TY - JOUR
T1 - Nucleotomy reduces the effects of cyclic compressive loading with unloaded recovery on human intervertebral discs
AU - Showalter, Brent L.
AU - Malhotra, Neil R.
AU - Vresilovic, Edward J.
AU - Elliott, Dawn M.
N1 - Funding Information:
We would like to thank Dhara B. Amin and Ian S. MacLean for performing some of the mechanical testing. Spines were acquired from National Disease Research Interchange, Philadelphia, PA and Platinum Training, Henderson, NV. This study was funded by NIH R01AR050052 , NSF Graduate Research Fellowship no. DGE-0822 , and a Neurosurgery Research and Education Foundation grant. None of the funding agencies played a direct role in study design, data collection, or data analysis.
PY - 2014/8/22
Y1 - 2014/8/22
N2 - The first objective of this study was to determine the effects of physiological cyclic loading followed by unloaded recovery on the mechanical response of human intervertebral discs. The second objective was to examine how nucleotomy alters the disc[U+05F3]s mechanical response to cyclic loading. To complete these objectives, 15 human L5-S1 discs were tested while intact and subsequent to nucleotomy. The testing consisted of 10,000 cycles of physiological compressive loads followed by unloaded hydrated recovery. Cyclic loading increased compression modulus (3%) and strain (33%), decreased neutral zone modulus (52%), and increased neutral zone strain (31%). Degeneration was not correlated with the effect of cyclic loading in intact discs, but was correlated with cyclic loading effects after nucleotomy, with more degenerate samples experiencing greater increases in both compressive and neutral zone strain following cyclic loading. Partial removal of the nucleus pulposus decreased the compression and neutral zone modulus while increasing strain. These changes correspond to hypermobility, which will alter overall spinal mechanics and may impact low back pain via altered motion throughout the spinal column. Nucleotomy also reduced the effects of cyclic loading on mechanical properties, likely due to altered fluid flow, which may impact cellular mechanotransduction and transport of disc nutrients and waste. Degeneration was not correlated with the acute changes of nucleotomy. Results of this study provide an ideal protocol and control data for evaluating the effectiveness of a mechanically-based disc degeneration treatment, such as a nucleus replacement.
AB - The first objective of this study was to determine the effects of physiological cyclic loading followed by unloaded recovery on the mechanical response of human intervertebral discs. The second objective was to examine how nucleotomy alters the disc[U+05F3]s mechanical response to cyclic loading. To complete these objectives, 15 human L5-S1 discs were tested while intact and subsequent to nucleotomy. The testing consisted of 10,000 cycles of physiological compressive loads followed by unloaded hydrated recovery. Cyclic loading increased compression modulus (3%) and strain (33%), decreased neutral zone modulus (52%), and increased neutral zone strain (31%). Degeneration was not correlated with the effect of cyclic loading in intact discs, but was correlated with cyclic loading effects after nucleotomy, with more degenerate samples experiencing greater increases in both compressive and neutral zone strain following cyclic loading. Partial removal of the nucleus pulposus decreased the compression and neutral zone modulus while increasing strain. These changes correspond to hypermobility, which will alter overall spinal mechanics and may impact low back pain via altered motion throughout the spinal column. Nucleotomy also reduced the effects of cyclic loading on mechanical properties, likely due to altered fluid flow, which may impact cellular mechanotransduction and transport of disc nutrients and waste. Degeneration was not correlated with the acute changes of nucleotomy. Results of this study provide an ideal protocol and control data for evaluating the effectiveness of a mechanically-based disc degeneration treatment, such as a nucleus replacement.
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U2 - 10.1016/j.jbiomech.2014.05.018
DO - 10.1016/j.jbiomech.2014.05.018
M3 - Article
C2 - 24957922
AN - SCOPUS:84905270543
SN - 0021-9290
VL - 47
SP - 2633
EP - 2640
JO - Journal of Biomechanics
JF - Journal of Biomechanics
IS - 11
ER -