Go to The Journal of Clinical Investigation
  • About
  • Editors
  • Consulting Editors
  • For authors
  • Journal stats
  • 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
  • Journal stats
  • 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 1

Nasal CPAP adapted for use in rats functions similarly to clinical CPAP.

Options: View larger image (or click on image) Download as PowerPoint
Nasal CPAP adapted for use in rats functions similarly to clinical CPAP....
(A–D) CPAP chamber and nose cone. (E) Overview of experiments. (F) Graph with arterial oxygenation values (PaO2) in rats breathing via the nose cone (n = 6, black dots) and CPAP (n = 5, pink dots). Each dot represents values from 1 rat. Data are shown as mean ± SEM. A linear mixed model with fixed effects of time (blood draw time), group (no CPAP vs. CPAP), and the interaction between time and group. *P = 0.029, **P = 0.028, ***P < 0.001. (G) Corresponding graph with arterial carbon dioxide (PaCO2) values. (H) Overview of experimental design for lung studies. The inhalation and exhalation phases are indicated with a red and green arrow, respectively. Black arrows indicate respiratory triggers. FLASH, fast low angle shot sequence. (I and J) Anatomical MRIs in the midbrain sagittal-view plane, which captures the upper airway anatomy including the tongue, epiglottis, and trachea. Arrows represent distance from the cavernous sinus (CS, white arrow) to the base of the tongue in a rat breathing via the nose cone (green arrow, distance = 1.6 mm) and with CPAP (pink arrow, distance = 2.6 mm). Scale bar = 3 mm. (K and L) Outline of the lungs at end expiration (functional residual capacity, FRC) without (green contour) or with CPAP (pink contour). (M and N) Corresponding MRI images acquired at peak inspiration with and without CPAP. The arrow in K points to the stomach. Scale bars = 500 μm. (O) Graph with values of FRC and inspiratory lung volumes from 6 rats where the rats served as their own controls, obtained with no CPAP (green bars) and with CPAP (pink bars). Data are mean ± SEM. A linear mixed models with fixed effects of time (respiratory cycle, i.e., end expiration and inspiration), group (no CPAP vs. CPAP), and the interaction between respiratory cycle and group. **P = 0.003, ***P = 0.001, ****P < 0.001.

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

Sign up for email alerts