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Quantitative Study of NPY-Expressing GABAergic Neurons and Axons in Rat Spinal Dorsal Horn*
Between 25–40% of neurons in laminae I–III are GABAergic, and some of these express neuropeptide Y (NPY). We previously reported that NPY-immunoreactive axons form numerous synapses on lamina III projection neurons that possess the neurokinin 1 receptor (NK1r). The aims of this study were to determi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wiley Subscription Services, Inc., A Wiley Company
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3258544/ https://www.ncbi.nlm.nih.gov/pubmed/21344400 http://dx.doi.org/10.1002/cne.22570 |
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author | Polgár, Erika Sardella, Thomas CP Watanabe, Masahiko Todd, Andrew J |
author_facet | Polgár, Erika Sardella, Thomas CP Watanabe, Masahiko Todd, Andrew J |
author_sort | Polgár, Erika |
collection | PubMed |
description | Between 25–40% of neurons in laminae I–III are GABAergic, and some of these express neuropeptide Y (NPY). We previously reported that NPY-immunoreactive axons form numerous synapses on lamina III projection neurons that possess the neurokinin 1 receptor (NK1r). The aims of this study were to determine the proportion of neurons and GABAergic boutons in this region that contain NPY, and to look for evidence that they selectively innervate different neuronal populations. We found that 4–6% of neurons in laminae I–III were NPY-immunoreactive and based on the proportions of neurons that are GABAergic, we estimate that NPY is expressed by 18% of inhibitory interneurons in laminae I–II and 9% of those in lamina III. GABAergic boutons were identified by the presence of the vesicular GABA transporter (VGAT) and NPY was found in 13–15% of VGAT-immunoreactive boutons in laminae I–II, and 5% of those in lamina III. For both the lamina III NK1r-immunoreactive projection neurons and protein kinase Cγ (PKCγ)-immunoreactive interneurons in lamina II, we found that around one-third of the VGAT boutons that contacted them were NPY-immunoreactive. However, based on differences in the sizes of these boutons and the strength of their NPY-immunoreactivity, we conclude that these originate from different populations of interneurons. Only 6% of VGAT boutons presynaptic to large lamina I projection neurons that lacked NK1rs contained NPY. These results show that NPY-containing neurons make up a considerable proportion of the inhibitory interneurons in laminae I–III, and that their axons preferentially target certain classes of dorsal horn neuron. J. Comp. Neurol. 519:1007–1023, 2011. © 2010 Wiley-Liss, Inc. |
format | Online Article Text |
id | pubmed-3258544 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Wiley Subscription Services, Inc., A Wiley Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-32585442012-01-17 Quantitative Study of NPY-Expressing GABAergic Neurons and Axons in Rat Spinal Dorsal Horn* Polgár, Erika Sardella, Thomas CP Watanabe, Masahiko Todd, Andrew J J Comp Neurol Research Article Between 25–40% of neurons in laminae I–III are GABAergic, and some of these express neuropeptide Y (NPY). We previously reported that NPY-immunoreactive axons form numerous synapses on lamina III projection neurons that possess the neurokinin 1 receptor (NK1r). The aims of this study were to determine the proportion of neurons and GABAergic boutons in this region that contain NPY, and to look for evidence that they selectively innervate different neuronal populations. We found that 4–6% of neurons in laminae I–III were NPY-immunoreactive and based on the proportions of neurons that are GABAergic, we estimate that NPY is expressed by 18% of inhibitory interneurons in laminae I–II and 9% of those in lamina III. GABAergic boutons were identified by the presence of the vesicular GABA transporter (VGAT) and NPY was found in 13–15% of VGAT-immunoreactive boutons in laminae I–II, and 5% of those in lamina III. For both the lamina III NK1r-immunoreactive projection neurons and protein kinase Cγ (PKCγ)-immunoreactive interneurons in lamina II, we found that around one-third of the VGAT boutons that contacted them were NPY-immunoreactive. However, based on differences in the sizes of these boutons and the strength of their NPY-immunoreactivity, we conclude that these originate from different populations of interneurons. Only 6% of VGAT boutons presynaptic to large lamina I projection neurons that lacked NK1rs contained NPY. These results show that NPY-containing neurons make up a considerable proportion of the inhibitory interneurons in laminae I–III, and that their axons preferentially target certain classes of dorsal horn neuron. J. Comp. Neurol. 519:1007–1023, 2011. © 2010 Wiley-Liss, Inc. Wiley Subscription Services, Inc., A Wiley Company 2011-04-15 2010-12-23 /pmc/articles/PMC3258544/ /pubmed/21344400 http://dx.doi.org/10.1002/cne.22570 Text en Copyright © 2011 Wiley-Liss, Inc., A Wiley Company http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation. |
spellingShingle | Research Article Polgár, Erika Sardella, Thomas CP Watanabe, Masahiko Todd, Andrew J Quantitative Study of NPY-Expressing GABAergic Neurons and Axons in Rat Spinal Dorsal Horn* |
title | Quantitative Study of NPY-Expressing GABAergic Neurons and Axons in Rat Spinal Dorsal Horn* |
title_full | Quantitative Study of NPY-Expressing GABAergic Neurons and Axons in Rat Spinal Dorsal Horn* |
title_fullStr | Quantitative Study of NPY-Expressing GABAergic Neurons and Axons in Rat Spinal Dorsal Horn* |
title_full_unstemmed | Quantitative Study of NPY-Expressing GABAergic Neurons and Axons in Rat Spinal Dorsal Horn* |
title_short | Quantitative Study of NPY-Expressing GABAergic Neurons and Axons in Rat Spinal Dorsal Horn* |
title_sort | quantitative study of npy-expressing gabaergic neurons and axons in rat spinal dorsal horn* |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3258544/ https://www.ncbi.nlm.nih.gov/pubmed/21344400 http://dx.doi.org/10.1002/cne.22570 |
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