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Escitalopram Decreases Cross-Regional Functional Connectivity within the Default-Mode Network

The default-mode network (DMN), which comprises medial frontal, temporal and parietal regions, is part of the brain’s intrinsic organization. The serotonergic (5-HT) neurotransmitter system projects to DMN regions from midbrain efferents, and manipulation of this system could thus reveal insights in...

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Autores principales: van de Ven, Vincent, Wingen, Marleen, Kuypers, Kim P. C., Ramaekers, Johannes G., Formisano, Elia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3694983/
https://www.ncbi.nlm.nih.gov/pubmed/23826388
http://dx.doi.org/10.1371/journal.pone.0068355
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author van de Ven, Vincent
Wingen, Marleen
Kuypers, Kim P. C.
Ramaekers, Johannes G.
Formisano, Elia
author_facet van de Ven, Vincent
Wingen, Marleen
Kuypers, Kim P. C.
Ramaekers, Johannes G.
Formisano, Elia
author_sort van de Ven, Vincent
collection PubMed
description The default-mode network (DMN), which comprises medial frontal, temporal and parietal regions, is part of the brain’s intrinsic organization. The serotonergic (5-HT) neurotransmitter system projects to DMN regions from midbrain efferents, and manipulation of this system could thus reveal insights into the neurobiological mechanisms of DMN functioning. Here, we investigate intrinsic functional connectivity of the DMN as a function of activity of the serotonergic system, through the administration of the selective serotonin reuptake inhibitor (SSRI) escitalopram. We quantified DMN functional connectivity using an approach based on dual-regression. Specifically, we decomposed group data of a subset of the functional time series using spatial independent component analysis, and projected the group spatial modes to the same and an independent resting state time series of individual participants. We found no effects of escitalopram on global functional connectivity of the DMN at the map-level; that is, escitalopram did not alter the global functional architecture of the DMN. However, we found that escitalopram decreased DMN regional pairwise connectivity, which included anterior and posterior cingulate cortex, hippocampal complex and lateral parietal regions. Further, regional DMN connectivity covaried with alertness ratings across participants. Our findings show that escitalopram altered intrinsic regional DMN connectivity, which suggests that the serotonergic system plays an important role in DMN connectivity and its contribution to cognition. Pharmacological challenge designs may be a useful addition to resting-state functional MRI to investigate intrinsic brain functional organization.
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spelling pubmed-36949832013-07-03 Escitalopram Decreases Cross-Regional Functional Connectivity within the Default-Mode Network van de Ven, Vincent Wingen, Marleen Kuypers, Kim P. C. Ramaekers, Johannes G. Formisano, Elia PLoS One Research Article The default-mode network (DMN), which comprises medial frontal, temporal and parietal regions, is part of the brain’s intrinsic organization. The serotonergic (5-HT) neurotransmitter system projects to DMN regions from midbrain efferents, and manipulation of this system could thus reveal insights into the neurobiological mechanisms of DMN functioning. Here, we investigate intrinsic functional connectivity of the DMN as a function of activity of the serotonergic system, through the administration of the selective serotonin reuptake inhibitor (SSRI) escitalopram. We quantified DMN functional connectivity using an approach based on dual-regression. Specifically, we decomposed group data of a subset of the functional time series using spatial independent component analysis, and projected the group spatial modes to the same and an independent resting state time series of individual participants. We found no effects of escitalopram on global functional connectivity of the DMN at the map-level; that is, escitalopram did not alter the global functional architecture of the DMN. However, we found that escitalopram decreased DMN regional pairwise connectivity, which included anterior and posterior cingulate cortex, hippocampal complex and lateral parietal regions. Further, regional DMN connectivity covaried with alertness ratings across participants. Our findings show that escitalopram altered intrinsic regional DMN connectivity, which suggests that the serotonergic system plays an important role in DMN connectivity and its contribution to cognition. Pharmacological challenge designs may be a useful addition to resting-state functional MRI to investigate intrinsic brain functional organization. Public Library of Science 2013-06-27 /pmc/articles/PMC3694983/ /pubmed/23826388 http://dx.doi.org/10.1371/journal.pone.0068355 Text en © 2013 van de ven et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
van de Ven, Vincent
Wingen, Marleen
Kuypers, Kim P. C.
Ramaekers, Johannes G.
Formisano, Elia
Escitalopram Decreases Cross-Regional Functional Connectivity within the Default-Mode Network
title Escitalopram Decreases Cross-Regional Functional Connectivity within the Default-Mode Network
title_full Escitalopram Decreases Cross-Regional Functional Connectivity within the Default-Mode Network
title_fullStr Escitalopram Decreases Cross-Regional Functional Connectivity within the Default-Mode Network
title_full_unstemmed Escitalopram Decreases Cross-Regional Functional Connectivity within the Default-Mode Network
title_short Escitalopram Decreases Cross-Regional Functional Connectivity within the Default-Mode Network
title_sort escitalopram decreases cross-regional functional connectivity within the default-mode network
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3694983/
https://www.ncbi.nlm.nih.gov/pubmed/23826388
http://dx.doi.org/10.1371/journal.pone.0068355
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