4.5 Article

TIME COURSE QUANTIFICATION OF SPASTIC HYPERTONIA FOLLOWING SPINAL HEMISECTION IN RATS

Journal

NEUROSCIENCE
Volume 167, Issue 1, Pages 185-198

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.neuroscience.2010.01.064

Keywords

muscle tone; spasticity; stretch reflex; hemisection; spinal cord injury

Categories

Funding

  1. National Science Council
  2. National Health Research Institutes of Taiwan [NSC 95-2221-E-006-010-MY3, NHRI-EX95-9524E1, NHRI-EX98-9535EI]

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Progressive changes in the muscle tone and stretch reflex after spinal cord injury (SCI) provide insight into the time-course development of spasticity. This study quantified the time-course changes of hypertonia for rats following SCI of T8 hemisection. A miniature manual stretching device measured the reactive torque via a pair of pressure sensing balloons; the angular displacement was measured via an optoelectronic device. Various stretching frequencies were tested, specifically 1/3, 1/2, 1, 3/2 and 2 Hz. The reactive torque and angular displacement were used to derive the viscous and elastic components representing the viscosity and stiffness of the rat's ankle joint. The enhanced velocity-dependent properties of spasticity were observed in the SCI hemisection rats (n=9) but not in the controls (n=9). Time-course measurements from pre-surgery to 56 days following SCI showed that the muscle tone of the hemisection rats dropped immediately after spinal shock and then gradually increased to reach a peak around 21 days postinjury (P<0.01). The muscle tone remained at least 75% of the peak value up to the end of an 8 week observation period (P<0.05). The changes of muscle tone can also be verified from the electrophysiological evaluations of electromyography (EMG) (P<0.05). In addition to conventional BBB motor behavior score, our results provided time-course quantification of the biomechanical and electrophysiological properties of muscle tone from the onset of SCI. Such data are useful for investigating progressive recovery of spinal damage in animal model and for future objective assessment of improved treatment for SCI human subjects. Crown Copyright (C) 2010 Published by Elsevier Ltd on behalf of IBRO. All rights reserved.

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