A Minimally Invasive Rabbit Model of Progressive and Reproducible Disc Degeneration Confirmed by Radiology, Gene Expression, and Histology.
10.3340/jkns.2013.53.6.323
- Author:
Young Joon KWON
1
Author Information
1. Department of Neurosurgery, Sungkyunkwan University School of Medicine, Kangbuk Samsung Hospital, Seoul, Korea. neuriac@skku.edu
- Publication Type:Original Article
- Keywords:
Model, animal;
Intervertebral disc degeneration;
Minimally invasive procedure
- MeSH:
Aggrecans;
Biochemistry;
Gene Expression;
Hematoxylin;
Intervertebral Disc Degeneration;
Longitudinal Studies;
Magnetic Resonance Imaging;
Models, Animal;
Punctures;
Rabbits;
RNA, Messenger;
Spine
- From:Journal of Korean Neurosurgical Society
2013;53(6):323-330
- CountryRepublic of Korea
- Language:English
-
Abstract:
OBJECTIVE: To develop a simple, reproducible model of disc degeneration in rabbits through percutaneous annular puncture and to confirm the degree of degeneration over time. METHODS: Fifteen New Zealand white rabbits (4 to 5 months old and weighing approximately 3 to 3.5 kg each) underwent annular puncture of the L2-L3, L3-L4, and L4-L5 discs. Rabbits were sacrificed at 4, 8, or 20 weeks after puncture. For a longitudinal study to assess changes in disc height over time, serial X-rays were performed at 0, 2, 4, 8, and 20 weeks for rabbits in the 20-week group. Upon sacrifice, the whole spinal column and discs were extracted and analyzed with magnetic resonance imaging (MRI), real time reverse transcriptase-polymerase chain reaction, and histological staining. RESULTS: The X-rays showed a slow, progressive decrease in disc height over time. Significant disc space narrowing compared to preoperative disc height was observed during the time period (p<0.001). The MRI grade, aggrecan, and matrix metalloprotease-13 mRNA expression and hematoxylin and eosin/safranin O/anti-collagen II staining were consistently indicative of degeneration, supporting the results of the X-ray data. CONCLUSION: Percutaneous annular puncture resulted in slow, reproducible disc degeneration that was confirmed by radiology, biochemistry, and histology. This in vivo model can be used to study and evaluate the safety and efficacy of biologic treatments for degenerative disc disease.
