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Frequency-Domain Analysis of Intrinsic Neuronal Properties using High-Resistant Electrodes

Intrinsic cellular properties of neurons in culture or slices are usually studied by the whole cell clamp method using low-resistant patch pipettes. These electrodes allow detailed analyses with standard electrophysiological methods such as current- or voltage-clamp. However, in these preparations l...

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Autores principales: Rössert, Christian, Straka, Hans, Glasauer, Stefan, Moore, Lee E.
Formato: Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2858610/
https://www.ncbi.nlm.nih.gov/pubmed/20582288
http://dx.doi.org/10.3389/neuro.17.002.2009
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author Rössert, Christian
Straka, Hans
Glasauer, Stefan
Moore, Lee E.
author_facet Rössert, Christian
Straka, Hans
Glasauer, Stefan
Moore, Lee E.
author_sort Rössert, Christian
collection PubMed
description Intrinsic cellular properties of neurons in culture or slices are usually studied by the whole cell clamp method using low-resistant patch pipettes. These electrodes allow detailed analyses with standard electrophysiological methods such as current- or voltage-clamp. However, in these preparations large parts of the network and dendritic structures may be removed, thus preventing an adequate study of synaptic signal processing. Therefore, intact in vivo preparations or isolated in vitro whole brains have been used in which intracellular recordings are usually made with sharp, high-resistant electrodes to optimize the impalement of neurons. The general non-linear resistance properties of these electrodes, however, severely limit accurate quantitative studies of membrane dynamics especially needed for precise modelling. Therefore, we have developed a frequency-domain analysis of membrane properties that uses a Piece-wise Non-linear Electrode Compensation (PNEC) method. The technique was tested in second-order vestibular neurons and abducens motoneurons of isolated frog whole brain preparations using sharp potassium chloride- or potassium acetate-filled electrodes. All recordings were performed without online electrode compensation. The properties of each electrode were determined separately after the neuronal recordings and were used in the frequency-domain analysis of the combined measurement of electrode and cell. This allowed detailed analysis of membrane properties in the frequency-domain with high-resistant electrodes and provided quantitative data that can be further used to model channel kinetics. Thus, sharp electrodes can be used for the characterization of intrinsic properties and synaptic inputs of neurons in intact brains.
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spelling pubmed-28586102010-06-25 Frequency-Domain Analysis of Intrinsic Neuronal Properties using High-Resistant Electrodes Rössert, Christian Straka, Hans Glasauer, Stefan Moore, Lee E. Front Neurosci Neuroscience Intrinsic cellular properties of neurons in culture or slices are usually studied by the whole cell clamp method using low-resistant patch pipettes. These electrodes allow detailed analyses with standard electrophysiological methods such as current- or voltage-clamp. However, in these preparations large parts of the network and dendritic structures may be removed, thus preventing an adequate study of synaptic signal processing. Therefore, intact in vivo preparations or isolated in vitro whole brains have been used in which intracellular recordings are usually made with sharp, high-resistant electrodes to optimize the impalement of neurons. The general non-linear resistance properties of these electrodes, however, severely limit accurate quantitative studies of membrane dynamics especially needed for precise modelling. Therefore, we have developed a frequency-domain analysis of membrane properties that uses a Piece-wise Non-linear Electrode Compensation (PNEC) method. The technique was tested in second-order vestibular neurons and abducens motoneurons of isolated frog whole brain preparations using sharp potassium chloride- or potassium acetate-filled electrodes. All recordings were performed without online electrode compensation. The properties of each electrode were determined separately after the neuronal recordings and were used in the frequency-domain analysis of the combined measurement of electrode and cell. This allowed detailed analysis of membrane properties in the frequency-domain with high-resistant electrodes and provided quantitative data that can be further used to model channel kinetics. Thus, sharp electrodes can be used for the characterization of intrinsic properties and synaptic inputs of neurons in intact brains. Frontiers Research Foundation 2009-08-20 /pmc/articles/PMC2858610/ /pubmed/20582288 http://dx.doi.org/10.3389/neuro.17.002.2009 Text en Copyright © 2009 Rössert, Straka, Glasauer and Moore. http://www.frontiersin.org/licenseagreement This is an open-access article subject to an exclusive license agreement between the authors and the Frontiers Research Foundation, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are credited.
spellingShingle Neuroscience
Rössert, Christian
Straka, Hans
Glasauer, Stefan
Moore, Lee E.
Frequency-Domain Analysis of Intrinsic Neuronal Properties using High-Resistant Electrodes
title Frequency-Domain Analysis of Intrinsic Neuronal Properties using High-Resistant Electrodes
title_full Frequency-Domain Analysis of Intrinsic Neuronal Properties using High-Resistant Electrodes
title_fullStr Frequency-Domain Analysis of Intrinsic Neuronal Properties using High-Resistant Electrodes
title_full_unstemmed Frequency-Domain Analysis of Intrinsic Neuronal Properties using High-Resistant Electrodes
title_short Frequency-Domain Analysis of Intrinsic Neuronal Properties using High-Resistant Electrodes
title_sort frequency-domain analysis of intrinsic neuronal properties using high-resistant electrodes
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2858610/
https://www.ncbi.nlm.nih.gov/pubmed/20582288
http://dx.doi.org/10.3389/neuro.17.002.2009
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