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Muscarinic Modulation of High Frequency Oscillations in Pedunculopontine Neurons
We previously reported that persistent application of the non-specific cholinergic agonist carbachol (CAR) increased the frequency of calcium channel-mediated oscillatory activity in pedunculopontine nucleus (PPN) neurons, which we identified as dependent on voltage-gated, high-threshold P/Q-type ch...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3818577/ https://www.ncbi.nlm.nih.gov/pubmed/24223570 http://dx.doi.org/10.3389/fneur.2013.00176 |
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author | Kezunovic, Nebojsa Hyde, James Goitia, Belen Bisagno, Veronica Urbano, Francisco J. Garcia-Rill, Edgar |
author_facet | Kezunovic, Nebojsa Hyde, James Goitia, Belen Bisagno, Veronica Urbano, Francisco J. Garcia-Rill, Edgar |
author_sort | Kezunovic, Nebojsa |
collection | PubMed |
description | We previously reported that persistent application of the non-specific cholinergic agonist carbachol (CAR) increased the frequency of calcium channel-mediated oscillatory activity in pedunculopontine nucleus (PPN) neurons, which we identified as dependent on voltage-gated, high-threshold P/Q-type channels. Here, we tested the hypothesis that M2 muscarinic receptors and G-proteins associated with M2 receptors mediate the increase in oscillatory frequency in PPN neurons. We found, using depolarizing ramps, that patch clamped 9–12 day old rat PPN neurons (n = 189) reached their peak oscillatory activity around −20 mV membrane potential. Acute (short duration) application of CAR blocked the oscillatory activity through M2 muscarinic receptors, an effect blocked by atropine. However, persistent (long duration) application of CAR significantly increased the frequency of oscillatory activity in PPN neurons through M2 receptors [40 ± 1 Hz (with CAR) vs. 23 ± 1 Hz (without CAR); p < 0.001]. We then tested the effects of the G-protein antagonist guanosine 5′-[β-thio] diphosphate trilithium salt (GDP-β-S), and the G-protein agonist 5′-[γ-thio] triphosphate trilithium salt (GTP-γ-S). We found, using a three-step protocol in voltage-clamp mode, that the increase in the frequency of oscillations induced by M2 cholinergic receptors was linked to a voltage-dependent G-protein mechanism. In summary, these results suggest that persistent cholinergic input creates a permissive activation state in the PPN that allows high frequency P/Q-type calcium channel-mediated gamma oscillations to occur. |
format | Online Article Text |
id | pubmed-3818577 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-38185772013-11-09 Muscarinic Modulation of High Frequency Oscillations in Pedunculopontine Neurons Kezunovic, Nebojsa Hyde, James Goitia, Belen Bisagno, Veronica Urbano, Francisco J. Garcia-Rill, Edgar Front Neurol Neuroscience We previously reported that persistent application of the non-specific cholinergic agonist carbachol (CAR) increased the frequency of calcium channel-mediated oscillatory activity in pedunculopontine nucleus (PPN) neurons, which we identified as dependent on voltage-gated, high-threshold P/Q-type channels. Here, we tested the hypothesis that M2 muscarinic receptors and G-proteins associated with M2 receptors mediate the increase in oscillatory frequency in PPN neurons. We found, using depolarizing ramps, that patch clamped 9–12 day old rat PPN neurons (n = 189) reached their peak oscillatory activity around −20 mV membrane potential. Acute (short duration) application of CAR blocked the oscillatory activity through M2 muscarinic receptors, an effect blocked by atropine. However, persistent (long duration) application of CAR significantly increased the frequency of oscillatory activity in PPN neurons through M2 receptors [40 ± 1 Hz (with CAR) vs. 23 ± 1 Hz (without CAR); p < 0.001]. We then tested the effects of the G-protein antagonist guanosine 5′-[β-thio] diphosphate trilithium salt (GDP-β-S), and the G-protein agonist 5′-[γ-thio] triphosphate trilithium salt (GTP-γ-S). We found, using a three-step protocol in voltage-clamp mode, that the increase in the frequency of oscillations induced by M2 cholinergic receptors was linked to a voltage-dependent G-protein mechanism. In summary, these results suggest that persistent cholinergic input creates a permissive activation state in the PPN that allows high frequency P/Q-type calcium channel-mediated gamma oscillations to occur. Frontiers Media S.A. 2013-11-06 /pmc/articles/PMC3818577/ /pubmed/24223570 http://dx.doi.org/10.3389/fneur.2013.00176 Text en Copyright © 2013 Kezunovic, Hyde, Goitia, Bisagno, Urbano and Garcia-Rill. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Kezunovic, Nebojsa Hyde, James Goitia, Belen Bisagno, Veronica Urbano, Francisco J. Garcia-Rill, Edgar Muscarinic Modulation of High Frequency Oscillations in Pedunculopontine Neurons |
title | Muscarinic Modulation of High Frequency Oscillations in Pedunculopontine Neurons |
title_full | Muscarinic Modulation of High Frequency Oscillations in Pedunculopontine Neurons |
title_fullStr | Muscarinic Modulation of High Frequency Oscillations in Pedunculopontine Neurons |
title_full_unstemmed | Muscarinic Modulation of High Frequency Oscillations in Pedunculopontine Neurons |
title_short | Muscarinic Modulation of High Frequency Oscillations in Pedunculopontine Neurons |
title_sort | muscarinic modulation of high frequency oscillations in pedunculopontine neurons |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3818577/ https://www.ncbi.nlm.nih.gov/pubmed/24223570 http://dx.doi.org/10.3389/fneur.2013.00176 |
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