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Analysis of the distribution of vagal afferent projections from different peripheral organs to the nucleus of the solitary tract in rats
Anatomical tracing studies examining the vagal system can conflate details of sensory afferent and motor efferent neurons. Here, we used a serotype of adeno‐associated virus that transports retrogradely and exhibits selective tropism for vagal afferents, to map their soma location and central termin...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9804483/ https://www.ncbi.nlm.nih.gov/pubmed/35988033 http://dx.doi.org/10.1002/cne.25398 |
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author | Bassi, Jaspreet K. Connelly, Angela A. Butler, Andrew G. Liu, Yehe Ghanbari, Anahita Farmer, David G. S. Jenkins, Michael W. Melo, Mariana R. McDougall, Stuart J. Allen, Andrew M. |
author_facet | Bassi, Jaspreet K. Connelly, Angela A. Butler, Andrew G. Liu, Yehe Ghanbari, Anahita Farmer, David G. S. Jenkins, Michael W. Melo, Mariana R. McDougall, Stuart J. Allen, Andrew M. |
author_sort | Bassi, Jaspreet K. |
collection | PubMed |
description | Anatomical tracing studies examining the vagal system can conflate details of sensory afferent and motor efferent neurons. Here, we used a serotype of adeno‐associated virus that transports retrogradely and exhibits selective tropism for vagal afferents, to map their soma location and central termination sites within the nucleus of the solitary tract (NTS). We examined the vagal sensory afferents innervating the trachea, duodenum, stomach, or heart, and in some animals, from two organs concurrently. We observed no obvious somatotopy in the somata distribution within the nodose ganglion. The central termination patterns of afferents from different organs within the NTS overlap substantially. Convergence of vagal afferent inputs from different organs onto single NTS neurons is observed. Abdominal and thoracic afferents terminate throughout the NTS, including in the rostral NTS, where the 7th cranial nerve inputs are known to synapse. To address whether the axonal labeling produced by viral transduction is so widespread because it fills axons traveling to their targets, and not just terminal fields, we labeled pre and postsynaptic elements of vagal afferents in the NTS . Vagal afferents form multiple putative synapses as they course through the NTS, with each vagal afferent neuron distributing sensory signals to multiple second‐order NTS neurons. We observe little selectivity between vagal afferents from different visceral targets and NTS neurons with common neurochemical phenotypes, with afferents from different organs making close appositions with the same NTS neuron. We conclude that specific viscerosensory information is distributed widely within the NTS and that the coding of this input is probably determined by the intrinsic properties and projections of the second‐order neuron. |
format | Online Article Text |
id | pubmed-9804483 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98044832023-01-03 Analysis of the distribution of vagal afferent projections from different peripheral organs to the nucleus of the solitary tract in rats Bassi, Jaspreet K. Connelly, Angela A. Butler, Andrew G. Liu, Yehe Ghanbari, Anahita Farmer, David G. S. Jenkins, Michael W. Melo, Mariana R. McDougall, Stuart J. Allen, Andrew M. J Comp Neurol Research Articles Anatomical tracing studies examining the vagal system can conflate details of sensory afferent and motor efferent neurons. Here, we used a serotype of adeno‐associated virus that transports retrogradely and exhibits selective tropism for vagal afferents, to map their soma location and central termination sites within the nucleus of the solitary tract (NTS). We examined the vagal sensory afferents innervating the trachea, duodenum, stomach, or heart, and in some animals, from two organs concurrently. We observed no obvious somatotopy in the somata distribution within the nodose ganglion. The central termination patterns of afferents from different organs within the NTS overlap substantially. Convergence of vagal afferent inputs from different organs onto single NTS neurons is observed. Abdominal and thoracic afferents terminate throughout the NTS, including in the rostral NTS, where the 7th cranial nerve inputs are known to synapse. To address whether the axonal labeling produced by viral transduction is so widespread because it fills axons traveling to their targets, and not just terminal fields, we labeled pre and postsynaptic elements of vagal afferents in the NTS . Vagal afferents form multiple putative synapses as they course through the NTS, with each vagal afferent neuron distributing sensory signals to multiple second‐order NTS neurons. We observe little selectivity between vagal afferents from different visceral targets and NTS neurons with common neurochemical phenotypes, with afferents from different organs making close appositions with the same NTS neuron. We conclude that specific viscerosensory information is distributed widely within the NTS and that the coding of this input is probably determined by the intrinsic properties and projections of the second‐order neuron. John Wiley and Sons Inc. 2022-08-21 2022-12 /pmc/articles/PMC9804483/ /pubmed/35988033 http://dx.doi.org/10.1002/cne.25398 Text en © 2022 The Authors. The Journal of Comparative Neurology published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Articles Bassi, Jaspreet K. Connelly, Angela A. Butler, Andrew G. Liu, Yehe Ghanbari, Anahita Farmer, David G. S. Jenkins, Michael W. Melo, Mariana R. McDougall, Stuart J. Allen, Andrew M. Analysis of the distribution of vagal afferent projections from different peripheral organs to the nucleus of the solitary tract in rats |
title | Analysis of the distribution of vagal afferent projections from different peripheral organs to the nucleus of the solitary tract in rats |
title_full | Analysis of the distribution of vagal afferent projections from different peripheral organs to the nucleus of the solitary tract in rats |
title_fullStr | Analysis of the distribution of vagal afferent projections from different peripheral organs to the nucleus of the solitary tract in rats |
title_full_unstemmed | Analysis of the distribution of vagal afferent projections from different peripheral organs to the nucleus of the solitary tract in rats |
title_short | Analysis of the distribution of vagal afferent projections from different peripheral organs to the nucleus of the solitary tract in rats |
title_sort | analysis of the distribution of vagal afferent projections from different peripheral organs to the nucleus of the solitary tract in rats |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9804483/ https://www.ncbi.nlm.nih.gov/pubmed/35988033 http://dx.doi.org/10.1002/cne.25398 |
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