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A Network Architecture for Bidirectional Neurovascular Coupling in Rat Whisker Barrel Cortex

Neurovascular coupling is typically considered as a master-slave relationship between the neurons and the cerebral vessels: the neurons demand energy which the vessels supply in the form of glucose and oxygen. In the recent past, both theoretical and experimental studies have suggested that the neur...

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Autores principales: Kumar, Bhadra S., Khot, Aditi, Chakravarthy, V. Srinivasa, Pushpavanam, S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8241226/
https://www.ncbi.nlm.nih.gov/pubmed/34211384
http://dx.doi.org/10.3389/fncom.2021.638700
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author Kumar, Bhadra S.
Khot, Aditi
Chakravarthy, V. Srinivasa
Pushpavanam, S.
author_facet Kumar, Bhadra S.
Khot, Aditi
Chakravarthy, V. Srinivasa
Pushpavanam, S.
author_sort Kumar, Bhadra S.
collection PubMed
description Neurovascular coupling is typically considered as a master-slave relationship between the neurons and the cerebral vessels: the neurons demand energy which the vessels supply in the form of glucose and oxygen. In the recent past, both theoretical and experimental studies have suggested that the neurovascular coupling is a bidirectional system, a loop that includes a feedback signal from the vessels influencing neural firing and plasticity. An integrated model of bidirectionally connected neural network and the vascular network is hence required to understand the relationship between the informational and metabolic aspects of neural dynamics. In this study, we present a computational model of the bidirectional neurovascular system in the whisker barrel cortex and study the effect of such coupling on neural activity and plasticity as manifest in the whisker barrel map formation. In this model, a biologically plausible self-organizing network model of rate coded, dynamic neurons is nourished by a network of vessels modeled using the biophysical properties of blood vessels. The neural layer which is designed to simulate the whisker barrel cortex of rat transmits vasodilatory signals to the vessels. The feedback from the vessels is in the form of available oxygen for oxidative metabolism whose end result is the adenosine triphosphate (ATP) necessary to fuel neural firing. The model captures the effect of the feedback from the vascular network on the neuronal map formation in the whisker barrel model under normal and pathological (Hypoxia and Hypoxia-Ischemia) conditions.
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spelling pubmed-82412262021-06-30 A Network Architecture for Bidirectional Neurovascular Coupling in Rat Whisker Barrel Cortex Kumar, Bhadra S. Khot, Aditi Chakravarthy, V. Srinivasa Pushpavanam, S. Front Comput Neurosci Neuroscience Neurovascular coupling is typically considered as a master-slave relationship between the neurons and the cerebral vessels: the neurons demand energy which the vessels supply in the form of glucose and oxygen. In the recent past, both theoretical and experimental studies have suggested that the neurovascular coupling is a bidirectional system, a loop that includes a feedback signal from the vessels influencing neural firing and plasticity. An integrated model of bidirectionally connected neural network and the vascular network is hence required to understand the relationship between the informational and metabolic aspects of neural dynamics. In this study, we present a computational model of the bidirectional neurovascular system in the whisker barrel cortex and study the effect of such coupling on neural activity and plasticity as manifest in the whisker barrel map formation. In this model, a biologically plausible self-organizing network model of rate coded, dynamic neurons is nourished by a network of vessels modeled using the biophysical properties of blood vessels. The neural layer which is designed to simulate the whisker barrel cortex of rat transmits vasodilatory signals to the vessels. The feedback from the vessels is in the form of available oxygen for oxidative metabolism whose end result is the adenosine triphosphate (ATP) necessary to fuel neural firing. The model captures the effect of the feedback from the vascular network on the neuronal map formation in the whisker barrel model under normal and pathological (Hypoxia and Hypoxia-Ischemia) conditions. Frontiers Media S.A. 2021-06-15 /pmc/articles/PMC8241226/ /pubmed/34211384 http://dx.doi.org/10.3389/fncom.2021.638700 Text en Copyright © 2021 Kumar, Khot, Chakravarthy and Pushpavanam. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Kumar, Bhadra S.
Khot, Aditi
Chakravarthy, V. Srinivasa
Pushpavanam, S.
A Network Architecture for Bidirectional Neurovascular Coupling in Rat Whisker Barrel Cortex
title A Network Architecture for Bidirectional Neurovascular Coupling in Rat Whisker Barrel Cortex
title_full A Network Architecture for Bidirectional Neurovascular Coupling in Rat Whisker Barrel Cortex
title_fullStr A Network Architecture for Bidirectional Neurovascular Coupling in Rat Whisker Barrel Cortex
title_full_unstemmed A Network Architecture for Bidirectional Neurovascular Coupling in Rat Whisker Barrel Cortex
title_short A Network Architecture for Bidirectional Neurovascular Coupling in Rat Whisker Barrel Cortex
title_sort network architecture for bidirectional neurovascular coupling in rat whisker barrel cortex
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8241226/
https://www.ncbi.nlm.nih.gov/pubmed/34211384
http://dx.doi.org/10.3389/fncom.2021.638700
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