An in vivo study on the rabbit lumbar spine model.
Effects of temporary dynamic distraction on intervertebral discs were studied on the lumbar spine rabbit model to characterize the changes associated with disc distraction and to evaluate feasibility of temporary disc distraction to previously compressed discs in order to stimulate disc regeneration.
Studies have shown that accelerated degeneration of the intervertebral disc results from altered mechanical loading conditions. The development of methods for the prevention of disc degeneration and the restoration of disc tissue that has already degenerated are needed.
New Zealand white rabbits (n = 32) were used for this study. The rabbits were randomly assigned to one of five groups. In 12 animals, the discs were first loaded for 28 days using a custom-made external loading device to stimulate disc degeneration. After 28 days loading time, the discs in six animals were distracted for 7 days and in six animals for 28 days using the same external device, however, modified as dynamic distraction device. In six animals, the discs were distracted for 28 days without previous loading; and in six animals, the discs were loaded for 28 days and afterwards the loading device removed for 28 days for recovery without distraction. Six animals were sham operated. The external device was situated; however, the discs remained undistracted and they also served as controls. After 28 to 56 days loading and distraction time, the animals were killed and the lumbar spine was harvested for examination. Disc height, disc morphology, cell viability, relative neutral zone, and tangent modulus were measured.
After 28 days of loading, the discs demonstrated a significant decrease in disc space. Histologically, disorganization of the architecture of the anulus occurred. The number of dead cells increased significantly in the anulus and cartilage endplate. These changes were re-versible after 28 days of distraction. The disc thickness increased significantly as compared with the specimens from the 28 days loading group without distraction. Histologically, the discs showed signs of tissue regeneration after 28 days of distraction. The number of dead cells decreased significantly in comparison with the loaded discs without distraction. The flexibility of compressed discs was higher than of compressed/distracted discs.
The results of this study suggest that disc regeneration can be induced by axial dynamic distraction in the rabbit intervertebral disc. The decompressed rabbit intervertebral discs showed signs of tissue recovery on a biologic, cellular, and a biomechanical level after 28 days of distraction.
Studies have shown that accelerated degeneration of the intervertebral disc results from altered mechanical loading conditions. A total of 32 New Zealand white rabbits were used to study the effects of temporary dynamic distraction on intervertebral discs in the lumbar spine to characterize the changes associated with disc distraction to evaluate feasibility of temporary disc distraction to previously compressed discs in order to stimulate disc regeneration.
From the *Department of Orthopaedic Surgery, University of California, San Francisco, CA; †Department of Orthopaedic Surgery, University of Heidelberrg, Heidelberg, Germany; and ‡Department of Pathology, Krankenhaus München-Bogenhausen, Munich, Germany.
Acknowledgment date: August 11, 2003. First revision date: October 20, 2003. Acceptance date: February 5, 2004.
The manuscript submitted does not contain information about medical device(s)/drug(s).
Supported in parts by Centerpulse Orthopedics Ltd, a Zimmer Company.
Corporate/Industry and Institutional funds were received in support of this work. No benefits in any form have been or will be received from a commercial party related directly or indirectly to the subject of this manuscript.
Address correspondence and reprint requests to Markus W. Kroeber, MD, PhD, Department of Orthopaedic Surgery University of California, San Francisco 500 Parnassus Ave., MU 320 West San Francisco, CA 94143-0728. E-mail: Markus_Kroeber@yahoo.de