Go to The Journal of Clinical Investigation
  • About
  • Editors
  • Consulting Editors
  • For authors
  • Publication ethics
  • Publication alerts by email
  • Transfers
  • Advertising
  • Job board
  • Contact
  • Physician-Scientist Development
  • Current issue
  • Past issues
  • By specialty
    • COVID-19
    • Cardiology
    • Immunology
    • Metabolism
    • Nephrology
    • Oncology
    • Pulmonology
    • All ...
  • Videos
  • Collections
    • In-Press Preview
    • Resource and Technical Advances
    • Clinical Research and Public Health
    • Research Letters
    • Editorials
    • Perspectives
    • Physician-Scientist Development
    • Reviews
    • Top read articles

  • Current issue
  • Past issues
  • Specialties
  • In-Press Preview
  • Resource and Technical Advances
  • Clinical Research and Public Health
  • Research Letters
  • Editorials
  • Perspectives
  • Physician-Scientist Development
  • Reviews
  • Top read articles
  • About
  • Editors
  • Consulting Editors
  • For authors
  • Publication ethics
  • Publication alerts by email
  • Transfers
  • Advertising
  • Job board
  • Contact
Continuous positive airway pressure increases CSF flow and glymphatic transport
Burhan Ozturk, Sunil Koundal, Ehab Al Bizri, Xinan Chen, Zachary Gursky, Feng Dai, Andrew Lim, Paul Heerdt, Jonathan Kipnis, Allen Tannenbaum, Hedok Lee, Helene Benveniste
Burhan Ozturk, Sunil Koundal, Ehab Al Bizri, Xinan Chen, Zachary Gursky, Feng Dai, Andrew Lim, Paul Heerdt, Jonathan Kipnis, Allen Tannenbaum, Hedok Lee, Helene Benveniste
View: Text | PDF
Research Article Neuroscience

Continuous positive airway pressure increases CSF flow and glymphatic transport

  • Text
  • PDF
Abstract

Respiration can positively influence cerebrospinal fluid (CSF) flow in the brain, yet its effects on central nervous system (CNS) fluid homeostasis, including waste clearance function via glymphatic and meningeal lymphatic systems, remain unclear. Here, we investigated the effect of supporting respiratory function via continuous positive airway pressure (CPAP) on glymphatic-lymphatic function in spontaneously breathing anesthetized rodents. To do this, we used a systems approach combining engineering, MRI, computational fluid dynamics analysis, and physiological testing. We first designed a nasal CPAP device for use in the rat and demonstrated that it functioned similarly to clinical devices, as evidenced by its ability to open the upper airway, augment end-expiratory lung volume, and improve arterial oxygenation. We further showed that CPAP increased CSF flow speed at the skull base and augmented glymphatic transport regionally. The CPAP-induced augmented CSF flow speed was associated with an increase in intracranial pressure (ICP), including the ICP waveform pulse amplitude. We suggest that the augmented pulse amplitude with CPAP underlies the increase in CSF bulk flow and glymphatic transport. Our results provide insights into the functional crosstalk at the pulmonary-CSF interface and suggest that CPAP might have therapeutic benefit for sustaining glymphatic-lymphatic function.

Authors

Burhan Ozturk, Sunil Koundal, Ehab Al Bizri, Xinan Chen, Zachary Gursky, Feng Dai, Andrew Lim, Paul Heerdt, Jonathan Kipnis, Allen Tannenbaum, Hedok Lee, Helene Benveniste

×

Figure 4

CPAP sustains drainage to the cervical lymph nodes.

Options: View larger image (or click on image) Download as PowerPoint
CPAP sustains drainage to the cervical lymph nodes.
(A) Illustration of ...
(A) Illustration of the radiofrequency (RF) surface coil positioned above the neck of the rat in supine position while breathing with CPAP. (B) Anatomical MRI image at the level of the deep cervical lymph nodes (dcLN, white boxes) overlaid with corresponding solute drainage map represented by color coded signal intensity normalized to the CSF signal and time-averaged over approximately 2 hours. Scale bars = 2.5 mm. Trach, trachea; CCA, common carotid artery. (C) Time signal curves of tracer uptake in dcLNs (shown in black), accessory lymph nodes (green), and submandibular lymph nodes (blue) from a normal rat. (D) Volumes of the dcLNs extracted from rats breathing via the nose cone (gray bar) or CPAP set at 3 cmH2O (pink bar). Each dot above the bars represents values from 1 dcLN with 2 dcLNs/rat. Data are mean ± SEM. An independent 2-sided t test was used and revealed no differences in dcLN volume across the 2 groups (P = 0.2016). (E) Time signal curves (TSC) from the dcLNs of each rat derived from independent experiments of n = 6 rats breathing via the nose cone. Each line represents average signal change of the right- or left-sided dcLNs from each rat. (F) Corresponding TSC data extracted from dcLNs derived from independent experiments of n = 5 rats breathing with CPAP set at 3 cmH2O.

Copyright © 2026 American Society for Clinical Investigation
ISSN 2379-3708

Sign up for email alerts