Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Mullen, Pierce N., Pilati, Nadia, Large, Charles H., Deuchars, Jim, Deuchars, Susan A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2022
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
_version_ 1784656166197919744
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
work_keys_str_mv AT mullenpiercen kv3channelscontributetotheexcitabilityofsubpopulationsofspinalcordneuronsinlaminavii
AT pilatinadia kv3channelscontributetotheexcitabilityofsubpopulationsofspinalcordneuronsinlaminavii
AT largecharlesh kv3channelscontributetotheexcitabilityofsubpopulationsofspinalcordneuronsinlaminavii
AT deucharsjim kv3channelscontributetotheexcitabilityofsubpopulationsofspinalcordneuronsinlaminavii
AT deucharssusana kv3channelscontributetotheexcitabilityofsubpopulationsofspinalcordneuronsinlaminavii