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Firing Behavior and Network Activity of Single Neurons in Human Epileptic Hypothalamic Hamartoma
Objective: Human hypothalamic hamartomas (HH) are intrinsically epileptogenic and are associated with treatment-resistant gelastic seizures. The basic cellular mechanisms responsible for seizure onset within HH are unknown. We used intra-operative microwire recordings of single neuron activity to me...
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/PMC3873534/ https://www.ncbi.nlm.nih.gov/pubmed/24409165 http://dx.doi.org/10.3389/fneur.2013.00210 |
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author | Steinmetz, Peter N. Wait, Scott D. Lekovic, Gregory P. Rekate, Harold L. Kerrigan, John F. |
author_facet | Steinmetz, Peter N. Wait, Scott D. Lekovic, Gregory P. Rekate, Harold L. Kerrigan, John F. |
author_sort | Steinmetz, Peter N. |
collection | PubMed |
description | Objective: Human hypothalamic hamartomas (HH) are intrinsically epileptogenic and are associated with treatment-resistant gelastic seizures. The basic cellular mechanisms responsible for seizure onset within HH are unknown. We used intra-operative microwire recordings of single neuron activity to measure the spontaneous firing rate of neurons and the degree of functional connection between neurons within the tumor. Technique: Fourteen patients underwent transventricular endoscopic resection of HH for treatment-resistant epilepsy. Prior to surgical resection, single neuron recordings from bundled microwires (total of nine contacts) were obtained from HH tissue. Spontaneous activity was recorded for two or three 5-min epochs under steady-state general anesthesia. Off-line analysis included cluster analysis of single unit activity and probability analysis of firing relationships between pairs of neurons. Results: Altogether, 222 neurons were identified (mean 6 neurons per recording epoch). Cluster analysis of single neuron firing utilizing a mixture of Gaussians model identified two distinct populations on the basis of firing rate (median firing frequency 0.6 versus 15.0 spikes per second; p < 10(−5)). Cluster analysis identified three populations determined by levels of burst firing (median burst indices of 0.015, 0.18, and 0.39; p < 10(−15)). Unbiased analysis of spontaneous single unit behavior showed that 51% of all possible neuron pairs within each recording epoch had a significant level of firing synchrony (p < 10(−15)). The subgroup of neurons with higher median firing frequencies was more likely to demonstrate synchronous firing (p < 10(−7)). Conclusion: Hypothalamic hamartoma tissue in vivo contains neurons which fire spontaneously. The activity of single neurons is diverse but distributes into at least two electrophysiological phenoytpes. Functional linkage between single neurons suggests that HH neurons exist within local networks that may contribute to ictogenesis. |
format | Online Article Text |
id | pubmed-3873534 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-38735342014-01-09 Firing Behavior and Network Activity of Single Neurons in Human Epileptic Hypothalamic Hamartoma Steinmetz, Peter N. Wait, Scott D. Lekovic, Gregory P. Rekate, Harold L. Kerrigan, John F. Front Neurol Neuroscience Objective: Human hypothalamic hamartomas (HH) are intrinsically epileptogenic and are associated with treatment-resistant gelastic seizures. The basic cellular mechanisms responsible for seizure onset within HH are unknown. We used intra-operative microwire recordings of single neuron activity to measure the spontaneous firing rate of neurons and the degree of functional connection between neurons within the tumor. Technique: Fourteen patients underwent transventricular endoscopic resection of HH for treatment-resistant epilepsy. Prior to surgical resection, single neuron recordings from bundled microwires (total of nine contacts) were obtained from HH tissue. Spontaneous activity was recorded for two or three 5-min epochs under steady-state general anesthesia. Off-line analysis included cluster analysis of single unit activity and probability analysis of firing relationships between pairs of neurons. Results: Altogether, 222 neurons were identified (mean 6 neurons per recording epoch). Cluster analysis of single neuron firing utilizing a mixture of Gaussians model identified two distinct populations on the basis of firing rate (median firing frequency 0.6 versus 15.0 spikes per second; p < 10(−5)). Cluster analysis identified three populations determined by levels of burst firing (median burst indices of 0.015, 0.18, and 0.39; p < 10(−15)). Unbiased analysis of spontaneous single unit behavior showed that 51% of all possible neuron pairs within each recording epoch had a significant level of firing synchrony (p < 10(−15)). The subgroup of neurons with higher median firing frequencies was more likely to demonstrate synchronous firing (p < 10(−7)). Conclusion: Hypothalamic hamartoma tissue in vivo contains neurons which fire spontaneously. The activity of single neurons is diverse but distributes into at least two electrophysiological phenoytpes. Functional linkage between single neurons suggests that HH neurons exist within local networks that may contribute to ictogenesis. Frontiers Media S.A. 2013-12-27 /pmc/articles/PMC3873534/ /pubmed/24409165 http://dx.doi.org/10.3389/fneur.2013.00210 Text en Copyright © 2013 Steinmetz, Wait, Lekovic, Rekate and Kerrigan. 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 Steinmetz, Peter N. Wait, Scott D. Lekovic, Gregory P. Rekate, Harold L. Kerrigan, John F. Firing Behavior and Network Activity of Single Neurons in Human Epileptic Hypothalamic Hamartoma |
title | Firing Behavior and Network Activity of Single Neurons in Human Epileptic Hypothalamic Hamartoma |
title_full | Firing Behavior and Network Activity of Single Neurons in Human Epileptic Hypothalamic Hamartoma |
title_fullStr | Firing Behavior and Network Activity of Single Neurons in Human Epileptic Hypothalamic Hamartoma |
title_full_unstemmed | Firing Behavior and Network Activity of Single Neurons in Human Epileptic Hypothalamic Hamartoma |
title_short | Firing Behavior and Network Activity of Single Neurons in Human Epileptic Hypothalamic Hamartoma |
title_sort | firing behavior and network activity of single neurons in human epileptic hypothalamic hamartoma |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3873534/ https://www.ncbi.nlm.nih.gov/pubmed/24409165 http://dx.doi.org/10.3389/fneur.2013.00210 |
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