In:
Global Spine Journal, SAGE Publications, Vol. 2, No. 1_suppl ( 2012-06), p. s-0032-1319890-s-0032-1319890
Abstract:
During the degeneration process, tissue resorption causes a progressive and important decrease in intervertebral disk height. The main characteristics of disk degeneration are intradiscal clefts and teardrops. It is accepted that matrix-degrading enzymes, such as matrix metalloproteinases (MMPs), play an important role in disk tissue degeneration and destruction. Materials and Methods This study involved 42 patients between 26 and 69 years of age who underwent surgery for lumbar disk herniation (46 disk spaces). Tissue sections were used to immunolocalize MMP-3. The number of labeled cells was determined using morphometric analysis. Cell proliferation, cleft and teardrop formation, granular matrix changes, and mucosal degeneration were statistically assessed. Additionally, enzymatic gelatinolytic activity was determined using zymography. MMP-3 levels and histological degeneration scores were compared using the Pfirrmann classification, a radiologic disk degeneration grading system. Results The intradiscal expression of MMPs in the nucleus pulposus and annulus fibrosus cells was confirmed using immunohistochemistry, and gelatinolytic enzymatic activity was confirmed with in situ zymography. A significant relationship was determined between disk degeneration, characterized by intradiscal cleft and teardrop formation, and MMP-3 levels. Disk cell proliferation and matrix degeneration (granular changes and mucosal degeneration) were also found to be related to MMP-3 expression. Similarly, a relationship between enzymatic activity and cleft formation was determined. Conclusion Our findings support the hypothesis that MMP-3 enzyme levels play an important role in IVD degeneration. This association is supported by the high correlation between cleft and teardrop formation and MMP expression. These findings indicate the important role of MMPs in the loss of normal disk function as a result of IVD degeneration, which causes lumbar pain. I confirm having declared any potential conflict of interest for all authors listed on this abstract Yes Disclosure of Interest None declared Kanemoto M, Hukuda S, Komiya Y, Katsuura A, Nishioka J. Immunohistochemical study of matrix metalloproteinase-3 and tissue inhibitor of metalloproteinase-1 human intervertebral discs. Spine 1996;21(1):1–8 Kang JD, Stefanovic-Racic M, McIntyre LA, Georgescu HI, Evans CH. Toward a biochemical understanding of human intervertebral disc degeneration and herniation. Contributions of nitric oxide, interleukins, prostaglandin E2, and matrix metalloproteinases. Spine 1997;22(10):1065–073 Crean JK, Roberts S, Jaffray DC, Eisenstein SM, Duance VC. Matrix metalloproteinases in the human intervertebral disc: role in disc degeneration and scoliosis. Spine 1997;22(24):2877–2884
Type of Medium:
Online Resource
ISSN:
2192-5682
,
2192-5690
DOI:
10.1055/s-0032-1319890
Language:
English
Publisher:
SAGE Publications
Publication Date:
2012
detail.hit.zdb_id:
2648287-3
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