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Kv3 Channels Contribute to the Excitability of Subpopulations of Spinal Cord Neurons in Lamina VII
Autonomic parasympathetic preganglionic neurons (PGNs) drive contraction of the bladder during micturition but remain quiescent during bladder filling. This quiescence is postulated to be because of recurrent inhibition of PGN by fast-firing adjoining interneurons. Here, we defined four distinct neu...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Society for Neuroscience
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8868027/ https://www.ncbi.nlm.nih.gov/pubmed/35058310 http://dx.doi.org/10.1523/ENEURO.0510-21.2021 |
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author | Mullen, Pierce N. Pilati, Nadia Large, Charles H. Deuchars, Jim Deuchars, Susan A. |
author_facet | Mullen, Pierce N. Pilati, Nadia Large, Charles H. Deuchars, Jim Deuchars, Susan A. |
author_sort | Mullen, Pierce N. |
collection | PubMed |
description | Autonomic parasympathetic preganglionic neurons (PGNs) drive contraction of the bladder during micturition but remain quiescent during bladder filling. This quiescence is postulated to be because of recurrent inhibition of PGN by fast-firing adjoining interneurons. Here, we defined four distinct neuronal types within Lamina VII, where PGN are situated, by combining whole cell patch clamp recordings with k-means clustering of a range of electrophysiological parameters. Additional morphologic analysis separated these neuronal classes into parasympathetic preganglionic populations (PGN) and a fast-firing interneuronal population. Kv3 channels are voltage-gated potassium channels (Kv) that allow fast and precise firing of neurons. We found that blockade of Kv3 channels by tetraethylammonium (TEA) reduced neuronal firing frequency and isolated high-voltage-activated Kv currents in the fast-firing population but had no effect in PGN populations. Furthermore, Kv3 blockade potentiated the local and descending inhibitory inputs to PGN indicating that Kv3-expressing inhibitory neurons are synaptically connected to PGN. Taken together, our data reveal that Kv3 channels are crucial for fast and regulated neuronal output of a defined population that may be involved in intrinsic spinal bladder circuits that underpin recurrent inhibition of PGN. |
format | Online Article Text |
id | pubmed-8868027 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Society for Neuroscience |
record_format | MEDLINE/PubMed |
spelling | pubmed-88680272022-02-25 Kv3 Channels Contribute to the Excitability of Subpopulations of Spinal Cord Neurons in Lamina VII Mullen, Pierce N. Pilati, Nadia Large, Charles H. Deuchars, Jim Deuchars, Susan A. eNeuro Research Article: New Research Autonomic parasympathetic preganglionic neurons (PGNs) drive contraction of the bladder during micturition but remain quiescent during bladder filling. This quiescence is postulated to be because of recurrent inhibition of PGN by fast-firing adjoining interneurons. Here, we defined four distinct neuronal types within Lamina VII, where PGN are situated, by combining whole cell patch clamp recordings with k-means clustering of a range of electrophysiological parameters. Additional morphologic analysis separated these neuronal classes into parasympathetic preganglionic populations (PGN) and a fast-firing interneuronal population. Kv3 channels are voltage-gated potassium channels (Kv) that allow fast and precise firing of neurons. We found that blockade of Kv3 channels by tetraethylammonium (TEA) reduced neuronal firing frequency and isolated high-voltage-activated Kv currents in the fast-firing population but had no effect in PGN populations. Furthermore, Kv3 blockade potentiated the local and descending inhibitory inputs to PGN indicating that Kv3-expressing inhibitory neurons are synaptically connected to PGN. Taken together, our data reveal that Kv3 channels are crucial for fast and regulated neuronal output of a defined population that may be involved in intrinsic spinal bladder circuits that underpin recurrent inhibition of PGN. Society for Neuroscience 2022-02-17 /pmc/articles/PMC8868027/ /pubmed/35058310 http://dx.doi.org/10.1523/ENEURO.0510-21.2021 Text en Copyright © 2022 Mullen et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Research Article: New Research Mullen, Pierce N. Pilati, Nadia Large, Charles H. Deuchars, Jim Deuchars, Susan A. Kv3 Channels Contribute to the Excitability of Subpopulations of Spinal Cord Neurons in Lamina VII |
title | Kv3 Channels Contribute to the Excitability of Subpopulations of Spinal Cord Neurons in Lamina VII |
title_full | Kv3 Channels Contribute to the Excitability of Subpopulations of Spinal Cord Neurons in Lamina VII |
title_fullStr | Kv3 Channels Contribute to the Excitability of Subpopulations of Spinal Cord Neurons in Lamina VII |
title_full_unstemmed | Kv3 Channels Contribute to the Excitability of Subpopulations of Spinal Cord Neurons in Lamina VII |
title_short | Kv3 Channels Contribute to the Excitability of Subpopulations of Spinal Cord Neurons in Lamina VII |
title_sort | kv3 channels contribute to the excitability of subpopulations of spinal cord neurons in lamina vii |
topic | Research Article: New Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8868027/ https://www.ncbi.nlm.nih.gov/pubmed/35058310 http://dx.doi.org/10.1523/ENEURO.0510-21.2021 |
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