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Control of the neurovascular coupling by nitric oxide-dependent regulation of astrocytic Ca(2+) signaling

Neuronal activity must be tightly coordinated with blood flow to keep proper brain function, which is achieved by a mechanism known as neurovascular coupling. Then, an increase in synaptic activity leads to a dilation of local parenchymal arterioles that matches the enhanced metabolic demand. Neurov...

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Autores principales: Muñoz, Manuel F., Puebla, Mariela, Figueroa, Xavier F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4354411/
https://www.ncbi.nlm.nih.gov/pubmed/25805969
http://dx.doi.org/10.3389/fncel.2015.00059
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author Muñoz, Manuel F.
Puebla, Mariela
Figueroa, Xavier F.
author_facet Muñoz, Manuel F.
Puebla, Mariela
Figueroa, Xavier F.
author_sort Muñoz, Manuel F.
collection PubMed
description Neuronal activity must be tightly coordinated with blood flow to keep proper brain function, which is achieved by a mechanism known as neurovascular coupling. Then, an increase in synaptic activity leads to a dilation of local parenchymal arterioles that matches the enhanced metabolic demand. Neurovascular coupling is orchestrated by astrocytes. These glial cells are located between neurons and the microvasculature, with the astrocytic endfeet ensheathing the vessels, which allows fine intercellular communication. The neurotransmitters released during neuronal activity reach astrocytic receptors and trigger a Ca(2+) signaling that propagates to the endfeet, activating the release of vasoactive factors and arteriolar dilation. The astrocyte Ca(2+) signaling is coordinated by gap junction channels and hemichannels formed by connexins (Cx43 and Cx30) and channels formed by pannexins (Panx-1). The neuronal activity-initiated Ca(2+) waves are propagated among neighboring astrocytes directly via gap junctions or through ATP release via connexin hemichannels or pannexin channels. In addition, Ca(2+) entry via connexin hemichannels or pannexin channels may participate in the regulation of the astrocyte signaling-mediated neurovascular coupling. Interestingly, nitric oxide (NO) can activate connexin hemichannel by S-nitrosylation and the Ca(2+)-dependent NO-synthesizing enzymes endothelial NO synthase (eNOS) and neuronal NOS (nNOS) are expressed in astrocytes. Therefore, the astrocytic Ca(2+) signaling triggered in neurovascular coupling may activate NO production, which, in turn, may lead to Ca(2+) influx through hemichannel activation. Furthermore, NO release from the hemichannels located at astrocytic endfeet may contribute to the vasodilation of parenchymal arterioles. In this review, we discuss the mechanisms involved in the regulation of the astrocytic Ca(2+) signaling that mediates neurovascular coupling, with a special emphasis in the possible participation of NO in this process.
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spelling pubmed-43544112015-03-24 Control of the neurovascular coupling by nitric oxide-dependent regulation of astrocytic Ca(2+) signaling Muñoz, Manuel F. Puebla, Mariela Figueroa, Xavier F. Front Cell Neurosci Neuroscience Neuronal activity must be tightly coordinated with blood flow to keep proper brain function, which is achieved by a mechanism known as neurovascular coupling. Then, an increase in synaptic activity leads to a dilation of local parenchymal arterioles that matches the enhanced metabolic demand. Neurovascular coupling is orchestrated by astrocytes. These glial cells are located between neurons and the microvasculature, with the astrocytic endfeet ensheathing the vessels, which allows fine intercellular communication. The neurotransmitters released during neuronal activity reach astrocytic receptors and trigger a Ca(2+) signaling that propagates to the endfeet, activating the release of vasoactive factors and arteriolar dilation. The astrocyte Ca(2+) signaling is coordinated by gap junction channels and hemichannels formed by connexins (Cx43 and Cx30) and channels formed by pannexins (Panx-1). The neuronal activity-initiated Ca(2+) waves are propagated among neighboring astrocytes directly via gap junctions or through ATP release via connexin hemichannels or pannexin channels. In addition, Ca(2+) entry via connexin hemichannels or pannexin channels may participate in the regulation of the astrocyte signaling-mediated neurovascular coupling. Interestingly, nitric oxide (NO) can activate connexin hemichannel by S-nitrosylation and the Ca(2+)-dependent NO-synthesizing enzymes endothelial NO synthase (eNOS) and neuronal NOS (nNOS) are expressed in astrocytes. Therefore, the astrocytic Ca(2+) signaling triggered in neurovascular coupling may activate NO production, which, in turn, may lead to Ca(2+) influx through hemichannel activation. Furthermore, NO release from the hemichannels located at astrocytic endfeet may contribute to the vasodilation of parenchymal arterioles. In this review, we discuss the mechanisms involved in the regulation of the astrocytic Ca(2+) signaling that mediates neurovascular coupling, with a special emphasis in the possible participation of NO in this process. Frontiers Media S.A. 2015-03-10 /pmc/articles/PMC4354411/ /pubmed/25805969 http://dx.doi.org/10.3389/fncel.2015.00059 Text en Copyright © 2015 Muñoz, Puebla and Figueroa. http://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 and reproduction in other forums is permitted, provided the original author(s) or licensor 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
Muñoz, Manuel F.
Puebla, Mariela
Figueroa, Xavier F.
Control of the neurovascular coupling by nitric oxide-dependent regulation of astrocytic Ca(2+) signaling
title Control of the neurovascular coupling by nitric oxide-dependent regulation of astrocytic Ca(2+) signaling
title_full Control of the neurovascular coupling by nitric oxide-dependent regulation of astrocytic Ca(2+) signaling
title_fullStr Control of the neurovascular coupling by nitric oxide-dependent regulation of astrocytic Ca(2+) signaling
title_full_unstemmed Control of the neurovascular coupling by nitric oxide-dependent regulation of astrocytic Ca(2+) signaling
title_short Control of the neurovascular coupling by nitric oxide-dependent regulation of astrocytic Ca(2+) signaling
title_sort control of the neurovascular coupling by nitric oxide-dependent regulation of astrocytic ca(2+) signaling
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4354411/
https://www.ncbi.nlm.nih.gov/pubmed/25805969
http://dx.doi.org/10.3389/fncel.2015.00059
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