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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Series: | PLoS Computational Biology |
Online Access: | https://doi.org/10.1371/journal.pcbi.1008620 |
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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 |
work_keys_str_mv |
AT sethtalyansky dysregulationofexcitatoryneuralfiringreplicatesphysiologicalandfunctionalchangesinagingvisualcortex AT bradenawbrinkman dysregulationofexcitatoryneuralfiringreplicatesphysiologicalandfunctionalchangesinagingvisualcortex |
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