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High Frequency Oscillations in Rat Hippocampal Slices: Origin, Frequency Characteristics, and Spread

Field potential oscillations reflect repetitive firing and synaptic activity by ensembles of neurons in certain areas of the brain. They can be distinguished as slow (e.g., alpha, delta, and theta), fast (e.g., beta and gamma), and high frequency oscillations (HFOs). Neuronal oscillations are involv...

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Autores principales: Naggar, Isaac, Stewart, Mark, Orman, Rena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7188778/
https://www.ncbi.nlm.nih.gov/pubmed/32390935
http://dx.doi.org/10.3389/fneur.2020.00326
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author Naggar, Isaac
Stewart, Mark
Orman, Rena
author_facet Naggar, Isaac
Stewart, Mark
Orman, Rena
author_sort Naggar, Isaac
collection PubMed
description Field potential oscillations reflect repetitive firing and synaptic activity by ensembles of neurons in certain areas of the brain. They can be distinguished as slow (e.g., alpha, delta, and theta), fast (e.g., beta and gamma), and high frequency oscillations (HFOs). Neuronal oscillations are involved in a variety of physiological and pathophysiological states such as cognition, consciousness, and seizures. The laminar structure of rat hippocampus affords a way to study these oscillations in hippocampal slices. Rat ventral hippocampal brain slices were cut and maintained in a recording chamber that permitted 64 simultaneous extracellular recordings in the presence of artificial CSF. Brief single stimulus pulses were applied with bipolar electrodes to the CA3 or CA1 regions of hippocampus. Single pulses triggered epileptiform population events that included HFOs in the 150–250 Hz range in the presence of GABA(A) receptor blockade or kainic acid. HFOs also occurred spontaneously in the presence of kainic acid. The oscillations had the largest amplitude in the CA3c cell layer, regardless of the drug, and were synchronized throughout the cell layer. AMPA receptor blockade stopped these HFOs, whereas NMDA receptor blockade did not. Gap junction activation did not restore HFOs in the presence of AMPA receptor blockade. Our findings suggest that a population of excitatory neurons in CA3c may be a primary focus of seizure-like activity in Ammon's Horn. We suggest that the interconnection of CA3c is different from the rest of CA3.
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spelling pubmed-71887782020-05-08 High Frequency Oscillations in Rat Hippocampal Slices: Origin, Frequency Characteristics, and Spread Naggar, Isaac Stewart, Mark Orman, Rena Front Neurol Neurology Field potential oscillations reflect repetitive firing and synaptic activity by ensembles of neurons in certain areas of the brain. They can be distinguished as slow (e.g., alpha, delta, and theta), fast (e.g., beta and gamma), and high frequency oscillations (HFOs). Neuronal oscillations are involved in a variety of physiological and pathophysiological states such as cognition, consciousness, and seizures. The laminar structure of rat hippocampus affords a way to study these oscillations in hippocampal slices. Rat ventral hippocampal brain slices were cut and maintained in a recording chamber that permitted 64 simultaneous extracellular recordings in the presence of artificial CSF. Brief single stimulus pulses were applied with bipolar electrodes to the CA3 or CA1 regions of hippocampus. Single pulses triggered epileptiform population events that included HFOs in the 150–250 Hz range in the presence of GABA(A) receptor blockade or kainic acid. HFOs also occurred spontaneously in the presence of kainic acid. The oscillations had the largest amplitude in the CA3c cell layer, regardless of the drug, and were synchronized throughout the cell layer. AMPA receptor blockade stopped these HFOs, whereas NMDA receptor blockade did not. Gap junction activation did not restore HFOs in the presence of AMPA receptor blockade. Our findings suggest that a population of excitatory neurons in CA3c may be a primary focus of seizure-like activity in Ammon's Horn. We suggest that the interconnection of CA3c is different from the rest of CA3. Frontiers Media S.A. 2020-04-22 /pmc/articles/PMC7188778/ /pubmed/32390935 http://dx.doi.org/10.3389/fneur.2020.00326 Text en Copyright © 2020 Naggar, Stewart and Orman. 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 Neurology
Naggar, Isaac
Stewart, Mark
Orman, Rena
High Frequency Oscillations in Rat Hippocampal Slices: Origin, Frequency Characteristics, and Spread
title High Frequency Oscillations in Rat Hippocampal Slices: Origin, Frequency Characteristics, and Spread
title_full High Frequency Oscillations in Rat Hippocampal Slices: Origin, Frequency Characteristics, and Spread
title_fullStr High Frequency Oscillations in Rat Hippocampal Slices: Origin, Frequency Characteristics, and Spread
title_full_unstemmed High Frequency Oscillations in Rat Hippocampal Slices: Origin, Frequency Characteristics, and Spread
title_short High Frequency Oscillations in Rat Hippocampal Slices: Origin, Frequency Characteristics, and Spread
title_sort high frequency oscillations in rat hippocampal slices: origin, frequency characteristics, and spread
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7188778/
https://www.ncbi.nlm.nih.gov/pubmed/32390935
http://dx.doi.org/10.3389/fneur.2020.00326
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