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Spinoparabrachial projection neurons form distinct classes in the mouse dorsal horn

Projection neurons in the spinal dorsal horn relay sensory information to higher brain centres. The activation of these populations is shaped by afferent input from the periphery, descending input from the brain, and input from local interneuron circuits. Much of our recent understanding of dorsal h...

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Autores principales: Browne, Tyler J., Smith, Kelly M., Gradwell, Mark A., Iredale, Jacqueline A., Dayas, Christopher V., Callister, Robert J., Hughes, David I., Graham, Brett A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8208100/
https://www.ncbi.nlm.nih.gov/pubmed/33779126
http://dx.doi.org/10.1097/j.pain.0000000000002194
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author Browne, Tyler J.
Smith, Kelly M.
Gradwell, Mark A.
Iredale, Jacqueline A.
Dayas, Christopher V.
Callister, Robert J.
Hughes, David I.
Graham, Brett A.
author_facet Browne, Tyler J.
Smith, Kelly M.
Gradwell, Mark A.
Iredale, Jacqueline A.
Dayas, Christopher V.
Callister, Robert J.
Hughes, David I.
Graham, Brett A.
author_sort Browne, Tyler J.
collection PubMed
description Projection neurons in the spinal dorsal horn relay sensory information to higher brain centres. The activation of these populations is shaped by afferent input from the periphery, descending input from the brain, and input from local interneuron circuits. Much of our recent understanding of dorsal horn circuitry comes from studies in transgenic mice; however, information on projection neurons is still based largely on studies in monkey, cat, and rat. We used viral labelling to identify and record from mouse parabrachial nucleus (PBN) projecting neurons located in the dorsal horn of spinal cord slices. Overall, mouse lamina I spinoparabrachial projection neurons (SPBNs) exhibit many electrophysiological and morphological features that overlap with rat. Unbiased cluster analysis distinguished 4 distinct subpopulations of lamina I SPBNs, based on their electrophysiological properties that may underlie different sensory signalling features in each group. We also provide novel information on SPBNs in the deeper lamina (III-V), which have not been previously studied by patch clamp analysis. These neurons exhibited higher action potential discharge frequencies and received weaker excitatory synaptic input than lamina I SPBNs, suggesting this deeper population produces different sensory codes destined for the PBN. Mouse SPBNs from both regions (laminae I and III-V) were often seen to give off local axon collaterals, and we provide neuroanatomical evidence they contribute to excitatory input to dorsal horn circuits. These data provide novel information to implicate excitatory input from parabrachial projection neuron in dorsal horn circuit activity during processing of nociceptive information, as well as defining deep dorsal horn projection neurons that provide an alternative route by which sensory information can reach the PBN.
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spelling pubmed-82081002021-06-16 Spinoparabrachial projection neurons form distinct classes in the mouse dorsal horn Browne, Tyler J. Smith, Kelly M. Gradwell, Mark A. Iredale, Jacqueline A. Dayas, Christopher V. Callister, Robert J. Hughes, David I. Graham, Brett A. Pain Research Paper Projection neurons in the spinal dorsal horn relay sensory information to higher brain centres. The activation of these populations is shaped by afferent input from the periphery, descending input from the brain, and input from local interneuron circuits. Much of our recent understanding of dorsal horn circuitry comes from studies in transgenic mice; however, information on projection neurons is still based largely on studies in monkey, cat, and rat. We used viral labelling to identify and record from mouse parabrachial nucleus (PBN) projecting neurons located in the dorsal horn of spinal cord slices. Overall, mouse lamina I spinoparabrachial projection neurons (SPBNs) exhibit many electrophysiological and morphological features that overlap with rat. Unbiased cluster analysis distinguished 4 distinct subpopulations of lamina I SPBNs, based on their electrophysiological properties that may underlie different sensory signalling features in each group. We also provide novel information on SPBNs in the deeper lamina (III-V), which have not been previously studied by patch clamp analysis. These neurons exhibited higher action potential discharge frequencies and received weaker excitatory synaptic input than lamina I SPBNs, suggesting this deeper population produces different sensory codes destined for the PBN. Mouse SPBNs from both regions (laminae I and III-V) were often seen to give off local axon collaterals, and we provide neuroanatomical evidence they contribute to excitatory input to dorsal horn circuits. These data provide novel information to implicate excitatory input from parabrachial projection neuron in dorsal horn circuit activity during processing of nociceptive information, as well as defining deep dorsal horn projection neurons that provide an alternative route by which sensory information can reach the PBN. Wolters Kluwer 2021-07 2021-02-22 /pmc/articles/PMC8208100/ /pubmed/33779126 http://dx.doi.org/10.1097/j.pain.0000000000002194 Text en Copyright © 2021 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the International Association for the Study of Pain. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY) (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Browne, Tyler J.
Smith, Kelly M.
Gradwell, Mark A.
Iredale, Jacqueline A.
Dayas, Christopher V.
Callister, Robert J.
Hughes, David I.
Graham, Brett A.
Spinoparabrachial projection neurons form distinct classes in the mouse dorsal horn
title Spinoparabrachial projection neurons form distinct classes in the mouse dorsal horn
title_full Spinoparabrachial projection neurons form distinct classes in the mouse dorsal horn
title_fullStr Spinoparabrachial projection neurons form distinct classes in the mouse dorsal horn
title_full_unstemmed Spinoparabrachial projection neurons form distinct classes in the mouse dorsal horn
title_short Spinoparabrachial projection neurons form distinct classes in the mouse dorsal horn
title_sort spinoparabrachial projection neurons form distinct classes in the mouse dorsal horn
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8208100/
https://www.ncbi.nlm.nih.gov/pubmed/33779126
http://dx.doi.org/10.1097/j.pain.0000000000002194
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