Establishment of a goat model of lumbar static and dynamic instability for the research on intervertebral disc degeneration

Chen Zhijie, Zhou Zhi, Tian Ziyang, Wang Zhenwei, Li Zhanchun

PDF(5578 KB)
PDF(5578 KB)
Journal of Chongqing Medical University ›› 2024, Vol. 49 ›› Issue (04) : 376-383. DOI: 10.13406/j.cnki.cyxb.003468
Basic research

Establishment of a goat model of lumbar static and dynamic instability for the research on intervertebral disc degeneration

Author information +
History +

Abstract

Objective To establish a practical large animal model of intervertebral disc degeneration(IVDD) for the simulation of the influence of local factors in the human body and the role of pathophysiological stress load on IVDD. Methods In this study,lumbar dynamic and static instability(LDSI) surgery was performed to damage the posterior column structure of the goat spine; the muscles including erector spinae,latissimus dorsi,longissimus lumborum,and spinalis were ligated to destroy the dynamic stability of the lumbar spine,and the spinous process,supraspinous ligament,and interspinous ligament were ligated to destroy the static stability of the lumbar spine,resulting in the imbalance of dynamic and static forces of the lumbar spine and the loss of the stability of the posterior column. With biomechanical stability as the breakthrough point,a goat model of lumbar dynamic and static instability was established without destroying the structural integrity of the intervertebral disc,and during 52 weeks of postoperative follow-up,lumbar spine X-ray,magnetic resonance imaging(MRI),and histopathological changes were used to evaluate disc height index(DHI),Pfirrmann MRI grade,and Masuda histological score. Results In the LDSI group,the DHI of goat lumbar spine was 0.184±0.015 at week 0 before surgery,0.105±0.006 at 26 weeks after surgery,and 0.075±0.007 at 52 weeks after surgery (0 week vs. 26 weeks:P<0.05;26 weeks vs. 52 weeks:P<0.05). In the LDSI group,the Pfirrmann grade of goat lumbar spine was 1.167±0.408 at week 0 before surgery,2.333±0.516 at 26 weeks after surgery,and 3.667±0.817 at 52 weeks after surgery(0 week vs. 26 weeks:P<0.05;26 weeks vs. 52 weeks:P<0.05). In the LDSI group,the Masuda histological score of goat lumbar spine was 3.500±0.577 at week 0 before surgery,6.250±0.957 at 26 weeks after surgery,and 8.000±0.816 at 52 weeks after surgery(0 week vs. 26 weeks:P<0.05;26 weeks vs. 52 weeks:P<0.05). Conclusion LDSI can cause the reduction in the height of the intervertebral disc,the blurring of endplate boundary,and the reduction in water content in goats. It simulates the process of IVDD caused by long-term repeated strain of human body without destroying the structural integrity of the intervertebral disc,which is more in line with the real condition of human body and may provide help for research on the pathogenesis of IVDD.

Key words

intervertebral disc degeneration / goat model / lumbar static and dynamic instability

Cite this article

Download Citations
Chen Zhijie , Zhou Zhi , Tian Ziyang , et al . Establishment of a goat model of lumbar static and dynamic instability for the research on intervertebral disc degeneration. Journal of Chongqing Medical University. 2024, 49(04): 376-383 https://doi.org/10.13406/j.cnki.cyxb.003468

References

1
GBD Disease and Injury Incidence and Prevalence Collaborators. Global,regional,and national incidence,prevalence,and years lived with disability for 354 diseases and injuries for 195 countries and territories,1990-2017:a systematic analysis for the Global Burden of Disease Study 2017[J]. Lancet2018392(10159):1789-1858.
2
Wu AM March L Zheng XQ,et al. Global low back pain prevalence and years lived with disability from 1990 to 2017:estimates from the Global Burden of Disease Study 2017[J]. Ann Transl Med20208(6):299.
3
Vlaeyen JWS Maher CG Wiech K,et al. Low back pain[J]. Nat Rev Dis Primers20184:52.
4
Maher C Underwood M Buchbinder R. Non-specific low back pain[J]. Lancet2017389(10070):736-747.
5
Xin JG Wang YJ Zheng Z,et al. Treatment of intervertebral disc degeneration[J]. Orthop Surg202214(7):1271-1280.
6
Wang YD Kang JH Guo XD,et al. Intervertebral disc degeneration models for pathophysiology and regenerative therapy-benefits and limitations[J]. J Invest Surg202235(4):935-952.
7
Jin L Balian G Li XJ. Animal models for disc degeneration-an update[J]. Histol Histopathol201833(6):543-554.
8
Hoogendoorn RJ Wuisman PI Smit TH,et al. Experimental intervertebral disc degeneration induced by chondroitinase ABC in the goat[J]. Spine200732(17):1816-1825.
9
Fazzalari NL Costi JJ Hearn TC,et al. Mechanical and pathologic consequences of induced concentric anular tears in an ovine model[J]. Spine200126(23):2575-2581.
10
Hoogendoorn RJ Helder MN Kroeze RJ,et al. Reproducible long-term disc degeneration in a large animal model[J]. Spine200833(9):949-954.
11
Beckstein JC Sen S Schaer TP,et al. Comparison of animal discs used in disc research to human lumbar disc:axial compression mechanics and glycosaminoglycan content[J]. Spine200833(6):E166-E173.
12
Krijnen MR Mensch D van Dieen JH,et al. Primary spinal segment stability with a stand-alone cage:in vitro evaluation of a successful goat model[J]. Acta Orthop200677(3):454-461.
13
Elliott DM Yerramalli CS Beckstein JC,et al. The effect of relative needle diameter in puncture and sham injection animal models of degeneration[J]. Spine200833(6):588-596.
14
Martin JT Gorth DJ Beattie EE,et al. Needle puncture injury causes acute and long-term mechanical deficiency in a mouse model of intervertebral disc degeneration[J]. J Orthop Res201331(8):1276-1282.
15
Masuda K Aota Y Muehleman C,et al. A novel rabbit model of mild,reproducible disc degeneration by an anulus needle puncture:correlation between the degree of disc injury and radiological and histological appearances of disc degeneration[J]. Spine200530(1):5-14.
16
Sasaki M Takahashi T Miyahara K,et al. Effects of chondroitinase ABC on intradiscal pressure in sheep:an in vivo study[J]. Spine200126(5):463-468.
17
Chan SCW Bürki A Bonél HM,et al. Papain-induced in vitro disc degeneration model for the study of injectable nucleus pulposus therapy[J]. Spine J201313(3):273-283.
18
Masuda K Imai Y Okuma M,et al. Osteogenic protein-1 injection into a degenerated disc induces the restoration of disc height and structural changes in the rabbit anular puncture model[J]. Spine200631(7):742-754.
19
Han B Zhu K Li FC,et al. A simple disc degeneration model induced by percutaneous needle puncture in the rat tail[J]. Spine200833(18):1925-1934.
20
Zhang Y He F Chen Z,et al. Melatonin modulates IL-1β-induced extracellular matrix remodeling in human nucleus pulposus cells and attenuates rat intervertebral disc degeneration and inflammation[J]. Aging201911(22):10499-10512.
21
Pfirrmann CW Metzdorf A Zanetti M,et al. Magnetic resonance classification of lumbar intervertebral disc degeneration[J]. Spine200126(17):1873-1878.
22
Nishimura K Mochida J. Percutaneous reinsertion of the nucleus pulposus. An experimental study[J]. Spine199823(14):1531-1538;discussion1539.
23
Zeng Y Chen C Liu W,et al. Injectable microcryogels reinforced alginate encapsulation of mesenchymal stromal cells for leak-proof delivery and alleviation of canine disc degeneration[J]. Biomaterials201559:53-65.
24
Daly C Ghosh P Jenkin G,et al. A review of animal models of intervertebral disc degeneration:pathophysiology,regeneration,and translation to the clinic[J]. Biomed Res Int20162016:5952165.
25
Rousseau MA A Ulrich JA Bass EC,et al. Stab incision for inducing intervertebral disc degeneration in the rat[J]. Spine200732(1):17-24.
26
Kim KS Yoon ST Li J,et al .Disc degeneration in the rabbit:a biochemical and radiological comparison between four disc injury models[J]. Spine200530(1):33-37.
27
Nuckley DJ Kramer PA del Rosario A,et al. Intervertebral disc degeneration in a naturally occurring primate model:radiographic and biomechanical evidence[J]. J Orthop Res200826(9):1283-1288.
28
Wei FX Zhong R Zhou ZY,et al. In vivo experimental intervertebral disc degeneration induced by bleomycin in the rhesus monkey[J]. BMC Musculoskelet Disord201415:340.
29
Gruber HE Johnson T Norton HJ,et al. The sand rat model for disc degeneration:radiologic characterization of age-related changes:cross-sectional and prospective analyses[J]. Spine200227(3):230-234.
30
Platenberg RC Hubbard GB Ehler WJ,et al. Spontaneous disc degeneration in the baboon model:magnetic resonance imaging and histopathologic correlation[J]. J Med Primatol200130(5):268-272.
31
Zhang YJ Drapeau S Howard SA,et al. Transplantation of goat bone marrow stromal cells to the degenerating intervertebral disc in a goat disc injury model[J]. Spine201136(5):372-377.
32
Zhang YJ Drapeau S An HS,et al. Histological features of the degenerating intervertebral disc in a goat disc-injury model[J]. Spine201136(19):1519-1527.
33
DS Shono Y Oda I,et al. Effects of chondroitinase ABC and chymopapain on spinal motion segment biomechanics. An in vivo biomechanical,radiologic,and histologic canine study[J]. Spine199722(16):1828-1834;discussion 1834-1835.
34
Lai A Chow DH Siu SW,et al. Effects of static compression with different loading magnitudes and durations on the intervertebral disc:an in vivo rat-tail study[J]. Spine200833(25):2721-2727.
35
Millecamps M Tajerian M Naso L,et al. Lumbar intervertebral disc degeneration associated with axial and radiating low back pain in ageing SPARC-null mice[J]. Pain2012153(6):1167-1179.

Comments

PDF(5578 KB)

Accesses

Citation

Detail

Sections
Recommended

/