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Duration differences of corticostriatal responses in striatal projection neurons depend on calcium activated potassium currents
The firing of striatal projection neurons (SPNs) exhibits afterhyperpolarizing potentials (AHPs) that determine discharge frequency. They are in part generated by Ca(2+)-activated K(+)-currents involving BK and SK components. It has previously been shown that suprathreshold corticostriatal responses...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3790310/ https://www.ncbi.nlm.nih.gov/pubmed/24109439 http://dx.doi.org/10.3389/fnsys.2013.00063 |
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author | Arias-García, Mario A. Tapia, Dagoberto Flores-Barrera, Edén Pérez-Ortega, Jesús E. Bargas, José Galarraga, Elvira |
author_facet | Arias-García, Mario A. Tapia, Dagoberto Flores-Barrera, Edén Pérez-Ortega, Jesús E. Bargas, José Galarraga, Elvira |
author_sort | Arias-García, Mario A. |
collection | PubMed |
description | The firing of striatal projection neurons (SPNs) exhibits afterhyperpolarizing potentials (AHPs) that determine discharge frequency. They are in part generated by Ca(2+)-activated K(+)-currents involving BK and SK components. It has previously been shown that suprathreshold corticostriatal responses are more prolonged and evoke more action potentials in direct pathway SPNs (dSPNs) than in indirect pathway SPNs (iSPNs). In contrast, iSPNs generate dendritic autoregenerative responses. Using whole cell recordings in brain slices, we asked whether the participation of Ca(2+)-activated K(+)-currents plays a role in these responses. Secondly, we asked if these currents may explain some differences in synaptic integration between dSPNs and iSPNs. Neurons obtained from BAC D(1) and D(2) GFP mice were recorded. We used charybdotoxin and apamin to block BK and SK channels, respectively. Both antagonists increased the depolarization and delayed the repolarization of suprathreshold corticostriatal responses in both neuron classes. We also used NS 1619 and NS 309 (CyPPA), to enhance BK and SK channels, respectively. Current enhancers hyperpolarized and accelerated the repolarization of corticostriatal responses in both neuron classes. Nevertheless, these drugs made evident that the contribution of Ca(2+)-activated K(+)-currents was different in dSPNs as compared to iSPNs: in dSPNs their activation was slower as though calcium took a diffusion delay to activate them. In contrast, their activation was fast and then sustained in iSPNs as though calcium flux activates them at the moment of entry. The blockade of Ca(2+)-activated K(+)-currents made iSPNs to look as dSPNs. Conversely, their enhancement made dSPNs to look as iSPNs. It is concluded that Ca(2+)-activated K(+)-currents are a main intrinsic determinant causing the differences in synaptic integration between corticostriatal polysynaptic responses between dSPNs and iSPNs. |
format | Online Article Text |
id | pubmed-3790310 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-37903102013-10-09 Duration differences of corticostriatal responses in striatal projection neurons depend on calcium activated potassium currents Arias-García, Mario A. Tapia, Dagoberto Flores-Barrera, Edén Pérez-Ortega, Jesús E. Bargas, José Galarraga, Elvira Front Syst Neurosci Neuroscience The firing of striatal projection neurons (SPNs) exhibits afterhyperpolarizing potentials (AHPs) that determine discharge frequency. They are in part generated by Ca(2+)-activated K(+)-currents involving BK and SK components. It has previously been shown that suprathreshold corticostriatal responses are more prolonged and evoke more action potentials in direct pathway SPNs (dSPNs) than in indirect pathway SPNs (iSPNs). In contrast, iSPNs generate dendritic autoregenerative responses. Using whole cell recordings in brain slices, we asked whether the participation of Ca(2+)-activated K(+)-currents plays a role in these responses. Secondly, we asked if these currents may explain some differences in synaptic integration between dSPNs and iSPNs. Neurons obtained from BAC D(1) and D(2) GFP mice were recorded. We used charybdotoxin and apamin to block BK and SK channels, respectively. Both antagonists increased the depolarization and delayed the repolarization of suprathreshold corticostriatal responses in both neuron classes. We also used NS 1619 and NS 309 (CyPPA), to enhance BK and SK channels, respectively. Current enhancers hyperpolarized and accelerated the repolarization of corticostriatal responses in both neuron classes. Nevertheless, these drugs made evident that the contribution of Ca(2+)-activated K(+)-currents was different in dSPNs as compared to iSPNs: in dSPNs their activation was slower as though calcium took a diffusion delay to activate them. In contrast, their activation was fast and then sustained in iSPNs as though calcium flux activates them at the moment of entry. The blockade of Ca(2+)-activated K(+)-currents made iSPNs to look as dSPNs. Conversely, their enhancement made dSPNs to look as iSPNs. It is concluded that Ca(2+)-activated K(+)-currents are a main intrinsic determinant causing the differences in synaptic integration between corticostriatal polysynaptic responses between dSPNs and iSPNs. Frontiers Media S.A. 2013-10-04 /pmc/articles/PMC3790310/ /pubmed/24109439 http://dx.doi.org/10.3389/fnsys.2013.00063 Text en Copyright © 2013 Arias-García, Tapia, Flores-Barrera, Pérez-Ortega, Bargas and Galarraga. 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 Arias-García, Mario A. Tapia, Dagoberto Flores-Barrera, Edén Pérez-Ortega, Jesús E. Bargas, José Galarraga, Elvira Duration differences of corticostriatal responses in striatal projection neurons depend on calcium activated potassium currents |
title | Duration differences of corticostriatal responses in striatal projection neurons depend on calcium activated potassium currents |
title_full | Duration differences of corticostriatal responses in striatal projection neurons depend on calcium activated potassium currents |
title_fullStr | Duration differences of corticostriatal responses in striatal projection neurons depend on calcium activated potassium currents |
title_full_unstemmed | Duration differences of corticostriatal responses in striatal projection neurons depend on calcium activated potassium currents |
title_short | Duration differences of corticostriatal responses in striatal projection neurons depend on calcium activated potassium currents |
title_sort | duration differences of corticostriatal responses in striatal projection neurons depend on calcium activated potassium currents |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3790310/ https://www.ncbi.nlm.nih.gov/pubmed/24109439 http://dx.doi.org/10.3389/fnsys.2013.00063 |
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