Environmental toxicology: Sensitive periods of development and neurodevelopmental disorders

被引:154
作者
Heyer, Djai B. [1 ]
Meredith, Rhiannon M. [1 ]
机构
[1] Vrije Univ Amsterdam, Dept Integrat Neurophysiol, CNCR, De Boelelaan 1085, NL-1081 HV Amsterdam, Netherlands
关键词
Neurodevelopmental disorders; Autism; ADHD; Schizophrenia; Toxicant; Prenatal; DEFICIT HYPERACTIVITY DISORDER; AUTISM SPECTRUM DISORDERS; ATTENTION-DEFICIT/HYPERACTIVITY DISORDER; ORGANOPHOSPHATE PESTICIDE EXPOSURE; PRENATAL METHYLMERCURY EXPOSURE; POLYCHLORINATED-BIPHENYLS PCBS; DEVELOPING NERVOUS-SYSTEM; INDUCED OXIDATIVE STRESS; POSTNATAL LEAD-EXPOSURE; URINARY BISPHENOL-A;
D O I
10.1016/j.neuro.2016.10.017
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Development of the mammalian central nervous system is a complex process whose disruption may have severe and long-lasting consequences upon brain structure and function, potentially resulting in a neurodevelopmental disorder (NDD). Many NDDs are known to be genetic in origin, with symptom onset and their underlying mechanisms now known to be regulated during time-dependent windows or 'critical periods' during normal brain development. However, it is increasingly evident that similar disturbances to the developing nervous system may be caused by exposure to non-genetic, environmental factors. Strikingly, at least 200 industrially applied or produced chemicals have been associated with neurotoxicity in humans and exposure to these modifying compounds, through consumer products or environmental pollution, therefore poses serious threats to public health. Through a combination of human epidemiological and animal experimental studies, we identified developmental periods for increased vulnerability to environmentally-modifying compounds and determined whether and how exposure during specific sensitive time-windows could increase the risk for the NDDs of autism, ADHD or schizophrenia in the developing organism. We report that many environmental toxicants have distinct sensitive time-windows during which exposure may disrupt critical developmental events, thereby increasing the risk of developing NDDs. The majority of these time-windows occur prenatally rather than postnatally. We propose four underlying mechanisms that mediate pathogenesis, namely oxidative stress, immune system dysregulation, altered neurotransmission and thyroid hormone disruption. Given the complexity of underlying mechanisms and their prenatal inception, treatment options are currently limited. Thus, we conclude that preventing early exposure to environmental toxicants, by increasing public awareness and improving government and industry guidelines, may ultimately lead to a significant reduction in the incidence of NDDs. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:23 / 41
页数:19
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