Dysregulation of excitatory neural firing replicates physiological and functional changes in aging visual cortex.

The mammalian visual system has been the focus of countless experimental and theoretical studies designed to elucidate principles of neural computation and sensory coding. Most theoretical work has focused on networks intended to reflect developing or mature neural circuitry, in both health and dise...

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Main Authors: Seth Talyansky, Braden A W Brinkman
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2021-01-01
Series:PLoS Computational Biology
Online Access:https://doi.org/10.1371/journal.pcbi.1008620
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spelling doaj-72bf1a61facf4589bef5db9ff182fcd12021-05-19T04:31:39ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582021-01-01171e100862010.1371/journal.pcbi.1008620Dysregulation of excitatory neural firing replicates physiological and functional changes in aging visual cortex.Seth TalyanskyBraden A W BrinkmanThe mammalian visual system has been the focus of countless experimental and theoretical studies designed to elucidate principles of neural computation and sensory coding. Most theoretical work has focused on networks intended to reflect developing or mature neural circuitry, in both health and disease. Few computational studies have attempted to model changes that occur in neural circuitry as an organism ages non-pathologically. In this work we contribute to closing this gap, studying how physiological changes correlated with advanced age impact the computational performance of a spiking network model of primary visual cortex (V1). Our results demonstrate that deterioration of homeostatic regulation of excitatory firing, coupled with long-term synaptic plasticity, is a sufficient mechanism to reproduce features of observed physiological and functional changes in neural activity data, specifically declines in inhibition and in selectivity to oriented stimuli. This suggests a potential causality between dysregulation of neuron firing and age-induced changes in brain physiology and functional performance. While this does not rule out deeper underlying causes or other mechanisms that could give rise to these changes, our approach opens new avenues for exploring these underlying mechanisms in greater depth and making predictions for future experiments.https://doi.org/10.1371/journal.pcbi.1008620
collection DOAJ
language English
format Article
sources DOAJ
author Seth Talyansky
Braden A W Brinkman
spellingShingle Seth Talyansky
Braden A W Brinkman
Dysregulation of excitatory neural firing replicates physiological and functional changes in aging visual cortex.
PLoS Computational Biology
author_facet Seth Talyansky
Braden A W Brinkman
author_sort Seth Talyansky
title Dysregulation of excitatory neural firing replicates physiological and functional changes in aging visual cortex.
title_short Dysregulation of excitatory neural firing replicates physiological and functional changes in aging visual cortex.
title_full Dysregulation of excitatory neural firing replicates physiological and functional changes in aging visual cortex.
title_fullStr Dysregulation of excitatory neural firing replicates physiological and functional changes in aging visual cortex.
title_full_unstemmed Dysregulation of excitatory neural firing replicates physiological and functional changes in aging visual cortex.
title_sort dysregulation of excitatory neural firing replicates physiological and functional changes in aging visual cortex.
publisher Public Library of Science (PLoS)
series PLoS Computational Biology
issn 1553-734X
1553-7358
publishDate 2021-01-01
description The mammalian visual system has been the focus of countless experimental and theoretical studies designed to elucidate principles of neural computation and sensory coding. Most theoretical work has focused on networks intended to reflect developing or mature neural circuitry, in both health and disease. Few computational studies have attempted to model changes that occur in neural circuitry as an organism ages non-pathologically. In this work we contribute to closing this gap, studying how physiological changes correlated with advanced age impact the computational performance of a spiking network model of primary visual cortex (V1). Our results demonstrate that deterioration of homeostatic regulation of excitatory firing, coupled with long-term synaptic plasticity, is a sufficient mechanism to reproduce features of observed physiological and functional changes in neural activity data, specifically declines in inhibition and in selectivity to oriented stimuli. This suggests a potential causality between dysregulation of neuron firing and age-induced changes in brain physiology and functional performance. While this does not rule out deeper underlying causes or other mechanisms that could give rise to these changes, our approach opens new avenues for exploring these underlying mechanisms in greater depth and making predictions for future experiments.
url https://doi.org/10.1371/journal.pcbi.1008620
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