Abstract
Objectives:
The objectives of this study were to explore the change of intramedullary pressure over time in rats after different degrees of spinal cord contusion injury and to verify the hypothesis that the more serious the injury, the higher the intramedullary pressure.
Methods:
The control group rats underwent laminectomy only, whereas the rats in the three experimental groups were subjected to mild, moderate or severe 10th thoracic cord (T10) contusion injury after laminectomy. In addition, an intramedullary pressure of T10 was measured by a Millar Mikro-Tip pressure catheter (Millar Incorporated Company, Houston, TX, USA) immediately in the control group or at different time points after injury in the experimental groups.
Results:
The average intramedullary pressure of the rats in the control group was 6.88±1.67 mm Hg, whereas that of the rats in any injury group was significantly higher (P=0.000). There was statistical difference among the different time points in the mild or moderate injury group (P=0.007/0.017), but no in the severe (P=0.374). The curves of intramedullary pressure over time in the mild and moderate injury group were bimodal, peaking at 1 and 48 h after the injury. The intramedullary pressure after injury was positively correlated with the injury degree (r=0.438, P=0.000).
Conclusions:
The intramedullary pressure of the rats increased after traumatic spinal cord injury. If the injury was not serious, the intramedullary pressure fluctuated with time and peaked at 1 and 48 h after injury. If the injury was serious, the intramedullary pressure remained high. The more serious the injury, the higher the intramedullary pressure.
Similar content being viewed by others
Log in or create a free account to read this content
Gain free access to this article, as well as selected content from this journal and more on nature.com
or
References
Jägersberg M, Schaller C, Boström J, Schatlo B, Kotowski M, Thees C . Simultaneous bedside assessment of global cerebral blood flow and effective cerebral perfusion pressure in patients with intracranial hypertension. Neurocrit Care 2010; 12: 225–233.
Salinas NM . Ocular hypertension impairs optic nerve axonal transport leading to progressive retinal ganglion cell degeneration. Exp Eye Res 2010; 90: 168–183.
Ouyang H, Galle B, Li J, Nauman E, Shi R . Biomechanics of spinal cord injury: a multi- modal investigation using ex vivo guinea pig spinal cord white matter. J Neurotrauma 2008; 25: 19–29.
Young W . Spinal cord contusion models. Prog Brain Res 2002; 137: 231–255.
Saadoun S, Bell B, Verkman A, Papadopoulos M . Greatly improved neurological outcome after spinal cord compression injury in AQP4-deficient mice. Brain 2008; 131: 1087–1098.
Iida H, Tachibana S . Spinal cord intramedullary pressure: direct cord traction test. Neurol Med Chir 1995; 35: 75–77.
Waibl H . Zur Topographie der Medulla spinalis der Albinoratte (Rattus norvegicus. Adv Anat Embryol Cell Biol 1973; 47: 5–42.
Weirich SD, Cotler HB, Narayana PA, Hazle JD, Jackson EF, Coupe KJ et al. Histopathologic correlation of magnetic resonance imaging signal patterns in a spinal cord injury model. Spine 1990; 15: 630–638.
Wagner FC Jr, Dohrmann GJ, Bucy PC . Histopathology of transitory traumatic paraplegia in the monkey. J Neurosurg 1971; 35: 272–276.
Osterholm JL . Spinal pathways mediating traumatic hemorrhagic necrosis. Trans Am Neurol Assoc 1972; 97: 187.
Leonard AV, Thornton E, Vink R . The relative contribution of edema and hemorrhage to raised intrathecal pressure following traumatic spinal cord injury. J Neurotrauma 2015; 32: 397–402.
Dohrmann GJ, Wagner FC Jr, Bucy PC . The microvasculature in transitory traumatic paraplegia: an electron microscopic study in the monkey. J Neurosurg 1971; 35: 263–271.
Yashon D, Bingham WG Jr, Faddoul EM, Hunt WE . Edema of the spinal cord following experimental impact trauma. J Neurosurg 1973; 38: 693–697.
Torre JCDL. Spinal cord injury: review of basic and applied research. Spine 1981; 6: 315–335.
Hu A-M, Li J-J, Sun W, Yang D-G, Yang M-L, Du L-J et al. Myelotomy reduces spinal cord edema and inhibits aquaporin-4 and aquaporin-9 expression in rats with spinal cord injury. Spinal Cord 2015; 53: 98–102.
Chavanne A, Pettigrew DB, Holtz JR, Dollin N, Kuntz CI . Spinal cord intramedullary pressure in cervical kyphotic deformity: a cadaveric study. Spine 1976; 36: 1619–1626.
Ducker T, Kindt G, Kempe L . Pathological findings in acute experimental spinal cord trauma. J Neurosurg 1971; 35: 700–708.
Acknowledgements
This work was supported by the National Natural Science Foundation of China (81272164) and the Special Fund for Basic Scientific Research of Central Public Research Institutes (2014CZ-20).
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Competing interests
The authors declare no conflict of interest.
Rights and permissions
About this article
Cite this article
Dong, X., Yang, D., Li, J. et al. Intramedullary pressure changes in rats after spinal cord injury. Spinal Cord 54, 947–950 (2016). https://doi.org/10.1038/sc.2016.35
Received:
Revised:
Accepted:
Published:
Issue date:
DOI: https://doi.org/10.1038/sc.2016.35
This article is cited by
-
Therapeutic effects of rapamycin and surgical decompression in a rabbit spinal cord injury model
Cell Death & Disease (2020)


