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Recovery cycle times of inferior colliculus neurons in the awake bat measured with spike counts and latencies

Neural responses in the mammalian auditory midbrain (inferior colliculus; IC) arise from complex interactions of synaptic excitation, inhibition, and intrinsic properties of the cell. Temporally selective duration-tuned neurons (DTNs) in the IC are hypothesized to arise through the convergence of ex...

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Autores principales: Sayegh, Riziq, Aubie, Brandon, Fazel-Pour, Siavosh, Faure, Paul A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3422732/
https://www.ncbi.nlm.nih.gov/pubmed/22933992
http://dx.doi.org/10.3389/fncir.2012.00056
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author Sayegh, Riziq
Aubie, Brandon
Fazel-Pour, Siavosh
Faure, Paul A.
author_facet Sayegh, Riziq
Aubie, Brandon
Fazel-Pour, Siavosh
Faure, Paul A.
author_sort Sayegh, Riziq
collection PubMed
description Neural responses in the mammalian auditory midbrain (inferior colliculus; IC) arise from complex interactions of synaptic excitation, inhibition, and intrinsic properties of the cell. Temporally selective duration-tuned neurons (DTNs) in the IC are hypothesized to arise through the convergence of excitatory and inhibitory synaptic inputs offset in time. Synaptic inhibition can be inferred from extracellular recordings by presenting pairs of pulses (paired tone stimulation) and comparing the evoked responses of the cell to each pulse. We obtained single unit recordings from the IC of the awake big brown bat (Eptesicus fuscus) and used paired tone stimulation to measure the recovery cycle times of DTNs and non-temporally selective auditory neurons. By systematically varying the interpulse interval (IPI) of the paired tone stimulus, we determined the minimum IPI required for a neuron's spike count or its spike latency (first- or last-spike latency) in response to the second tone to recover to within ≥50% of the cell's baseline count or to within 1 SD of it's baseline latency in response to the first tone. Recovery times of shortpass DTNs were significantly shorter than those of bandpass DTNs, and recovery times of bandpass DTNs were longer than allpass neurons not selective for stimulus duration. Recovery times measured with spike counts were positively correlated with those measured with spike latencies. Recovery times were also correlated with first-spike latency (FSL). These findings, combined with previous studies on duration tuning in the IC, suggest that persistent inhibition is a defining characteristic of DTNs. Herein, we discuss measuring recovery times of neurons with spike counts and latencies. We also highlight how persistent inhibition could determine neural recovery times and serve as a potential mechanism underlying the precedence effect in humans. Finally, we explore implications of recovery times for DTNs in the context of bat hearing and echolocation.
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spelling pubmed-34227322012-08-29 Recovery cycle times of inferior colliculus neurons in the awake bat measured with spike counts and latencies Sayegh, Riziq Aubie, Brandon Fazel-Pour, Siavosh Faure, Paul A. Front Neural Circuits Neuroscience Neural responses in the mammalian auditory midbrain (inferior colliculus; IC) arise from complex interactions of synaptic excitation, inhibition, and intrinsic properties of the cell. Temporally selective duration-tuned neurons (DTNs) in the IC are hypothesized to arise through the convergence of excitatory and inhibitory synaptic inputs offset in time. Synaptic inhibition can be inferred from extracellular recordings by presenting pairs of pulses (paired tone stimulation) and comparing the evoked responses of the cell to each pulse. We obtained single unit recordings from the IC of the awake big brown bat (Eptesicus fuscus) and used paired tone stimulation to measure the recovery cycle times of DTNs and non-temporally selective auditory neurons. By systematically varying the interpulse interval (IPI) of the paired tone stimulus, we determined the minimum IPI required for a neuron's spike count or its spike latency (first- or last-spike latency) in response to the second tone to recover to within ≥50% of the cell's baseline count or to within 1 SD of it's baseline latency in response to the first tone. Recovery times of shortpass DTNs were significantly shorter than those of bandpass DTNs, and recovery times of bandpass DTNs were longer than allpass neurons not selective for stimulus duration. Recovery times measured with spike counts were positively correlated with those measured with spike latencies. Recovery times were also correlated with first-spike latency (FSL). These findings, combined with previous studies on duration tuning in the IC, suggest that persistent inhibition is a defining characteristic of DTNs. Herein, we discuss measuring recovery times of neurons with spike counts and latencies. We also highlight how persistent inhibition could determine neural recovery times and serve as a potential mechanism underlying the precedence effect in humans. Finally, we explore implications of recovery times for DTNs in the context of bat hearing and echolocation. Frontiers Media S.A. 2012-08-20 /pmc/articles/PMC3422732/ /pubmed/22933992 http://dx.doi.org/10.3389/fncir.2012.00056 Text en Copyright © 2012 Sayegh, Aubie, Fazel-Pour and Faure. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Neuroscience
Sayegh, Riziq
Aubie, Brandon
Fazel-Pour, Siavosh
Faure, Paul A.
Recovery cycle times of inferior colliculus neurons in the awake bat measured with spike counts and latencies
title Recovery cycle times of inferior colliculus neurons in the awake bat measured with spike counts and latencies
title_full Recovery cycle times of inferior colliculus neurons in the awake bat measured with spike counts and latencies
title_fullStr Recovery cycle times of inferior colliculus neurons in the awake bat measured with spike counts and latencies
title_full_unstemmed Recovery cycle times of inferior colliculus neurons in the awake bat measured with spike counts and latencies
title_short Recovery cycle times of inferior colliculus neurons in the awake bat measured with spike counts and latencies
title_sort recovery cycle times of inferior colliculus neurons in the awake bat measured with spike counts and latencies
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3422732/
https://www.ncbi.nlm.nih.gov/pubmed/22933992
http://dx.doi.org/10.3389/fncir.2012.00056
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