Abstract
Characterizing 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. Copyright © 2022 the Author(s).
| Original language | English |
|---|---|
| Article number | e2117346119 |
| Journal | PNAS: Proceedings of the National Academy of Sciences of the United States of America |
| Volume | 119 |
| Issue number | 23 |
| Online published | 1 Jun 2022 |
| DOIs | |
| Publication status | Published - 7 Jun 2022 |
| Externally published | Yes |
Funding
This work was supported by NIH BRAIN Initiative grants (1UF1NS107696 to G.M., J.Z., J.S.J.W., J.W., K.K.T., and N.J.).
Research Keywords
- hemodynamics
- in vivo imaging
- mouse brain
- two-photon fluorescence
- vasculature
Publisher's Copyright Statement
- This full text is made available under CC-BY 4.0. https://creativecommons.org/licenses/by/4.0/
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