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Environmental toxicology: Sensitive periods of development and neurodevelopmental disorders
Djai B Heyer1, Rhiannon M Meredith1
1Department of Integrative Neurophysiology, Center for Neurogenomics and Cognitive Research (CNCR), VU University Amsterdam, De Boelelaan 1085, 1081 HV Amsterdam, The Netherlands.
Abstract:
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.
Insights
Environmental toxicants can disrupt brain development during critical windows, increasing the risk of neurodevelopmental disorders (NDDs) like autism and ADHD. Prevention through reduced exposure is key, as treatments are limited.
Area of Science:
- Neuroscience
- Environmental Health
- Developmental Biology
Background:
- Neurodevelopmental disorders (NDDs) arise from disruptions in central nervous system development.
- While genetic factors are known, environmental exposures are increasingly implicated in NDDs.
- Hundreds of industrial chemicals are linked to neurotoxicity, posing public health risks.
Purpose of the Study:
- Identify critical developmental windows of vulnerability to environmental toxicants.
- Determine if exposure during these windows increases NDD risk (autism, ADHD, schizophrenia).
- Investigate underlying mechanisms of environmentally-induced neurodevelopmental pathogenesis.
Main Methods:
- Combined human epidemiological and animal experimental studies.
- Identified sensitive time-windows for environmental toxicant exposure.
- Analyzed potential mechanisms including oxidative stress, immune dysregulation, neurotransmission alteration, and thyroid hormone disruption.
Main Results:
- Environmental toxicants exhibit distinct sensitive windows during development, primarily prenatal.
- Exposure during these windows elevates the risk of developing NDDs.
- Four key mechanisms mediate pathogenesis: oxidative stress, immune dysregulation, altered neurotransmission, and thyroid hormone disruption.
Conclusions:
- Prenatal exposure to environmental toxicants is a significant risk factor for NDDs.
- Limited treatment options necessitate a focus on prevention.
- Public awareness and improved regulations are crucial to reduce early toxicant exposure and NDD incidence.
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