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Transport pathways and kinetics of cerebrospinal fluid tracers in mouse brain observed by dynamic contrast-enhanced MRI

Recent studies have suggested the glymphatic system as a key mechanism of waste removal in the brain. Dynamic contrast-enhanced MRI (DCE-MRI) using intracisternally administered contrast agents is a promising tool for assessing glymphatic function in the whole brain. In this study, we evaluated the...

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Autores principales: Zhu, Yuran, Wang, Guanhua, Kolluru, Chaitanya, Gu, Yuning, Gao, Huiyun, Zhang, Jing, Wang, Yunmei, Wilson, David L., Zhu, Xiaofeng, Flask, Chris A., Yu, Xin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10449788/
https://www.ncbi.nlm.nih.gov/pubmed/37620371
http://dx.doi.org/10.1038/s41598-023-40896-x
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author Zhu, Yuran
Wang, Guanhua
Kolluru, Chaitanya
Gu, Yuning
Gao, Huiyun
Zhang, Jing
Wang, Yunmei
Wilson, David L.
Zhu, Xiaofeng
Flask, Chris A.
Yu, Xin
author_facet Zhu, Yuran
Wang, Guanhua
Kolluru, Chaitanya
Gu, Yuning
Gao, Huiyun
Zhang, Jing
Wang, Yunmei
Wilson, David L.
Zhu, Xiaofeng
Flask, Chris A.
Yu, Xin
author_sort Zhu, Yuran
collection PubMed
description Recent studies have suggested the glymphatic system as a key mechanism of waste removal in the brain. Dynamic contrast-enhanced MRI (DCE-MRI) using intracisternally administered contrast agents is a promising tool for assessing glymphatic function in the whole brain. In this study, we evaluated the transport kinetics and distribution of three MRI contrast agents with vastly different molecular sizes in mice. Our results demonstrate that oxygen-17 enriched water (H(2)(17)O), which has direct access to parenchymal tissues via aquaporin-4 water channels, exhibited significantly faster and more extensive transport compared to the two gadolinium-based contrast agents (Gd-DTPA and GadoSpin). Time-lagged correlation and clustering analyses also revealed different transport pathways for Gd-DTPA and H(2)(17)O. Furthermore, there were significant differences in transport kinetics of the three contrast agents to the lateral ventricles, reflecting the differences in forces that drive solute transport in the brain. These findings suggest the size-dependent transport pathways and kinetics of intracisternally administered contrast agents and the potential of DCE-MRI for assessing multiple aspects of solute transport in the glymphatic system.
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spelling pubmed-104497882023-08-26 Transport pathways and kinetics of cerebrospinal fluid tracers in mouse brain observed by dynamic contrast-enhanced MRI Zhu, Yuran Wang, Guanhua Kolluru, Chaitanya Gu, Yuning Gao, Huiyun Zhang, Jing Wang, Yunmei Wilson, David L. Zhu, Xiaofeng Flask, Chris A. Yu, Xin Sci Rep Article Recent studies have suggested the glymphatic system as a key mechanism of waste removal in the brain. Dynamic contrast-enhanced MRI (DCE-MRI) using intracisternally administered contrast agents is a promising tool for assessing glymphatic function in the whole brain. In this study, we evaluated the transport kinetics and distribution of three MRI contrast agents with vastly different molecular sizes in mice. Our results demonstrate that oxygen-17 enriched water (H(2)(17)O), which has direct access to parenchymal tissues via aquaporin-4 water channels, exhibited significantly faster and more extensive transport compared to the two gadolinium-based contrast agents (Gd-DTPA and GadoSpin). Time-lagged correlation and clustering analyses also revealed different transport pathways for Gd-DTPA and H(2)(17)O. Furthermore, there were significant differences in transport kinetics of the three contrast agents to the lateral ventricles, reflecting the differences in forces that drive solute transport in the brain. These findings suggest the size-dependent transport pathways and kinetics of intracisternally administered contrast agents and the potential of DCE-MRI for assessing multiple aspects of solute transport in the glymphatic system. Nature Publishing Group UK 2023-08-24 /pmc/articles/PMC10449788/ /pubmed/37620371 http://dx.doi.org/10.1038/s41598-023-40896-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Zhu, Yuran
Wang, Guanhua
Kolluru, Chaitanya
Gu, Yuning
Gao, Huiyun
Zhang, Jing
Wang, Yunmei
Wilson, David L.
Zhu, Xiaofeng
Flask, Chris A.
Yu, Xin
Transport pathways and kinetics of cerebrospinal fluid tracers in mouse brain observed by dynamic contrast-enhanced MRI
title Transport pathways and kinetics of cerebrospinal fluid tracers in mouse brain observed by dynamic contrast-enhanced MRI
title_full Transport pathways and kinetics of cerebrospinal fluid tracers in mouse brain observed by dynamic contrast-enhanced MRI
title_fullStr Transport pathways and kinetics of cerebrospinal fluid tracers in mouse brain observed by dynamic contrast-enhanced MRI
title_full_unstemmed Transport pathways and kinetics of cerebrospinal fluid tracers in mouse brain observed by dynamic contrast-enhanced MRI
title_short Transport pathways and kinetics of cerebrospinal fluid tracers in mouse brain observed by dynamic contrast-enhanced MRI
title_sort transport pathways and kinetics of cerebrospinal fluid tracers in mouse brain observed by dynamic contrast-enhanced mri
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10449788/
https://www.ncbi.nlm.nih.gov/pubmed/37620371
http://dx.doi.org/10.1038/s41598-023-40896-x
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