and toxicokinetics (including toxicokinetic modelling), molecular, biochemical and physiological mechanisms explaining differences in sensitivity between species and individuals, the characterisation of pathophysiological models and mechanisms involved in the development of effects and the identification of biological markers that can be used to study exposure and effects in man and animals. In addition to full length papers, short communications, full-length reviews and mini-reviews, Environmental Toxicology and Pharmacology will publish in depth assessments of special problem areas. The latter publications may exceed the length of a full length paper three to fourfold. A basic requirement is that the assessments are made under the auspices of international groups of leading experts in the fields concerned. The information examined may either consist of data that were already published, or of new data that were obtained within the framework of collaborative research programmes. Provision is also made for the acceptance of minireviews on (classes of) compounds, toxicities or mechanisms, debating recent advances in rapidly developing fields that fall within the scope of the journal.
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