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Morphogenetic roles of acetylcholine.

In the adult nervous system, neurotransmitters mediate cellular communication within neuronal circuits. In developing tissues and primitive organisms, neurotransmitters subserve growth regulatory and morphogenetic functions. Accumulated evidence suggests that acetylcholine, (ACh), released from grow...

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Detalles Bibliográficos
Autores principales: Lauder, J M, Schambra, U B
Formato: Texto
Lenguaje:English
Publicado: 1999
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1566361/
https://www.ncbi.nlm.nih.gov/pubmed/10229708
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author Lauder, J M
Schambra, U B
author_facet Lauder, J M
Schambra, U B
author_sort Lauder, J M
collection PubMed
description In the adult nervous system, neurotransmitters mediate cellular communication within neuronal circuits. In developing tissues and primitive organisms, neurotransmitters subserve growth regulatory and morphogenetic functions. Accumulated evidence suggests that acetylcholine, (ACh), released from growing axons, regulates growth, differentiation, and plasticity of developing central nervous system neurons. In addition to intrinsic cholinergic neurons, the cerebral cortex and hippocampus receive extensive innervation from cholinergic neurons in the basal forebrain, beginning prenatally and continuing throughout the period of active growth and synaptogenesis. Acute exposure to ethanol in early gestation (which prevents formation of basal forebrain cholinergic neurons) or neonatal lesioning of basal forebrain cholinergic neurons, significantly compromises cortical development and produces persistent impairment of cognitive functions. Neonatal visual deprivation alters developmental expression of muscarinic acetylcholine receptors (mAChR) in visual cortex, whereas local infusion of mAChR antagonists impairs plasticity of visual cortical neurons. These findings raise the possibility that exposure to environmental neurotoxins that affect cholinergic systems may seriously compromise brain development and have long-lasting morphologic, neurochemical, and functional consequences.
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spelling pubmed-15663612006-09-19 Morphogenetic roles of acetylcholine. Lauder, J M Schambra, U B Environ Health Perspect Research Article In the adult nervous system, neurotransmitters mediate cellular communication within neuronal circuits. In developing tissues and primitive organisms, neurotransmitters subserve growth regulatory and morphogenetic functions. Accumulated evidence suggests that acetylcholine, (ACh), released from growing axons, regulates growth, differentiation, and plasticity of developing central nervous system neurons. In addition to intrinsic cholinergic neurons, the cerebral cortex and hippocampus receive extensive innervation from cholinergic neurons in the basal forebrain, beginning prenatally and continuing throughout the period of active growth and synaptogenesis. Acute exposure to ethanol in early gestation (which prevents formation of basal forebrain cholinergic neurons) or neonatal lesioning of basal forebrain cholinergic neurons, significantly compromises cortical development and produces persistent impairment of cognitive functions. Neonatal visual deprivation alters developmental expression of muscarinic acetylcholine receptors (mAChR) in visual cortex, whereas local infusion of mAChR antagonists impairs plasticity of visual cortical neurons. These findings raise the possibility that exposure to environmental neurotoxins that affect cholinergic systems may seriously compromise brain development and have long-lasting morphologic, neurochemical, and functional consequences. 1999-02 /pmc/articles/PMC1566361/ /pubmed/10229708 Text en
spellingShingle Research Article
Lauder, J M
Schambra, U B
Morphogenetic roles of acetylcholine.
title Morphogenetic roles of acetylcholine.
title_full Morphogenetic roles of acetylcholine.
title_fullStr Morphogenetic roles of acetylcholine.
title_full_unstemmed Morphogenetic roles of acetylcholine.
title_short Morphogenetic roles of acetylcholine.
title_sort morphogenetic roles of acetylcholine.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1566361/
https://www.ncbi.nlm.nih.gov/pubmed/10229708
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