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Afferent neurons of the kidney with impaired firing pattern in inflammation – role of sodium currents?

Peripheral neurons with renal afferents exhibit a predominantly tonic firing pattern of higher frequency that is reduced to low frequencies (phasic firing pattern) in renal inflammation. We wanted to test the hypothesis that the reduction in firing activity during inflammation is due to high-activit...

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Autores principales: Lale, Nena, Ditting, Tilmann, Hilgers, Karl F., Linz, Peter, Ott, Christian, Schmieder, Roland E., Schiffer, Mario, Amann, Kerstin, Veelken, Roland, Rodionova, Kristina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10567872/
https://www.ncbi.nlm.nih.gov/pubmed/37672108
http://dx.doi.org/10.1007/s00424-023-02852-6
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author Lale, Nena
Ditting, Tilmann
Hilgers, Karl F.
Linz, Peter
Ott, Christian
Schmieder, Roland E.
Schiffer, Mario
Amann, Kerstin
Veelken, Roland
Rodionova, Kristina
author_facet Lale, Nena
Ditting, Tilmann
Hilgers, Karl F.
Linz, Peter
Ott, Christian
Schmieder, Roland E.
Schiffer, Mario
Amann, Kerstin
Veelken, Roland
Rodionova, Kristina
author_sort Lale, Nena
collection PubMed
description Peripheral neurons with renal afferents exhibit a predominantly tonic firing pattern of higher frequency that is reduced to low frequencies (phasic firing pattern) in renal inflammation. We wanted to test the hypothesis that the reduction in firing activity during inflammation is due to high-activity tonic neurons switching from higher to low frequencies depending on altered sodium currents. We identified and cultivated afferent sensory neurons with renal projections from the dorsal root ganglia (Th11-L2). Cultivated neurons were incubated with the chemokine CXCL1 (1,5 nmol/ml) for 12 h. We characterized neurons as “tonic,” i.e., sustained action potential (AP) firing, or “phasic,” i.e., < 5 APs upon stimulation in the current clamp. Their membrane currents were investigated in a voltage clamp. Data analyzed: renal vs. non-renal and tonic vs. phasic neurons. Renal afferent neurons exposed to CXCL1 showed a decrease in tonic firing pattern (CXCL1: 35,6% vs. control: 57%, P < 0.05). Na(+) and K(+) currents were not different between control renal and non-renal DRG neurons. Phasic neurons exhibited higher Na(+) and K(+) currents than tonic resulting in shorter APs (3.7 ± 0.3 vs. 6.1 ± 0.6 ms, P < 0.01). In neurons incubated with CXCL1, Na(+) and K(+) peak current density increased in phasic (Na(+): − 969 ± 47 vs. − 758 ± 47 nA/pF, P < 0.01; K(+): 707 ± 22 vs. 558 ± 31 nA/pF, P < 0.01), but were unchanged in tonic neurons. Phasic neurons exposed to CXCL1 showed a broader range of Na(+) currents ([− 365– − 1429 nA] vs. [− 412– − 4273 nA]; P < 0.05) similar to tonic neurons. After CXCL1 exposure, significant changes in phasic neurons were observed in sodium activation/inactivation as well as a wider distribution of Na(+) currents characteristic of tonic neurons. These findings indicate a subgroup of tonic neurons besides mere tonic or phasic neurons exists able to exhibit a phasic activity pattern under pathological conditions.
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spelling pubmed-105678722023-10-13 Afferent neurons of the kidney with impaired firing pattern in inflammation – role of sodium currents? Lale, Nena Ditting, Tilmann Hilgers, Karl F. Linz, Peter Ott, Christian Schmieder, Roland E. Schiffer, Mario Amann, Kerstin Veelken, Roland Rodionova, Kristina Pflugers Arch Sensory Physiology Peripheral neurons with renal afferents exhibit a predominantly tonic firing pattern of higher frequency that is reduced to low frequencies (phasic firing pattern) in renal inflammation. We wanted to test the hypothesis that the reduction in firing activity during inflammation is due to high-activity tonic neurons switching from higher to low frequencies depending on altered sodium currents. We identified and cultivated afferent sensory neurons with renal projections from the dorsal root ganglia (Th11-L2). Cultivated neurons were incubated with the chemokine CXCL1 (1,5 nmol/ml) for 12 h. We characterized neurons as “tonic,” i.e., sustained action potential (AP) firing, or “phasic,” i.e., < 5 APs upon stimulation in the current clamp. Their membrane currents were investigated in a voltage clamp. Data analyzed: renal vs. non-renal and tonic vs. phasic neurons. Renal afferent neurons exposed to CXCL1 showed a decrease in tonic firing pattern (CXCL1: 35,6% vs. control: 57%, P < 0.05). Na(+) and K(+) currents were not different between control renal and non-renal DRG neurons. Phasic neurons exhibited higher Na(+) and K(+) currents than tonic resulting in shorter APs (3.7 ± 0.3 vs. 6.1 ± 0.6 ms, P < 0.01). In neurons incubated with CXCL1, Na(+) and K(+) peak current density increased in phasic (Na(+): − 969 ± 47 vs. − 758 ± 47 nA/pF, P < 0.01; K(+): 707 ± 22 vs. 558 ± 31 nA/pF, P < 0.01), but were unchanged in tonic neurons. Phasic neurons exposed to CXCL1 showed a broader range of Na(+) currents ([− 365– − 1429 nA] vs. [− 412– − 4273 nA]; P < 0.05) similar to tonic neurons. After CXCL1 exposure, significant changes in phasic neurons were observed in sodium activation/inactivation as well as a wider distribution of Na(+) currents characteristic of tonic neurons. These findings indicate a subgroup of tonic neurons besides mere tonic or phasic neurons exists able to exhibit a phasic activity pattern under pathological conditions. Springer Berlin Heidelberg 2023-09-06 2023 /pmc/articles/PMC10567872/ /pubmed/37672108 http://dx.doi.org/10.1007/s00424-023-02852-6 Text en © The Author(s) 2023 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Sensory Physiology
Lale, Nena
Ditting, Tilmann
Hilgers, Karl F.
Linz, Peter
Ott, Christian
Schmieder, Roland E.
Schiffer, Mario
Amann, Kerstin
Veelken, Roland
Rodionova, Kristina
Afferent neurons of the kidney with impaired firing pattern in inflammation – role of sodium currents?
title Afferent neurons of the kidney with impaired firing pattern in inflammation – role of sodium currents?
title_full Afferent neurons of the kidney with impaired firing pattern in inflammation – role of sodium currents?
title_fullStr Afferent neurons of the kidney with impaired firing pattern in inflammation – role of sodium currents?
title_full_unstemmed Afferent neurons of the kidney with impaired firing pattern in inflammation – role of sodium currents?
title_short Afferent neurons of the kidney with impaired firing pattern in inflammation – role of sodium currents?
title_sort afferent neurons of the kidney with impaired firing pattern in inflammation – role of sodium currents?
topic Sensory Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10567872/
https://www.ncbi.nlm.nih.gov/pubmed/37672108
http://dx.doi.org/10.1007/s00424-023-02852-6
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