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Mechanically manipulating glymphatic transport by ultrasound combined with microbubbles

The glymphatic system is a perivascular fluid transport system for waste clearance. Glymphatic transport is believed to be driven by the perivascular pumping effect created by the pulsation of the arterial wall caused by the cardiac cycle. Ultrasound sonication of circulating microbubbles (MBs) in t...

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Autores principales: Ye, Dezhuang, Chen, Si, Liu, Yajie, Weixel, Charlotte, Hu, Zhongtao, Yuan, Jinyun, Chen, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10214201/
https://www.ncbi.nlm.nih.gov/pubmed/37186852
http://dx.doi.org/10.1073/pnas.2212933120
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author Ye, Dezhuang
Chen, Si
Liu, Yajie
Weixel, Charlotte
Hu, Zhongtao
Yuan, Jinyun
Chen, Hong
author_facet Ye, Dezhuang
Chen, Si
Liu, Yajie
Weixel, Charlotte
Hu, Zhongtao
Yuan, Jinyun
Chen, Hong
author_sort Ye, Dezhuang
collection PubMed
description The glymphatic system is a perivascular fluid transport system for waste clearance. Glymphatic transport is believed to be driven by the perivascular pumping effect created by the pulsation of the arterial wall caused by the cardiac cycle. Ultrasound sonication of circulating microbubbles (MBs) in the cerebral vasculature induces volumetric expansion and contraction of MBs that push and pull on the vessel wall to generate a MB pumping effect. The objective of this study was to evaluate whether glymphatic transport can be mechanically manipulated by focused ultrasound (FUS) sonication of MBs. The glymphatic pathway in intact mouse brains was studied using intranasal administration of fluorescently labeled albumin as fluid tracers, followed by FUS sonication at a deep brain target (thalamus) in the presence of intravenously injected MBs. Intracisternal magna injection, the conventional technique used in studying glymphatic transport, was employed to provide a comparative reference. Three-dimensional confocal microscopy imaging of optically cleared brain tissue revealed that FUS sonication enhanced the transport of fluorescently labeled albumin tracer in the perivascular space (PVS) along microvessels, primarily the arterioles. We also obtained evidence of FUS-enhanced penetration of the albumin tracer from the PVS into the interstitial space. This study revealed that ultrasound combined with circulating MBs could mechanically enhance glymphatic transport in the brain.
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spelling pubmed-102142012023-05-27 Mechanically manipulating glymphatic transport by ultrasound combined with microbubbles Ye, Dezhuang Chen, Si Liu, Yajie Weixel, Charlotte Hu, Zhongtao Yuan, Jinyun Chen, Hong Proc Natl Acad Sci U S A Biological Sciences The glymphatic system is a perivascular fluid transport system for waste clearance. Glymphatic transport is believed to be driven by the perivascular pumping effect created by the pulsation of the arterial wall caused by the cardiac cycle. Ultrasound sonication of circulating microbubbles (MBs) in the cerebral vasculature induces volumetric expansion and contraction of MBs that push and pull on the vessel wall to generate a MB pumping effect. The objective of this study was to evaluate whether glymphatic transport can be mechanically manipulated by focused ultrasound (FUS) sonication of MBs. The glymphatic pathway in intact mouse brains was studied using intranasal administration of fluorescently labeled albumin as fluid tracers, followed by FUS sonication at a deep brain target (thalamus) in the presence of intravenously injected MBs. Intracisternal magna injection, the conventional technique used in studying glymphatic transport, was employed to provide a comparative reference. Three-dimensional confocal microscopy imaging of optically cleared brain tissue revealed that FUS sonication enhanced the transport of fluorescently labeled albumin tracer in the perivascular space (PVS) along microvessels, primarily the arterioles. We also obtained evidence of FUS-enhanced penetration of the albumin tracer from the PVS into the interstitial space. This study revealed that ultrasound combined with circulating MBs could mechanically enhance glymphatic transport in the brain. National Academy of Sciences 2023-05-15 2023-05-23 /pmc/articles/PMC10214201/ /pubmed/37186852 http://dx.doi.org/10.1073/pnas.2212933120 Text en Copyright © 2023 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Ye, Dezhuang
Chen, Si
Liu, Yajie
Weixel, Charlotte
Hu, Zhongtao
Yuan, Jinyun
Chen, Hong
Mechanically manipulating glymphatic transport by ultrasound combined with microbubbles
title Mechanically manipulating glymphatic transport by ultrasound combined with microbubbles
title_full Mechanically manipulating glymphatic transport by ultrasound combined with microbubbles
title_fullStr Mechanically manipulating glymphatic transport by ultrasound combined with microbubbles
title_full_unstemmed Mechanically manipulating glymphatic transport by ultrasound combined with microbubbles
title_short Mechanically manipulating glymphatic transport by ultrasound combined with microbubbles
title_sort mechanically manipulating glymphatic transport by ultrasound combined with microbubbles
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10214201/
https://www.ncbi.nlm.nih.gov/pubmed/37186852
http://dx.doi.org/10.1073/pnas.2212933120
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