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Altered glutamatergic tone reveals two distinct resting state networks at the cellular level in hippocampal sclerosis
Hippocampal sclerosis (HS), the most common subset of drug-resistant epilepsy (DRE), is associated with large-scale network abnormalities, even under resting state. We studied the excitatory postsynaptic currents (EPSCs) recorded from pyramidal neurons in resected samples under resting conditions fr...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5428248/ https://www.ncbi.nlm.nih.gov/pubmed/28336943 http://dx.doi.org/10.1038/s41598-017-00358-7 |
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author | Banerjee, Jyotirmoy BanerjeeDixit, Aparna Srivastava, Arpna Ramanujam, Bhargavi Kakkar, Aanchal Sarkar, Chitra Tripathi, Manjari Chandra, P. Sarat |
author_facet | Banerjee, Jyotirmoy BanerjeeDixit, Aparna Srivastava, Arpna Ramanujam, Bhargavi Kakkar, Aanchal Sarkar, Chitra Tripathi, Manjari Chandra, P. Sarat |
author_sort | Banerjee, Jyotirmoy |
collection | PubMed |
description | Hippocampal sclerosis (HS), the most common subset of drug-resistant epilepsy (DRE), is associated with large-scale network abnormalities, even under resting state. We studied the excitatory postsynaptic currents (EPSCs) recorded from pyramidal neurons in resected samples under resting conditions from the hippocampal and anterior temporal lobe (ATL) obtained from patients with HS (n = 14) undergoing resective surgery. We observed higher frequency and amplitude of spontaneous EPSCs in both the samples compared to non-seizure control samples. Application of tetrodotoxin (TTX) reduced the frequency of spontaneous EPSCs by 49.6 ± 4.3% and 61.8 ± 6.2% in the hippocampal and ATL samples, respectively. The magnitude of reduction caused by TTX with respect to non-seizure controls was significantly higher in the ATL samples than in the hippocampal samples. The magnitude of the change in the expression of the NR2A subunit of the NMDA receptors also varied in these two regions. Thus, the mechanism of hyperexcitabilty mediated by glutamatergic network reorganization in the hippocampal region is different from that in the ATL region of patients with HS, suggesting two independent resting-state networks at the cellular level. Taken together, these findings will improve the understanding of the broadly distributed resting-state networks in HS. |
format | Online Article Text |
id | pubmed-5428248 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-54282482017-05-15 Altered glutamatergic tone reveals two distinct resting state networks at the cellular level in hippocampal sclerosis Banerjee, Jyotirmoy BanerjeeDixit, Aparna Srivastava, Arpna Ramanujam, Bhargavi Kakkar, Aanchal Sarkar, Chitra Tripathi, Manjari Chandra, P. Sarat Sci Rep Article Hippocampal sclerosis (HS), the most common subset of drug-resistant epilepsy (DRE), is associated with large-scale network abnormalities, even under resting state. We studied the excitatory postsynaptic currents (EPSCs) recorded from pyramidal neurons in resected samples under resting conditions from the hippocampal and anterior temporal lobe (ATL) obtained from patients with HS (n = 14) undergoing resective surgery. We observed higher frequency and amplitude of spontaneous EPSCs in both the samples compared to non-seizure control samples. Application of tetrodotoxin (TTX) reduced the frequency of spontaneous EPSCs by 49.6 ± 4.3% and 61.8 ± 6.2% in the hippocampal and ATL samples, respectively. The magnitude of reduction caused by TTX with respect to non-seizure controls was significantly higher in the ATL samples than in the hippocampal samples. The magnitude of the change in the expression of the NR2A subunit of the NMDA receptors also varied in these two regions. Thus, the mechanism of hyperexcitabilty mediated by glutamatergic network reorganization in the hippocampal region is different from that in the ATL region of patients with HS, suggesting two independent resting-state networks at the cellular level. Taken together, these findings will improve the understanding of the broadly distributed resting-state networks in HS. Nature Publishing Group UK 2017-03-23 /pmc/articles/PMC5428248/ /pubmed/28336943 http://dx.doi.org/10.1038/s41598-017-00358-7 Text en © The Author(s) 2017 This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Banerjee, Jyotirmoy BanerjeeDixit, Aparna Srivastava, Arpna Ramanujam, Bhargavi Kakkar, Aanchal Sarkar, Chitra Tripathi, Manjari Chandra, P. Sarat Altered glutamatergic tone reveals two distinct resting state networks at the cellular level in hippocampal sclerosis |
title | Altered glutamatergic tone reveals two distinct resting state networks at the cellular level in hippocampal sclerosis |
title_full | Altered glutamatergic tone reveals two distinct resting state networks at the cellular level in hippocampal sclerosis |
title_fullStr | Altered glutamatergic tone reveals two distinct resting state networks at the cellular level in hippocampal sclerosis |
title_full_unstemmed | Altered glutamatergic tone reveals two distinct resting state networks at the cellular level in hippocampal sclerosis |
title_short | Altered glutamatergic tone reveals two distinct resting state networks at the cellular level in hippocampal sclerosis |
title_sort | altered glutamatergic tone reveals two distinct resting state networks at the cellular level in hippocampal sclerosis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5428248/ https://www.ncbi.nlm.nih.gov/pubmed/28336943 http://dx.doi.org/10.1038/s41598-017-00358-7 |
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