KV7 Channels Regulate Firing during Synaptic Integration in GABAergic Striatal Neurons

Striatal projection neurons (SPNs) process motor and cognitive information. Their activity is affected by Parkinson’s disease, in which dopamine concentration is decreased and acetylcholine concentration is increased. Acetylcholine activates muscarinic receptors in SPNs. Its main source is the choli...

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Main Authors: M. Belén Pérez-Ramírez, Antonio Laville, Dagoberto Tapia, Mariana Duhne, Esther Lara-González, José Bargas, Elvira Galarraga
Format: Article
Language:English
Published: Wiley 2015-01-01
Series:Neural Plasticity
Online Access:http://dx.doi.org/10.1155/2015/472676
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author M. Belén Pérez-Ramírez
Antonio Laville
Dagoberto Tapia
Mariana Duhne
Esther Lara-González
José Bargas
Elvira Galarraga
author_facet M. Belén Pérez-Ramírez
Antonio Laville
Dagoberto Tapia
Mariana Duhne
Esther Lara-González
José Bargas
Elvira Galarraga
author_sort M. Belén Pérez-Ramírez
collection DOAJ
description Striatal projection neurons (SPNs) process motor and cognitive information. Their activity is affected by Parkinson’s disease, in which dopamine concentration is decreased and acetylcholine concentration is increased. Acetylcholine activates muscarinic receptors in SPNs. Its main source is the cholinergic interneuron that responds with a briefer latency than SPNs during a cortical command. Therefore, an important question is whether muscarinic G-protein coupled receptors and their signaling cascades are fast enough to intervene during synaptic responses to regulate synaptic integration and firing. One of the most known voltage dependent channels regulated by muscarinic receptors is the KV7/KCNQ channel. It is not known whether these channels regulate the integration of suprathreshold corticostriatal responses. Here, we study the impact of cholinergic muscarinic modulation on the synaptic response of SPNs by regulating KV7 channels. We found that KV7 channels regulate corticostriatal synaptic integration and that this modulation occurs in the dendritic/spines compartment. In contrast, it is negligible in the somatic compartment. This modulation occurs on sub- and suprathreshold responses and lasts during the whole duration of the responses, hundreds of milliseconds, greatly altering SPNs firing properties. This modulation affected the behavior of the striatal microcircuit.
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institution Kabale University
issn 2090-5904
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spelling doaj-art-095205aa76444ccc9f21a43d9a6654fa2025-02-03T01:22:55ZengWileyNeural Plasticity2090-59041687-54432015-01-01201510.1155/2015/472676472676KV7 Channels Regulate Firing during Synaptic Integration in GABAergic Striatal NeuronsM. Belén Pérez-Ramírez0Antonio Laville1Dagoberto Tapia2Mariana Duhne3Esther Lara-González4José Bargas5Elvira Galarraga6División de Neurociencias, Instituto de Fisiología Celular, Universidad Nacional Autónoma de México, 04510 México City, DF, MexicoDivisión de Neurociencias, Instituto de Fisiología Celular, Universidad Nacional Autónoma de México, 04510 México City, DF, MexicoDivisión de Neurociencias, Instituto de Fisiología Celular, Universidad Nacional Autónoma de México, 04510 México City, DF, MexicoDivisión de Neurociencias, Instituto de Fisiología Celular, Universidad Nacional Autónoma de México, 04510 México City, DF, MexicoDivisión de Neurociencias, Instituto de Fisiología Celular, Universidad Nacional Autónoma de México, 04510 México City, DF, MexicoDivisión de Neurociencias, Instituto de Fisiología Celular, Universidad Nacional Autónoma de México, 04510 México City, DF, MexicoDivisión de Neurociencias, Instituto de Fisiología Celular, Universidad Nacional Autónoma de México, 04510 México City, DF, MexicoStriatal projection neurons (SPNs) process motor and cognitive information. Their activity is affected by Parkinson’s disease, in which dopamine concentration is decreased and acetylcholine concentration is increased. Acetylcholine activates muscarinic receptors in SPNs. Its main source is the cholinergic interneuron that responds with a briefer latency than SPNs during a cortical command. Therefore, an important question is whether muscarinic G-protein coupled receptors and their signaling cascades are fast enough to intervene during synaptic responses to regulate synaptic integration and firing. One of the most known voltage dependent channels regulated by muscarinic receptors is the KV7/KCNQ channel. It is not known whether these channels regulate the integration of suprathreshold corticostriatal responses. Here, we study the impact of cholinergic muscarinic modulation on the synaptic response of SPNs by regulating KV7 channels. We found that KV7 channels regulate corticostriatal synaptic integration and that this modulation occurs in the dendritic/spines compartment. In contrast, it is negligible in the somatic compartment. This modulation occurs on sub- and suprathreshold responses and lasts during the whole duration of the responses, hundreds of milliseconds, greatly altering SPNs firing properties. This modulation affected the behavior of the striatal microcircuit.http://dx.doi.org/10.1155/2015/472676
spellingShingle M. Belén Pérez-Ramírez
Antonio Laville
Dagoberto Tapia
Mariana Duhne
Esther Lara-González
José Bargas
Elvira Galarraga
KV7 Channels Regulate Firing during Synaptic Integration in GABAergic Striatal Neurons
Neural Plasticity
title KV7 Channels Regulate Firing during Synaptic Integration in GABAergic Striatal Neurons
title_full KV7 Channels Regulate Firing during Synaptic Integration in GABAergic Striatal Neurons
title_fullStr KV7 Channels Regulate Firing during Synaptic Integration in GABAergic Striatal Neurons
title_full_unstemmed KV7 Channels Regulate Firing during Synaptic Integration in GABAergic Striatal Neurons
title_short KV7 Channels Regulate Firing during Synaptic Integration in GABAergic Striatal Neurons
title_sort kv7 channels regulate firing during synaptic integration in gabaergic striatal neurons
url http://dx.doi.org/10.1155/2015/472676
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