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mGluR1 Regulates the Interspike Interval Threshold for Dendritic Ca(2+) Transients in the Cerebellar Purkinje Cells
Ca(2+) transients can be observed in the distal dendrites of Purkinje cells (PCs) despite their lack of action potential backpropagation. These Ca(2+) events in distal dendrites require specific patterns of PC firing, such as complex spikes (CS) or simple spikes (SS) of burst mode. Unlike CS, which...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Korean Society for Brain and Neural Sciences
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10175955/ https://www.ncbi.nlm.nih.gov/pubmed/37164648 http://dx.doi.org/10.5607/en22040 |
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author | Jang, Dong Cheol Ryu, Changhyeon Chung, Geehoon Kim, Sun Kwang Kim, Sang Jeong |
author_facet | Jang, Dong Cheol Ryu, Changhyeon Chung, Geehoon Kim, Sun Kwang Kim, Sang Jeong |
author_sort | Jang, Dong Cheol |
collection | PubMed |
description | Ca(2+) transients can be observed in the distal dendrites of Purkinje cells (PCs) despite their lack of action potential backpropagation. These Ca(2+) events in distal dendrites require specific patterns of PC firing, such as complex spikes (CS) or simple spikes (SS) of burst mode. Unlike CS, which can act directly on voltage-gated calcium channels in the dendrites through climbing fiber inputs, the condition that can produce the Ca(2+) events in distal dendrites with burst mode SS is poorly understood. Here, we propose the interspike interval threshold (ISIT) for Ca(2+) transients in the distal dendrites of PC. We found that to induce the Ca(2+) transients in distal dendrites the frequency of spike firing of PC should reach 250 Hz (3 ms ISI). Metabotropic glutamate receptor 1 (mGluR1) activation significantly relieved the ISIT and established cellular conditions in which spike firing with 50 Hz (19 ms ISI) could induce Ca(2+) transients in the distal dendrites. In contrast, blocking T-type Ca(2+) channels or depleting the endoplasmic reticulum Ca(2+) store resulted in a stricter condition in which spike firing with 333 Hz (2 ms ISI) was required. Our findings demonstrate that the PC has strict ISIT for dendritic Ca(2+) transients, and this ISIT can be relieved by mGluR1 activation. This strict restriction of ISIT could contribute to the reduction of the signal-to-noise ratio in terms of collecting information by preventing excessive dendritic Ca(2+) transients through the spontaneous activity of PC. |
format | Online Article Text |
id | pubmed-10175955 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Korean Society for Brain and Neural Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-101759552023-05-13 mGluR1 Regulates the Interspike Interval Threshold for Dendritic Ca(2+) Transients in the Cerebellar Purkinje Cells Jang, Dong Cheol Ryu, Changhyeon Chung, Geehoon Kim, Sun Kwang Kim, Sang Jeong Exp Neurobiol Short Communication Ca(2+) transients can be observed in the distal dendrites of Purkinje cells (PCs) despite their lack of action potential backpropagation. These Ca(2+) events in distal dendrites require specific patterns of PC firing, such as complex spikes (CS) or simple spikes (SS) of burst mode. Unlike CS, which can act directly on voltage-gated calcium channels in the dendrites through climbing fiber inputs, the condition that can produce the Ca(2+) events in distal dendrites with burst mode SS is poorly understood. Here, we propose the interspike interval threshold (ISIT) for Ca(2+) transients in the distal dendrites of PC. We found that to induce the Ca(2+) transients in distal dendrites the frequency of spike firing of PC should reach 250 Hz (3 ms ISI). Metabotropic glutamate receptor 1 (mGluR1) activation significantly relieved the ISIT and established cellular conditions in which spike firing with 50 Hz (19 ms ISI) could induce Ca(2+) transients in the distal dendrites. In contrast, blocking T-type Ca(2+) channels or depleting the endoplasmic reticulum Ca(2+) store resulted in a stricter condition in which spike firing with 333 Hz (2 ms ISI) was required. Our findings demonstrate that the PC has strict ISIT for dendritic Ca(2+) transients, and this ISIT can be relieved by mGluR1 activation. This strict restriction of ISIT could contribute to the reduction of the signal-to-noise ratio in terms of collecting information by preventing excessive dendritic Ca(2+) transients through the spontaneous activity of PC. The Korean Society for Brain and Neural Sciences 2023-04-30 2023-04-30 /pmc/articles/PMC10175955/ /pubmed/37164648 http://dx.doi.org/10.5607/en22040 Text en Copyright © Experimental Neurobiology 2023 https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Short Communication Jang, Dong Cheol Ryu, Changhyeon Chung, Geehoon Kim, Sun Kwang Kim, Sang Jeong mGluR1 Regulates the Interspike Interval Threshold for Dendritic Ca(2+) Transients in the Cerebellar Purkinje Cells |
title | mGluR1 Regulates the Interspike Interval Threshold for Dendritic Ca(2+) Transients in the Cerebellar Purkinje Cells |
title_full | mGluR1 Regulates the Interspike Interval Threshold for Dendritic Ca(2+) Transients in the Cerebellar Purkinje Cells |
title_fullStr | mGluR1 Regulates the Interspike Interval Threshold for Dendritic Ca(2+) Transients in the Cerebellar Purkinje Cells |
title_full_unstemmed | mGluR1 Regulates the Interspike Interval Threshold for Dendritic Ca(2+) Transients in the Cerebellar Purkinje Cells |
title_short | mGluR1 Regulates the Interspike Interval Threshold for Dendritic Ca(2+) Transients in the Cerebellar Purkinje Cells |
title_sort | mglur1 regulates the interspike interval threshold for dendritic ca(2+) transients in the cerebellar purkinje cells |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10175955/ https://www.ncbi.nlm.nih.gov/pubmed/37164648 http://dx.doi.org/10.5607/en22040 |
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