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Critical periods of vulnerability for the developing nervous system: evidence from humans and animal models.

Vulnerable periods during the development of the nervous system are sensitive to environmental insults because they are dependent on the temporal and regional emergence of critical developmental processes (i.e., proliferation, migration, differentiation, synaptogenesis, myelination, and apoptosis)....

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Detalles Bibliográficos
Autores principales: Rice, D, Barone, S
Formato: Texto
Lenguaje:English
Publicado: 2000
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1637807/
https://www.ncbi.nlm.nih.gov/pubmed/10852851
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author Rice, D
Barone, S
author_facet Rice, D
Barone, S
author_sort Rice, D
collection PubMed
description Vulnerable periods during the development of the nervous system are sensitive to environmental insults because they are dependent on the temporal and regional emergence of critical developmental processes (i.e., proliferation, migration, differentiation, synaptogenesis, myelination, and apoptosis). Evidence from numerous sources demonstrates that neural development extends from the embryonic period through adolescence. In general, the sequence of events is comparable among species, although the time scales are considerably different. Developmental exposure of animals or humans to numerous agents (e.g., X-ray irradiation, methylazoxymethanol, ethanol, lead, methyl mercury, or chlorpyrifos) demonstrates that interference with one or more of these developmental processes can lead to developmental neurotoxicity. Different behavioral domains (e.g., sensory, motor, and various cognitive functions) are subserved by different brain areas. Although there are important differences between the rodent and human brain, analogous structures can be identified. Moreover, the ontogeny of specific behaviors can be used to draw inferences regarding the maturation of specific brain structures or neural circuits in rodents and primates, including humans. Furthermore, various clinical disorders in humans (e.g., schizophrenia, dyslexia, epilepsy, and autism) may also be the result of interference with normal ontogeny of developmental processes in the nervous system. Of critical concern is the possibility that developmental exposure to neurotoxicants may result in an acceleration of age-related decline in function. This concern is compounded by the fact that developmental neurotoxicity that results in small effects can have a profound societal impact when amortized across the entire population and across the life span of humans.
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spelling pubmed-16378072006-11-17 Critical periods of vulnerability for the developing nervous system: evidence from humans and animal models. Rice, D Barone, S Environ Health Perspect Research Article Vulnerable periods during the development of the nervous system are sensitive to environmental insults because they are dependent on the temporal and regional emergence of critical developmental processes (i.e., proliferation, migration, differentiation, synaptogenesis, myelination, and apoptosis). Evidence from numerous sources demonstrates that neural development extends from the embryonic period through adolescence. In general, the sequence of events is comparable among species, although the time scales are considerably different. Developmental exposure of animals or humans to numerous agents (e.g., X-ray irradiation, methylazoxymethanol, ethanol, lead, methyl mercury, or chlorpyrifos) demonstrates that interference with one or more of these developmental processes can lead to developmental neurotoxicity. Different behavioral domains (e.g., sensory, motor, and various cognitive functions) are subserved by different brain areas. Although there are important differences between the rodent and human brain, analogous structures can be identified. Moreover, the ontogeny of specific behaviors can be used to draw inferences regarding the maturation of specific brain structures or neural circuits in rodents and primates, including humans. Furthermore, various clinical disorders in humans (e.g., schizophrenia, dyslexia, epilepsy, and autism) may also be the result of interference with normal ontogeny of developmental processes in the nervous system. Of critical concern is the possibility that developmental exposure to neurotoxicants may result in an acceleration of age-related decline in function. This concern is compounded by the fact that developmental neurotoxicity that results in small effects can have a profound societal impact when amortized across the entire population and across the life span of humans. 2000-06 /pmc/articles/PMC1637807/ /pubmed/10852851 Text en
spellingShingle Research Article
Rice, D
Barone, S
Critical periods of vulnerability for the developing nervous system: evidence from humans and animal models.
title Critical periods of vulnerability for the developing nervous system: evidence from humans and animal models.
title_full Critical periods of vulnerability for the developing nervous system: evidence from humans and animal models.
title_fullStr Critical periods of vulnerability for the developing nervous system: evidence from humans and animal models.
title_full_unstemmed Critical periods of vulnerability for the developing nervous system: evidence from humans and animal models.
title_short Critical periods of vulnerability for the developing nervous system: evidence from humans and animal models.
title_sort critical periods of vulnerability for the developing nervous system: evidence from humans and animal models.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1637807/
https://www.ncbi.nlm.nih.gov/pubmed/10852851
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