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Tonic 5nM DA Stabilizes Neuronal Output by Enabling Bidirectional Activity-Dependent Regulation of the Hyperpolarization Activated Current via PKA and Calcineurin

Volume transmission results in phasic and tonic modulatory signals. The actions of tonic dopamine (DA) at type 1 DA receptors (D1Rs) are largely undefined. Here we show that tonic 5nM DA acts at D1Rs to stabilize neuronal output over minutes by enabling activity-dependent regulation of the hyperpola...

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Detalles Bibliográficos
Autores principales: Krenz, Wulf-Dieter C., Rodgers, Edmund W., Baro, Deborah J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4333293/
https://www.ncbi.nlm.nih.gov/pubmed/25692473
http://dx.doi.org/10.1371/journal.pone.0117965
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author Krenz, Wulf-Dieter C.
Rodgers, Edmund W.
Baro, Deborah J.
author_facet Krenz, Wulf-Dieter C.
Rodgers, Edmund W.
Baro, Deborah J.
author_sort Krenz, Wulf-Dieter C.
collection PubMed
description Volume transmission results in phasic and tonic modulatory signals. The actions of tonic dopamine (DA) at type 1 DA receptors (D1Rs) are largely undefined. Here we show that tonic 5nM DA acts at D1Rs to stabilize neuronal output over minutes by enabling activity-dependent regulation of the hyperpolarization activated current (I (h)). In the presence but not absence of 5nM DA, I (h) maximal conductance (G (max)) was adjusted according to changes in slow wave activity in order to maintain spike timing. Our study on the lateral pyloric neuron (LP), which undergoes rhythmic oscillations in membrane potential with depolarized plateaus, demonstrated that incremental, bi-directional changes in plateau duration produced corresponding alterations in LP I (h)G (max) when preparations were superfused with saline containing 5nM DA. However, when preparations were superfused with saline alone there was no linear correlation between LP I (h)G(max) and duty cycle. Thus, tonic nM DA modulated the capacity for activity to modulate LP I (h) G (max); this exemplifies metamodulation (modulation of modulation). Pretreatment with the Ca2+-chelator, BAPTA, or the specific PKA inhibitor, PKI, prevented all changes in LP I (h) in 5nM DA. Calcineurin inhibitors blocked activity-dependent changes enabled by DA and revealed a PKA-mediated, activity-independent enhancement of LP I (h)G (max). These data suggested that tonic 5nM DA produced two simultaneous, PKA-dependent effects: a direct increase in LP I (h) G (max) and a priming event that permitted calcineurin regulation of LP I (h). The latter produced graded reductions in LP I (h)G (max) with increasing duty cycles. We also demonstrated that this metamodulation preserved the timing of LP’s first spike when network output was perturbed with bath-applied 4AP. In sum, 5nM DA permits slow wave activity to provide feedback that maintains spike timing, suggesting that one function of low-level, tonic modulation is to stabilize specific features of a dynamic output.
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spelling pubmed-43332932015-02-24 Tonic 5nM DA Stabilizes Neuronal Output by Enabling Bidirectional Activity-Dependent Regulation of the Hyperpolarization Activated Current via PKA and Calcineurin Krenz, Wulf-Dieter C. Rodgers, Edmund W. Baro, Deborah J. PLoS One Research Article Volume transmission results in phasic and tonic modulatory signals. The actions of tonic dopamine (DA) at type 1 DA receptors (D1Rs) are largely undefined. Here we show that tonic 5nM DA acts at D1Rs to stabilize neuronal output over minutes by enabling activity-dependent regulation of the hyperpolarization activated current (I (h)). In the presence but not absence of 5nM DA, I (h) maximal conductance (G (max)) was adjusted according to changes in slow wave activity in order to maintain spike timing. Our study on the lateral pyloric neuron (LP), which undergoes rhythmic oscillations in membrane potential with depolarized plateaus, demonstrated that incremental, bi-directional changes in plateau duration produced corresponding alterations in LP I (h)G (max) when preparations were superfused with saline containing 5nM DA. However, when preparations were superfused with saline alone there was no linear correlation between LP I (h)G(max) and duty cycle. Thus, tonic nM DA modulated the capacity for activity to modulate LP I (h) G (max); this exemplifies metamodulation (modulation of modulation). Pretreatment with the Ca2+-chelator, BAPTA, or the specific PKA inhibitor, PKI, prevented all changes in LP I (h) in 5nM DA. Calcineurin inhibitors blocked activity-dependent changes enabled by DA and revealed a PKA-mediated, activity-independent enhancement of LP I (h)G (max). These data suggested that tonic 5nM DA produced two simultaneous, PKA-dependent effects: a direct increase in LP I (h) G (max) and a priming event that permitted calcineurin regulation of LP I (h). The latter produced graded reductions in LP I (h)G (max) with increasing duty cycles. We also demonstrated that this metamodulation preserved the timing of LP’s first spike when network output was perturbed with bath-applied 4AP. In sum, 5nM DA permits slow wave activity to provide feedback that maintains spike timing, suggesting that one function of low-level, tonic modulation is to stabilize specific features of a dynamic output. Public Library of Science 2015-02-18 /pmc/articles/PMC4333293/ /pubmed/25692473 http://dx.doi.org/10.1371/journal.pone.0117965 Text en © 2015 Krenz et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Krenz, Wulf-Dieter C.
Rodgers, Edmund W.
Baro, Deborah J.
Tonic 5nM DA Stabilizes Neuronal Output by Enabling Bidirectional Activity-Dependent Regulation of the Hyperpolarization Activated Current via PKA and Calcineurin
title Tonic 5nM DA Stabilizes Neuronal Output by Enabling Bidirectional Activity-Dependent Regulation of the Hyperpolarization Activated Current via PKA and Calcineurin
title_full Tonic 5nM DA Stabilizes Neuronal Output by Enabling Bidirectional Activity-Dependent Regulation of the Hyperpolarization Activated Current via PKA and Calcineurin
title_fullStr Tonic 5nM DA Stabilizes Neuronal Output by Enabling Bidirectional Activity-Dependent Regulation of the Hyperpolarization Activated Current via PKA and Calcineurin
title_full_unstemmed Tonic 5nM DA Stabilizes Neuronal Output by Enabling Bidirectional Activity-Dependent Regulation of the Hyperpolarization Activated Current via PKA and Calcineurin
title_short Tonic 5nM DA Stabilizes Neuronal Output by Enabling Bidirectional Activity-Dependent Regulation of the Hyperpolarization Activated Current via PKA and Calcineurin
title_sort tonic 5nm da stabilizes neuronal output by enabling bidirectional activity-dependent regulation of the hyperpolarization activated current via pka and calcineurin
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4333293/
https://www.ncbi.nlm.nih.gov/pubmed/25692473
http://dx.doi.org/10.1371/journal.pone.0117965
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