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A brainstem map for visceral sensations
The nervous system uses various coding strategies to process sensory inputs. For example, the olfactory system uses large receptor repertoires and is wired to recognize diverse odours, whereas the visual system provides high acuity of object position, form and movement(1–5). Compared to external sen...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9452305/ https://www.ncbi.nlm.nih.gov/pubmed/36045291 http://dx.doi.org/10.1038/s41586-022-05139-5 |
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author | Ran, Chen Boettcher, Jack C. Kaye, Judith A. Gallori, Catherine E. Liberles, Stephen D. |
author_facet | Ran, Chen Boettcher, Jack C. Kaye, Judith A. Gallori, Catherine E. Liberles, Stephen D. |
author_sort | Ran, Chen |
collection | PubMed |
description | The nervous system uses various coding strategies to process sensory inputs. For example, the olfactory system uses large receptor repertoires and is wired to recognize diverse odours, whereas the visual system provides high acuity of object position, form and movement(1–5). Compared to external sensory systems, principles that underlie sensory processing by the interoceptive nervous system remain poorly defined. Here we developed a two-photon calcium imaging preparation to understand internal organ representations in the nucleus of the solitary tract (NTS), a sensory gateway in the brainstem that receives vagal and other inputs from the body. Focusing on gut and upper airway stimuli, we observed that individual NTS neurons are tuned to detect signals from particular organs and are topographically organized on the basis of body position. Moreover, some mechanosensory and chemosensory inputs from the same organ converge centrally. Sensory inputs engage specific NTS domains with defined locations, each containing heterogeneous cell types. Spatial representations of different organs are further sharpened in the NTS beyond what is achieved by vagal axon sorting alone, as blockade of brainstem inhibition broadens neural tuning and disorganizes visceral representations. These findings reveal basic organizational features used by the brain to process interoceptive inputs. |
format | Online Article Text |
id | pubmed-9452305 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-94523052022-09-09 A brainstem map for visceral sensations Ran, Chen Boettcher, Jack C. Kaye, Judith A. Gallori, Catherine E. Liberles, Stephen D. Nature Article The nervous system uses various coding strategies to process sensory inputs. For example, the olfactory system uses large receptor repertoires and is wired to recognize diverse odours, whereas the visual system provides high acuity of object position, form and movement(1–5). Compared to external sensory systems, principles that underlie sensory processing by the interoceptive nervous system remain poorly defined. Here we developed a two-photon calcium imaging preparation to understand internal organ representations in the nucleus of the solitary tract (NTS), a sensory gateway in the brainstem that receives vagal and other inputs from the body. Focusing on gut and upper airway stimuli, we observed that individual NTS neurons are tuned to detect signals from particular organs and are topographically organized on the basis of body position. Moreover, some mechanosensory and chemosensory inputs from the same organ converge centrally. Sensory inputs engage specific NTS domains with defined locations, each containing heterogeneous cell types. Spatial representations of different organs are further sharpened in the NTS beyond what is achieved by vagal axon sorting alone, as blockade of brainstem inhibition broadens neural tuning and disorganizes visceral representations. These findings reveal basic organizational features used by the brain to process interoceptive inputs. Nature Publishing Group UK 2022-08-31 2022 /pmc/articles/PMC9452305/ /pubmed/36045291 http://dx.doi.org/10.1038/s41586-022-05139-5 Text en © The Author(s) 2022, corrected publication 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Ran, Chen Boettcher, Jack C. Kaye, Judith A. Gallori, Catherine E. Liberles, Stephen D. A brainstem map for visceral sensations |
title | A brainstem map for visceral sensations |
title_full | A brainstem map for visceral sensations |
title_fullStr | A brainstem map for visceral sensations |
title_full_unstemmed | A brainstem map for visceral sensations |
title_short | A brainstem map for visceral sensations |
title_sort | brainstem map for visceral sensations |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9452305/ https://www.ncbi.nlm.nih.gov/pubmed/36045291 http://dx.doi.org/10.1038/s41586-022-05139-5 |
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