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Spontaneous Infraslow Fluctuations Modulate Hippocampal EPSP-PS Coupling

Extensive trial-to-trial variability is a hallmark of most behavioral, cognitive, and physiological processes. Spontaneous brain activity (SBA), a ubiquitous phenomenon that coordinates levels and patterns of neuronal activity throughout the brain, may contribute to this variability by dynamically a...

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Autores principales: Dash, Michael B., Ajayi, Stephen, Folsom, Lynde, Gold, Paul E., Korol, Donna L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5771682/
https://www.ncbi.nlm.nih.gov/pubmed/29349291
http://dx.doi.org/10.1523/ENEURO.0403-17.2017
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author Dash, Michael B.
Ajayi, Stephen
Folsom, Lynde
Gold, Paul E.
Korol, Donna L.
author_facet Dash, Michael B.
Ajayi, Stephen
Folsom, Lynde
Gold, Paul E.
Korol, Donna L.
author_sort Dash, Michael B.
collection PubMed
description Extensive trial-to-trial variability is a hallmark of most behavioral, cognitive, and physiological processes. Spontaneous brain activity (SBA), a ubiquitous phenomenon that coordinates levels and patterns of neuronal activity throughout the brain, may contribute to this variability by dynamically altering neuronal excitability. In freely-behaving male rats, we observed extensive variability of the hippocampal evoked response across 28-min recording periods despite maintaining constant stimulation parameters of the medial perforant path. This variability was related to antecedent SBA: increases in low-frequency (0.5–9 Hz) and high-frequency (40.25–100 Hz) band-limited power (BLP) in the 4-s preceding stimulation were associated with decreased slope of the field EPSP (fEPSP) and increased population spike (PS) amplitude. These fluctuations in SBA and evoked response magnitude did not appear stochastic but rather exhibited coordinated activity across infraslow timescales (0.005–0.02 Hz). Specifically, infraslow fluctuations in high- and low-frequency BLP were antiphase with changes in fEPSP slope and in phase with changes in PS amplitude. With these divergent effects on the fEPSP and PS, infraslow SBA ultimately modulates EPSP-PS coupling and thereby enables hippocampal circuitry to generate heterogeneous outputs from identical inputs. Consequently, infraslow SBA appears well suited to dynamically alter sensory selection and information processing and highlights the fundamental role of endogenous neuronal activity for shaping the brain’s response to incoming stimuli.
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spelling pubmed-57716822018-01-18 Spontaneous Infraslow Fluctuations Modulate Hippocampal EPSP-PS Coupling Dash, Michael B. Ajayi, Stephen Folsom, Lynde Gold, Paul E. Korol, Donna L. eNeuro New Research Extensive trial-to-trial variability is a hallmark of most behavioral, cognitive, and physiological processes. Spontaneous brain activity (SBA), a ubiquitous phenomenon that coordinates levels and patterns of neuronal activity throughout the brain, may contribute to this variability by dynamically altering neuronal excitability. In freely-behaving male rats, we observed extensive variability of the hippocampal evoked response across 28-min recording periods despite maintaining constant stimulation parameters of the medial perforant path. This variability was related to antecedent SBA: increases in low-frequency (0.5–9 Hz) and high-frequency (40.25–100 Hz) band-limited power (BLP) in the 4-s preceding stimulation were associated with decreased slope of the field EPSP (fEPSP) and increased population spike (PS) amplitude. These fluctuations in SBA and evoked response magnitude did not appear stochastic but rather exhibited coordinated activity across infraslow timescales (0.005–0.02 Hz). Specifically, infraslow fluctuations in high- and low-frequency BLP were antiphase with changes in fEPSP slope and in phase with changes in PS amplitude. With these divergent effects on the fEPSP and PS, infraslow SBA ultimately modulates EPSP-PS coupling and thereby enables hippocampal circuitry to generate heterogeneous outputs from identical inputs. Consequently, infraslow SBA appears well suited to dynamically alter sensory selection and information processing and highlights the fundamental role of endogenous neuronal activity for shaping the brain’s response to incoming stimuli. Society for Neuroscience 2018-01-17 /pmc/articles/PMC5771682/ /pubmed/29349291 http://dx.doi.org/10.1523/ENEURO.0403-17.2017 Text en Copyright © 2018 Dash et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle New Research
Dash, Michael B.
Ajayi, Stephen
Folsom, Lynde
Gold, Paul E.
Korol, Donna L.
Spontaneous Infraslow Fluctuations Modulate Hippocampal EPSP-PS Coupling
title Spontaneous Infraslow Fluctuations Modulate Hippocampal EPSP-PS Coupling
title_full Spontaneous Infraslow Fluctuations Modulate Hippocampal EPSP-PS Coupling
title_fullStr Spontaneous Infraslow Fluctuations Modulate Hippocampal EPSP-PS Coupling
title_full_unstemmed Spontaneous Infraslow Fluctuations Modulate Hippocampal EPSP-PS Coupling
title_short Spontaneous Infraslow Fluctuations Modulate Hippocampal EPSP-PS Coupling
title_sort spontaneous infraslow fluctuations modulate hippocampal epsp-ps coupling
topic New Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5771682/
https://www.ncbi.nlm.nih.gov/pubmed/29349291
http://dx.doi.org/10.1523/ENEURO.0403-17.2017
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