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Article: Ultrafast two-photon fluorescence imaging of cerebral blood circulation in the mouse brain in vivo

TitleUltrafast two-photon fluorescence imaging of cerebral blood circulation in the mouse brain in vivo
Authors
Keywordshemodynamics
in vivo imaging
mouse brain
two-photon fluorescence
vasculature
Issue Date7-Jun-2022
PublisherNational Academy of Sciences
Citation
Proceedings of the National Academy of Sciences, 2022, v. 119, n. 23 How to Cite?
AbstractCharacterizing blood flow dynamics in vivo is critical to understanding the function of the vascular network under physiological and pathological conditions. Existing methods for hemodynamic imaging have insufficient spatial and temporal resolution to monitor blood flow at the cellular level in large blood vessels. By using an ultrafast line-scanning module based on free-space angular chirped enhanced delay, we achieved two-photon fluorescence imaging of cortical blood flow at 1,000 two-dimensional (2D) frames and 1,000,000 one-dimensional line scans per second in the awake mouse. This orders-of-magnitude increase in temporal resolution allowed us to measure cerebral blood flow at up to 49 mm/s and observe pulsatile blood flow at harmonics of heart rate. Directly visualizing red blood cell (RBC) flow through vessels down to >800 μm in depth, we characterized cortical layer–dependent flow velocity distributions of capillaries, obtained radial velocity profiles and kilohertz 2D velocity mapping of multifile blood flow, and performed RBC flux measurements from penetrating blood vessels.
Persistent Identifierhttp://hdl.handle.net/10722/338898
ISSN
2023 Impact Factor: 9.4
2023 SCImago Journal Rankings: 3.737
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorMeng, G-
dc.contributor.authorZhong, J-
dc.contributor.authorZhang, Q-
dc.contributor.authorWong, JSJ-
dc.contributor.authorWu, J-
dc.contributor.authorTsia, KK-
dc.contributor.authorJi, N-
dc.date.accessioned2024-03-11T10:32:21Z-
dc.date.available2024-03-11T10:32:21Z-
dc.date.issued2022-06-07-
dc.identifier.citationProceedings of the National Academy of Sciences, 2022, v. 119, n. 23-
dc.identifier.issn0027-8424-
dc.identifier.urihttp://hdl.handle.net/10722/338898-
dc.description.abstractCharacterizing blood flow dynamics in vivo is critical to understanding the function of the vascular network under physiological and pathological conditions. Existing methods for hemodynamic imaging have insufficient spatial and temporal resolution to monitor blood flow at the cellular level in large blood vessels. By using an ultrafast line-scanning module based on free-space angular chirped enhanced delay, we achieved two-photon fluorescence imaging of cortical blood flow at 1,000 two-dimensional (2D) frames and 1,000,000 one-dimensional line scans per second in the awake mouse. This orders-of-magnitude increase in temporal resolution allowed us to measure cerebral blood flow at up to 49 mm/s and observe pulsatile blood flow at harmonics of heart rate. Directly visualizing red blood cell (RBC) flow through vessels down to >800 μm in depth, we characterized cortical layer–dependent flow velocity distributions of capillaries, obtained radial velocity profiles and kilohertz 2D velocity mapping of multifile blood flow, and performed RBC flux measurements from penetrating blood vessels.-
dc.languageeng-
dc.publisherNational Academy of Sciences-
dc.relation.ispartofProceedings of the National Academy of Sciences-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjecthemodynamics-
dc.subjectin vivo imaging-
dc.subjectmouse brain-
dc.subjecttwo-photon fluorescence-
dc.subjectvasculature-
dc.titleUltrafast two-photon fluorescence imaging of cerebral blood circulation in the mouse brain in vivo-
dc.typeArticle-
dc.identifier.doi10.1073/pnas.2117346119-
dc.identifier.scopuseid_2-s2.0-85131270950-
dc.identifier.volume119-
dc.identifier.issue23-
dc.identifier.eissn1091-6490-
dc.identifier.isiWOS:001051458200003-
dc.identifier.issnl0027-8424-

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