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Substance P NK1 receptor in the rat corpus callosum during postnatal development
INTRODUCTION: The expression of substance P (SP) receptor (neurokinin 1, NK1) was studied in the rat corpus callosum (cc) from postnatal day 0 (the first 24 hr from birth, P0) to P30. METHODS: We used immunocytochemistry to study the presence of intracallosal NK1‐immunopositive neurons (NK1(IP) (‐n)...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5474716/ https://www.ncbi.nlm.nih.gov/pubmed/28638718 http://dx.doi.org/10.1002/brb3.713 |
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author | Barbaresi, Paolo Mensà, Emanuela Bastioli, Guendalina Amoroso, Salvatore |
author_facet | Barbaresi, Paolo Mensà, Emanuela Bastioli, Guendalina Amoroso, Salvatore |
author_sort | Barbaresi, Paolo |
collection | PubMed |
description | INTRODUCTION: The expression of substance P (SP) receptor (neurokinin 1, NK1) was studied in the rat corpus callosum (cc) from postnatal day 0 (the first 24 hr from birth, P0) to P30. METHODS: We used immunocytochemistry to study the presence of intracallosal NK1‐immunopositive neurons (NK1(IP) (‐n)) during cc development. RESULTS: NK1(IP) (‐n) first appeared on P5. Their number increased significantly between P5 and P10, it remained almost constant between P10 and P15, then declined slightly until P30. The size of intracallosal NK1(IP) (‐n) increased constantly from P5 (102.3 μm(2)) to P30 (262.07 μm(2)). From P5 onward, their distribution pattern was adult‐like, that is, they were more numerous in the lateral and intermediate parts of the cc, and declined to few or none approaching the midline. At P5, intracallosal NK1(IP) (‐n) had a predominantly round cell bodies with primary dendrites of different thickness from which originated thinner secondary branches. Between P10 and P15, dendrites were longer and more thickly branched, and displayed several varicosities as well as short, thin appendages. Between P20 and P30, NK1(IP) (‐n) were qualitatively indistinguishable from those of adult animals and could be classified as bipolar (fusiform and rectangular), round–polygonal, and pyramidal (triangular–pyriform). CONCLUSIONS: Number of NK1(IP) (‐n) increase between P5 and P10, then declines, but unlike other intracallosal neurons, NK1(IP) (‐n) make up a significant population in the adult cc. These findings suggest that NK1(IP) (‐n) may be involved in the myelination of callosal axons, could play an important role in their pathfinding. Since they are also found in adult rat cc, it is likely that their role changes during lifetime. |
format | Online Article Text |
id | pubmed-5474716 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-54747162017-06-21 Substance P NK1 receptor in the rat corpus callosum during postnatal development Barbaresi, Paolo Mensà, Emanuela Bastioli, Guendalina Amoroso, Salvatore Brain Behav Original Research INTRODUCTION: The expression of substance P (SP) receptor (neurokinin 1, NK1) was studied in the rat corpus callosum (cc) from postnatal day 0 (the first 24 hr from birth, P0) to P30. METHODS: We used immunocytochemistry to study the presence of intracallosal NK1‐immunopositive neurons (NK1(IP) (‐n)) during cc development. RESULTS: NK1(IP) (‐n) first appeared on P5. Their number increased significantly between P5 and P10, it remained almost constant between P10 and P15, then declined slightly until P30. The size of intracallosal NK1(IP) (‐n) increased constantly from P5 (102.3 μm(2)) to P30 (262.07 μm(2)). From P5 onward, their distribution pattern was adult‐like, that is, they were more numerous in the lateral and intermediate parts of the cc, and declined to few or none approaching the midline. At P5, intracallosal NK1(IP) (‐n) had a predominantly round cell bodies with primary dendrites of different thickness from which originated thinner secondary branches. Between P10 and P15, dendrites were longer and more thickly branched, and displayed several varicosities as well as short, thin appendages. Between P20 and P30, NK1(IP) (‐n) were qualitatively indistinguishable from those of adult animals and could be classified as bipolar (fusiform and rectangular), round–polygonal, and pyramidal (triangular–pyriform). CONCLUSIONS: Number of NK1(IP) (‐n) increase between P5 and P10, then declines, but unlike other intracallosal neurons, NK1(IP) (‐n) make up a significant population in the adult cc. These findings suggest that NK1(IP) (‐n) may be involved in the myelination of callosal axons, could play an important role in their pathfinding. Since they are also found in adult rat cc, it is likely that their role changes during lifetime. John Wiley and Sons Inc. 2017-05-02 /pmc/articles/PMC5474716/ /pubmed/28638718 http://dx.doi.org/10.1002/brb3.713 Text en © 2017 The Authors. Brain and Behavior published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Barbaresi, Paolo Mensà, Emanuela Bastioli, Guendalina Amoroso, Salvatore Substance P NK1 receptor in the rat corpus callosum during postnatal development |
title | Substance P NK1 receptor in the rat corpus callosum during postnatal development |
title_full | Substance P NK1 receptor in the rat corpus callosum during postnatal development |
title_fullStr | Substance P NK1 receptor in the rat corpus callosum during postnatal development |
title_full_unstemmed | Substance P NK1 receptor in the rat corpus callosum during postnatal development |
title_short | Substance P NK1 receptor in the rat corpus callosum during postnatal development |
title_sort | substance p nk1 receptor in the rat corpus callosum during postnatal development |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5474716/ https://www.ncbi.nlm.nih.gov/pubmed/28638718 http://dx.doi.org/10.1002/brb3.713 |
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