» Articles » PMID: 29141045

CSF in the Ventricles of the Brain Behaves As a Relay Medium for Arteriovenous Pulse Wave Phase Coupling

Overview
Journal PLoS One
Date 2017 Nov 16
PMID 29141045
Citations 9
Authors
Affiliations
Soon will be listed here.
Abstract

The ventricles of the brain remain perhaps the largest anatomic structure in the human body without established primary purpose, even though their existence has been known at least since described by Aristotle. We hypothesize that the ventricles help match a stroke volume of arterial blood that arrives into the rigid cranium with an equivalent volume of ejected venous blood by spatially configuring cerebrospinal fluid (CSF) to act as a low viscosity relay medium for arteriovenous pulse wave (PW) phase coupling. We probe the hypothesis by comparing the spatiotemporal behavior of vascular PW about the ventricular surfaces in piglets to internal observations of ventricle wall motions and adjacent CSF pressure variations in humans. With wavelet brain angiography data obtained from piglets, we map the travel relative to brain pulse motion of arterial and venous PWs over the ventricle surfaces. We find that arterial PWs differ in CF phase from venous PWs over the surfaces of the ventricles consistent with arteriovenous PW phase coupling. We find a spatiotemporal difference in vascular PW phase between the ventral and dorsal ventricular surfaces, with the PWs arriving slightly sooner to the ventral surfaces. In humans undergoing neuroendoscopic surgery for hydrocephalus, we measure directly ventricle wall motions and the adjacent internal CSF pressure variations. We find that CSF pressure peaks slightly earlier in the ventral Third Ventricle than the dorsal Lateral Ventricle. When matched anatomically, the peri-ventricular vascular PW phase distribution in piglets complements the endo-ventricular CSF PW phase distribution in humans. This is consistent with a role for the ventricles in arteriovenous PW coupling and may add a framework for understanding hydrocephalus and other disturbances of intracranial pressure.

Citing Articles

The Development of Non-Invasive Optical Brain Pulse Monitoring: A Review.

Teo E, Petautschnig S, Chung S, Hellerstedt J, Savage J, Dixon B Med Devices (Auckl). 2024; 17:491-511.

PMID: 39678442 PMC: 11646379. DOI: 10.2147/MDER.S498589.


Deriving Automated Device Metadata From Intracranial Pressure Waveforms: A Transforming Research and Clinical Knowledge in Traumatic Brain Injury ICU Physiology Cohort Analysis.

Ack S, Dolmans R, Foreman B, Manley G, Rosenthal E, Zabihi M Crit Care Explor. 2024; 6(7):e1118.

PMID: 39016273 PMC: 11254120. DOI: 10.1097/CCE.0000000000001118.


Mechanical loading of the ventricular wall as a spatial indicator for periventricular white matter degeneration.

Visser V, Cacoilo A, Rusinek H, Weickenmeier J J Mech Behav Biomed Mater. 2023; 143:105921.

PMID: 37269602 PMC: 10266836. DOI: 10.1016/j.jmbbm.2023.105921.


Long-term recovery behavior of brain tissue in hydrocephalus patients after shunting.

Gholampour S, Frim D, Yamini B Commun Biol. 2022; 5(1):1198.

PMID: 36344582 PMC: 9640582. DOI: 10.1038/s42003-022-04128-8.


A neural stem cell paradigm of pediatric hydrocephalus.

Duy P, Rakic P, Alper S, Robert S, Kundishora A, Butler W Cereb Cortex. 2022; 33(8):4262-4279.

PMID: 36097331 PMC: 10110448. DOI: 10.1093/cercor/bhac341.


References
1.
Saikali S, Meurice P, Sauleau P, Eliat P, Bellaud P, Randuineau G . A three-dimensional digital segmented and deformable brain atlas of the domestic pig. J Neurosci Methods. 2010; 192(1):102-9. DOI: 10.1016/j.jneumeth.2010.07.041. View

2.
Park E, Dombrowski S, Luciano M, Zurakowski D, Madsen J . Alterations of pulsation absorber characteristics in experimental hydrocephalus. J Neurosurg Pediatr. 2010; 6(2):159-70. DOI: 10.3171/2010.5.PEDS09142. View

3.
Kulkarni A, Drake J, Mallucci C, Sgouros S, Roth J, Constantini S . Endoscopic third ventriculostomy in the treatment of childhood hydrocephalus. J Pediatr. 2009; 155(2):254-9.e1. DOI: 10.1016/j.jpeds.2009.02.048. View

4.
Meairs S, Alonso A . Ultrasound, microbubbles and the blood-brain barrier. Prog Biophys Mol Biol. 2006; 93(1-3):354-62. DOI: 10.1016/j.pbiomolbio.2006.07.019. View

5.
Zou R, Park E, Kelly E, Egnor M, Wagshul M, Madsen J . Intracranial pressure waves: characterization of a pulsation absorber with notch filter properties using systems analysis: laboratory investigation. J Neurosurg Pediatr. 2008; 2(1):83-94. DOI: 10.3171/PED/2008/2/7/083. View