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Novel inhibitory brainstem neurons with selective projections to spinal lamina I reduce both pain and itch
Sensory information is transmitted from peripheral nerves, through the spinal cord, and up to the brain (“bottom up” pathway). Some of this information may be modulated by “top‐down” projections from the brain to the spinal cord. Discovering endogenous mechanisms for reducing pain and itch holds eno...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8009815/ https://www.ncbi.nlm.nih.gov/pubmed/33247430 http://dx.doi.org/10.1002/cne.25076 |
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author | Agostinelli, Lindsay J. Bassuk, Alexander G. |
author_facet | Agostinelli, Lindsay J. Bassuk, Alexander G. |
author_sort | Agostinelli, Lindsay J. |
collection | PubMed |
description | Sensory information is transmitted from peripheral nerves, through the spinal cord, and up to the brain (“bottom up” pathway). Some of this information may be modulated by “top‐down” projections from the brain to the spinal cord. Discovering endogenous mechanisms for reducing pain and itch holds enormous potential for developing new treatments. However, neurons mediating the top‐down inhibition of pain are not well understood, nor has any such pathway been identified for itch sensation. Here, we identify a novel population of GABAergic neurons in the ventral brainstem, distinguished by prodynorphin expression, which we named LJA5. LJA5 neurons provide the only known inhibitory projection specifically to lamina I of the spinal cord, which contains sensory neurons that transmit pain and itch information up to the brain. Chemogenetically activating LJA5 neurons in male mice reduces capsaicin‐induced pain and histamine‐induced itch. Identifying this new pathway opens new treatment opportunities for chronic, refractory pain, and pruritis. |
format | Online Article Text |
id | pubmed-8009815 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-80098152021-04-16 Novel inhibitory brainstem neurons with selective projections to spinal lamina I reduce both pain and itch Agostinelli, Lindsay J. Bassuk, Alexander G. J Comp Neurol Research Articles Sensory information is transmitted from peripheral nerves, through the spinal cord, and up to the brain (“bottom up” pathway). Some of this information may be modulated by “top‐down” projections from the brain to the spinal cord. Discovering endogenous mechanisms for reducing pain and itch holds enormous potential for developing new treatments. However, neurons mediating the top‐down inhibition of pain are not well understood, nor has any such pathway been identified for itch sensation. Here, we identify a novel population of GABAergic neurons in the ventral brainstem, distinguished by prodynorphin expression, which we named LJA5. LJA5 neurons provide the only known inhibitory projection specifically to lamina I of the spinal cord, which contains sensory neurons that transmit pain and itch information up to the brain. Chemogenetically activating LJA5 neurons in male mice reduces capsaicin‐induced pain and histamine‐induced itch. Identifying this new pathway opens new treatment opportunities for chronic, refractory pain, and pruritis. John Wiley & Sons, Inc. 2020-12-04 2021-06 /pmc/articles/PMC8009815/ /pubmed/33247430 http://dx.doi.org/10.1002/cne.25076 Text en © 2020 The Authors. The Journal of Comparative Neurology published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Agostinelli, Lindsay J. Bassuk, Alexander G. Novel inhibitory brainstem neurons with selective projections to spinal lamina I reduce both pain and itch |
title | Novel inhibitory brainstem neurons with selective projections to spinal lamina I reduce both pain and itch |
title_full | Novel inhibitory brainstem neurons with selective projections to spinal lamina I reduce both pain and itch |
title_fullStr | Novel inhibitory brainstem neurons with selective projections to spinal lamina I reduce both pain and itch |
title_full_unstemmed | Novel inhibitory brainstem neurons with selective projections to spinal lamina I reduce both pain and itch |
title_short | Novel inhibitory brainstem neurons with selective projections to spinal lamina I reduce both pain and itch |
title_sort | novel inhibitory brainstem neurons with selective projections to spinal lamina i reduce both pain and itch |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8009815/ https://www.ncbi.nlm.nih.gov/pubmed/33247430 http://dx.doi.org/10.1002/cne.25076 |
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