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Seizure-Induced Arc mRNA Expression Thresholds in Rat Hippocampus and Perirhinal Cortex

Immediate-early genes (IEGs) are rapidly and transiently induced following excitatory neuronal activity including maximal electroconvulsive shock treatment (ECT). The rapid RNA response can be blocked by the sodium channel antagonist tetrodotoxin (TTX), without blocking seizures, indicating a role f...

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Autores principales: Chawla, Monica K., Gray, Daniel T., Nguyen, Christie, Dhaliwal, Harshaan, Zempare, Marc, Okuno, Hiroyuki, Huentelman, Matthew J., Barnes, Carol A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6221912/
https://www.ncbi.nlm.nih.gov/pubmed/30443206
http://dx.doi.org/10.3389/fnsys.2018.00053
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author Chawla, Monica K.
Gray, Daniel T.
Nguyen, Christie
Dhaliwal, Harshaan
Zempare, Marc
Okuno, Hiroyuki
Huentelman, Matthew J.
Barnes, Carol A.
author_facet Chawla, Monica K.
Gray, Daniel T.
Nguyen, Christie
Dhaliwal, Harshaan
Zempare, Marc
Okuno, Hiroyuki
Huentelman, Matthew J.
Barnes, Carol A.
author_sort Chawla, Monica K.
collection PubMed
description Immediate-early genes (IEGs) are rapidly and transiently induced following excitatory neuronal activity including maximal electroconvulsive shock treatment (ECT). The rapid RNA response can be blocked by the sodium channel antagonist tetrodotoxin (TTX), without blocking seizures, indicating a role for electrical stimulation in electroconvulsive shock-induced mRNA responses. In behaving animals, Arc mRNA is selectively transcribed following patterned neuronal activity and rapidly trafficked to dendrites where it preferentially accumulates at active synapses for local translation. Here we examined whether there is a relationship between the current intensities that elicit seizures and the threshold for Arc mRNA transcription in the rat hippocampus and perirhinal cortex (PRC). Animals received ECT of varying current intensities (0, 20, 40 65, 77 and 85 mA) and were sacrificed 5 min later. While significantly more CA1, CA3 and perirhinal pyramidal cells expressed Arc at the lowest stimulus intensity compared to granule cells, there was an abrupt threshold transition that occurred in all four regions at 77 mA. This precise threshold for Arc expression in all temporal lobe neurons examined may involve regulation of the calcium-dependent mechanisms that are upstream to activity-dependent IEG transcription.
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spelling pubmed-62219122018-11-15 Seizure-Induced Arc mRNA Expression Thresholds in Rat Hippocampus and Perirhinal Cortex Chawla, Monica K. Gray, Daniel T. Nguyen, Christie Dhaliwal, Harshaan Zempare, Marc Okuno, Hiroyuki Huentelman, Matthew J. Barnes, Carol A. Front Syst Neurosci Neuroscience Immediate-early genes (IEGs) are rapidly and transiently induced following excitatory neuronal activity including maximal electroconvulsive shock treatment (ECT). The rapid RNA response can be blocked by the sodium channel antagonist tetrodotoxin (TTX), without blocking seizures, indicating a role for electrical stimulation in electroconvulsive shock-induced mRNA responses. In behaving animals, Arc mRNA is selectively transcribed following patterned neuronal activity and rapidly trafficked to dendrites where it preferentially accumulates at active synapses for local translation. Here we examined whether there is a relationship between the current intensities that elicit seizures and the threshold for Arc mRNA transcription in the rat hippocampus and perirhinal cortex (PRC). Animals received ECT of varying current intensities (0, 20, 40 65, 77 and 85 mA) and were sacrificed 5 min later. While significantly more CA1, CA3 and perirhinal pyramidal cells expressed Arc at the lowest stimulus intensity compared to granule cells, there was an abrupt threshold transition that occurred in all four regions at 77 mA. This precise threshold for Arc expression in all temporal lobe neurons examined may involve regulation of the calcium-dependent mechanisms that are upstream to activity-dependent IEG transcription. Frontiers Media S.A. 2018-11-01 /pmc/articles/PMC6221912/ /pubmed/30443206 http://dx.doi.org/10.3389/fnsys.2018.00053 Text en Copyright © 2018 Chawla, Gray, Nguyen, Dhaliwal, Zempare, Okuno, Huentelman and Barnes. http://creativecommons.org/licenses/by/4.0/ 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) and the copyright owner(s) 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
Chawla, Monica K.
Gray, Daniel T.
Nguyen, Christie
Dhaliwal, Harshaan
Zempare, Marc
Okuno, Hiroyuki
Huentelman, Matthew J.
Barnes, Carol A.
Seizure-Induced Arc mRNA Expression Thresholds in Rat Hippocampus and Perirhinal Cortex
title Seizure-Induced Arc mRNA Expression Thresholds in Rat Hippocampus and Perirhinal Cortex
title_full Seizure-Induced Arc mRNA Expression Thresholds in Rat Hippocampus and Perirhinal Cortex
title_fullStr Seizure-Induced Arc mRNA Expression Thresholds in Rat Hippocampus and Perirhinal Cortex
title_full_unstemmed Seizure-Induced Arc mRNA Expression Thresholds in Rat Hippocampus and Perirhinal Cortex
title_short Seizure-Induced Arc mRNA Expression Thresholds in Rat Hippocampus and Perirhinal Cortex
title_sort seizure-induced arc mrna expression thresholds in rat hippocampus and perirhinal cortex
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6221912/
https://www.ncbi.nlm.nih.gov/pubmed/30443206
http://dx.doi.org/10.3389/fnsys.2018.00053
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