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The Effect of Light Sedation with Midazolam on Functional Connectivity of the Dorsal Attention Network

Altered connectivity within and between the resting-state networks (RSNs) brought about by anesthetics that induce altered consciousness remains incompletely understood. It is known that the dorsal attention network (DAN) and its anticorrelations with other RSNs have been implicated in consciousness...

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Autores principales: Wang, Junkai, Xu, Yachao, Deshpande, Gopikrishna, Li, Kuncheng, Sun, Pei, Liang, Peipeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8392174/
https://www.ncbi.nlm.nih.gov/pubmed/34439725
http://dx.doi.org/10.3390/brainsci11081107
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author Wang, Junkai
Xu, Yachao
Deshpande, Gopikrishna
Li, Kuncheng
Sun, Pei
Liang, Peipeng
author_facet Wang, Junkai
Xu, Yachao
Deshpande, Gopikrishna
Li, Kuncheng
Sun, Pei
Liang, Peipeng
author_sort Wang, Junkai
collection PubMed
description Altered connectivity within and between the resting-state networks (RSNs) brought about by anesthetics that induce altered consciousness remains incompletely understood. It is known that the dorsal attention network (DAN) and its anticorrelations with other RSNs have been implicated in consciousness. However, the role of DAN-related functional patterns in drug-induced sedative effects is less clear. In the current study, we investigated altered functional connectivity of the DAN during midazolam-induced light sedation. In a placebo-controlled and within-subjects experimental study, fourteen healthy volunteers received midazolam or saline with a 1-week interval. Resting-state fMRI data were acquired before and after intravenous drug administration. A multiple region of interest-driven analysis was employed to investigate connectivity within and between RSNs. It was found that functional connectivity was significantly decreased by midazolam injection in two regions located in the left inferior parietal lobule and the left middle temporal area within the DAN as compared with the saline condition. We also identified three clusters in anticorrelation between the DAN and other RSNs for the interaction effect, which included the left medial prefrontal cortex, the right superior temporal gyrus, and the right superior frontal gyrus. Connectivity between all regions and DAN was significantly decreased by midazolam injection. The sensorimotor network was minimally affected. Midazolam decreased functional connectivity of the dorsal attention network. These findings advance the understanding of the neural mechanism of sedation, and such functional patterns might have clinical implications in other medical conditions related to patients with cognitive impairment.
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spelling pubmed-83921742021-08-28 The Effect of Light Sedation with Midazolam on Functional Connectivity of the Dorsal Attention Network Wang, Junkai Xu, Yachao Deshpande, Gopikrishna Li, Kuncheng Sun, Pei Liang, Peipeng Brain Sci Article Altered connectivity within and between the resting-state networks (RSNs) brought about by anesthetics that induce altered consciousness remains incompletely understood. It is known that the dorsal attention network (DAN) and its anticorrelations with other RSNs have been implicated in consciousness. However, the role of DAN-related functional patterns in drug-induced sedative effects is less clear. In the current study, we investigated altered functional connectivity of the DAN during midazolam-induced light sedation. In a placebo-controlled and within-subjects experimental study, fourteen healthy volunteers received midazolam or saline with a 1-week interval. Resting-state fMRI data were acquired before and after intravenous drug administration. A multiple region of interest-driven analysis was employed to investigate connectivity within and between RSNs. It was found that functional connectivity was significantly decreased by midazolam injection in two regions located in the left inferior parietal lobule and the left middle temporal area within the DAN as compared with the saline condition. We also identified three clusters in anticorrelation between the DAN and other RSNs for the interaction effect, which included the left medial prefrontal cortex, the right superior temporal gyrus, and the right superior frontal gyrus. Connectivity between all regions and DAN was significantly decreased by midazolam injection. The sensorimotor network was minimally affected. Midazolam decreased functional connectivity of the dorsal attention network. These findings advance the understanding of the neural mechanism of sedation, and such functional patterns might have clinical implications in other medical conditions related to patients with cognitive impairment. MDPI 2021-08-22 /pmc/articles/PMC8392174/ /pubmed/34439725 http://dx.doi.org/10.3390/brainsci11081107 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Wang, Junkai
Xu, Yachao
Deshpande, Gopikrishna
Li, Kuncheng
Sun, Pei
Liang, Peipeng
The Effect of Light Sedation with Midazolam on Functional Connectivity of the Dorsal Attention Network
title The Effect of Light Sedation with Midazolam on Functional Connectivity of the Dorsal Attention Network
title_full The Effect of Light Sedation with Midazolam on Functional Connectivity of the Dorsal Attention Network
title_fullStr The Effect of Light Sedation with Midazolam on Functional Connectivity of the Dorsal Attention Network
title_full_unstemmed The Effect of Light Sedation with Midazolam on Functional Connectivity of the Dorsal Attention Network
title_short The Effect of Light Sedation with Midazolam on Functional Connectivity of the Dorsal Attention Network
title_sort effect of light sedation with midazolam on functional connectivity of the dorsal attention network
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8392174/
https://www.ncbi.nlm.nih.gov/pubmed/34439725
http://dx.doi.org/10.3390/brainsci11081107
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