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The mouse olfactory peduncle. 3. Development of neurons, glia, and centrifugal afferents

The present series of studies was designed to provide a general overview of the development of the region connecting the olfactory bulb to the forebrain. The olfactory peduncle (OP) contains several structures involved in processing odor information with the anterior olfactory nucleus (cortex) being...

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Autores principales: Brunjes, Peter C., Collins, Lindsay N., Osterberg, Stephen K., Phillips, Adriana M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4046489/
https://www.ncbi.nlm.nih.gov/pubmed/24926238
http://dx.doi.org/10.3389/fnana.2014.00044
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author Brunjes, Peter C.
Collins, Lindsay N.
Osterberg, Stephen K.
Phillips, Adriana M.
author_facet Brunjes, Peter C.
Collins, Lindsay N.
Osterberg, Stephen K.
Phillips, Adriana M.
author_sort Brunjes, Peter C.
collection PubMed
description The present series of studies was designed to provide a general overview of the development of the region connecting the olfactory bulb to the forebrain. The olfactory peduncle (OP) contains several structures involved in processing odor information with the anterior olfactory nucleus (cortex) being the largest and most studied. Results indicate that considerable growth occurs in the peduncle from postnatal day (P)10–P20, with reduced expansion from P20 to P30. No evidence was found for the addition of new projection or interneurons during the postnatal period. GABAergic cells decreased in both number and density after P10. Glial populations exhibited different patterns of development, with astrocytes declining in density from P10 to P30, and both oligodendrocytes and microglia increasing through the interval. Myelination in the anterior commissure emerged between P11 and P14. Dense cholinergic innervation was observed at P10 and remained relatively stable through P30, while considerable maturation of serotonergic innervation occurred through the period. Unilateral naris occlusion from P1 to P30 resulted in about a 30% reduction in the size of the ipsilateral peduncle but few changes were observed on the contralateral side. The ipsilateral peduncle also exhibited higher densities of GAD67-containing interneurons and cholinergic fibers suggesting a delay in normal developmental pruning. Lower densities of interneurons expressing CCK, somatostatin, and NPY and in myelin basic protein staining were also observed. Understanding variations in developmental trajectories within the OP may be an important tool for unraveling the functions of the region.
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spelling pubmed-40464892014-06-12 The mouse olfactory peduncle. 3. Development of neurons, glia, and centrifugal afferents Brunjes, Peter C. Collins, Lindsay N. Osterberg, Stephen K. Phillips, Adriana M. Front Neuroanat Neuroscience The present series of studies was designed to provide a general overview of the development of the region connecting the olfactory bulb to the forebrain. The olfactory peduncle (OP) contains several structures involved in processing odor information with the anterior olfactory nucleus (cortex) being the largest and most studied. Results indicate that considerable growth occurs in the peduncle from postnatal day (P)10–P20, with reduced expansion from P20 to P30. No evidence was found for the addition of new projection or interneurons during the postnatal period. GABAergic cells decreased in both number and density after P10. Glial populations exhibited different patterns of development, with astrocytes declining in density from P10 to P30, and both oligodendrocytes and microglia increasing through the interval. Myelination in the anterior commissure emerged between P11 and P14. Dense cholinergic innervation was observed at P10 and remained relatively stable through P30, while considerable maturation of serotonergic innervation occurred through the period. Unilateral naris occlusion from P1 to P30 resulted in about a 30% reduction in the size of the ipsilateral peduncle but few changes were observed on the contralateral side. The ipsilateral peduncle also exhibited higher densities of GAD67-containing interneurons and cholinergic fibers suggesting a delay in normal developmental pruning. Lower densities of interneurons expressing CCK, somatostatin, and NPY and in myelin basic protein staining were also observed. Understanding variations in developmental trajectories within the OP may be an important tool for unraveling the functions of the region. Frontiers Media S.A. 2014-06-05 /pmc/articles/PMC4046489/ /pubmed/24926238 http://dx.doi.org/10.3389/fnana.2014.00044 Text en Copyright © 2014 Brunjes, Collins, Osterberg and Phillips. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Brunjes, Peter C.
Collins, Lindsay N.
Osterberg, Stephen K.
Phillips, Adriana M.
The mouse olfactory peduncle. 3. Development of neurons, glia, and centrifugal afferents
title The mouse olfactory peduncle. 3. Development of neurons, glia, and centrifugal afferents
title_full The mouse olfactory peduncle. 3. Development of neurons, glia, and centrifugal afferents
title_fullStr The mouse olfactory peduncle. 3. Development of neurons, glia, and centrifugal afferents
title_full_unstemmed The mouse olfactory peduncle. 3. Development of neurons, glia, and centrifugal afferents
title_short The mouse olfactory peduncle. 3. Development of neurons, glia, and centrifugal afferents
title_sort mouse olfactory peduncle. 3. development of neurons, glia, and centrifugal afferents
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4046489/
https://www.ncbi.nlm.nih.gov/pubmed/24926238
http://dx.doi.org/10.3389/fnana.2014.00044
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