Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/137308
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Type: Journal article
Title: Characterising spinal cerebrospinal fluid flow in the pig with phase-contrast magnetic resonance imaging
Author: Bessen, M.A.
Gayen, C.D.
Quarrington, R.D.
Walls, A.C.
Leonard, A.V.
Kurtcuoglu, V.
Jones, C.F.
Citation: Fluids and Barriers of the CNS, 2023; 20(1):1-13
Publisher: Springer Nature
Issue Date: 2023
ISSN: 2045-8118
2045-8118
Statement of
Responsibility: 
Madeleine Amy Bessen, Christine Diana Gayen, Ryan David Quarrington, Angela Catherine Walls, Anna Victoria Leonard, Vartan Kurtcuoglu, and Claire Frances Jones
Abstract: Background: Detecting changes in pulsatile cerebrospinal fuid (CSF) fow may assist clinical management decisions, but spinal CSF fow is relatively understudied. Traumatic spinal cord injuries (SCI) often cause spinal cord swelling and subarachnoid space (SAS) obstruction, potentially causing pulsatile CSF fow changes. Pigs are emerging as a favoured large animal SCI model; therefore, the aim of this study was to characterise CSF fow along the healthy pig spine. Methods: Phase-contrast magnetic resonance images (PC-MRI), retrospectively cardiac gated, were acquired for fourteen laterally recumbent, anaesthetised and ventilated, female domestic pigs (22–29 kg). Axial images were obtained at C2/C3, T8/T9, T11/T12 and L1/L2. Dorsal and ventral SAS regions of interest (ROI) were manually segmented. CSF fow and velocity were determined throughout a cardiac cycle. Linear mixed-efects models, with post-hoc comparisons, were used to identify diferences in peak systolic/diastolic fow, and maximum velocity (cranial/caudal), across spinal levels and dorsal/ventral SAS. Velocity wave speed from C2/C3 to L1/L2 was calculated. Results: PC-MRI data were obtained for 11/14 animals. Pulsatile CSF fow was observed at all spinal levels. Peak systolic fow was greater at C2/C3 (dorsal: − 0.32±0.14 mL/s, ventral: − 0.15±0.13 mL/s) than T8/T9 dorsally (− 0.04±0.03 mL/s; p<0.001), but not diferent ventrally (− 0.08±0.08 mL/s; p=0.275), and no diference between thoracolumbar levels (p>0.05). Peak diastolic fow was greater at C2/C3 (0.29±0.08 mL/s) compared to T8/T9 (0.03±0.03 mL/s, p<0.001) dorsally, but not diferent ventrally (p=1.000). Cranial and caudal maximum velocity at C2/C3 were greater than thoracolumbar levels dorsally (p<0.001), and T8/T9 and L1/L2 ventrally (p=0.022). Diastolic velocity wave speed was 1.41±0.39 m/s dorsally and 1.22±0.21 m/s ventrally, and systolic velocity wave speed was 1.02±0.25 m/s dorsally and 0.91±0.22 m/s ventrally. Conclusions: In anaesthetised and ventilated domestic pigs, spinal CSF has lower pulsatile fow and slower velocity wave propagation, compared to humans. This study provides baseline CSF fow at spinal levels relevant for future SCI research in this animal model.
Keywords: Cerebrospinal fluid; Pulsatile; Spine; Flow; Velocity; Phase-contrast magnetic resonance imaging; Pig
Rights: © The Author(s) 2023. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativeco mmons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
DOI: 10.1186/s12987-022-00401-4
Grant ID: http://purl.org/au-research/grants/arc/DP190101209
http://purl.org/au-research/grants/nhmrc/1072387
Published version: http://dx.doi.org/10.1186/s12987-022-00401-4
Appears in Collections:Medicine publications

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