Inflammatory profiles in canine intervertebral disc degeneration

Publication date

2016-01-13

Authors

Willems, NicoleISNI 0000000492962986
Tellegen, AnnaISNI 0000000492496604
Bergknut, NiklasISNI 0000000113254577
Creemers, Laura B
Wolfswinkel, Jeannette
Freudigmann, Christian
Benz, Karin
Grinwis, Guy C MISNI 0000000394959548
Tryfonidou, Marianna AORCID 0000-0002-2333-7162ISNI 0000000388930095
Meij, Björn PORCID 0000-0002-0165-1169ISNI 0000000388662836

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Abstract

BACKGROUND: Intervertebral disc (IVD) disease is a common spinal disorder in dogs and degeneration and inflammation are significant components of the pathological cascade. Only limited studies have studied the cytokine and chemokine profiles in IVD degeneration in dogs, and mainly focused on gene expression. A better understanding is needed in order to develop biological therapies that address both pain and degeneration in IVD disease. Therefore, in this study, we determined the levels of prostaglandin E2 (PGE2), cytokines, chemokines, and matrix components in IVDs from chondrodystrophic (CD) and non-chondrodystrophic (NCD) dogs with and without clinical signs of IVD disease, and correlated these to degeneration grade (according to Pfirrmann), or herniation type (according to Hansen). In addition, we investigated cyclooxygenase 2 (COX-2) expression and signs of inflammation in histological IVD samples of CD and NCD dogs. RESULTS: PGE2 levels were significantly higher in the nucleus pulposus (NP) of degenerated IVDs compared with non-degenerated IVDs, and in herniated IVDs from NCD dogs compared with non-herniated IVDs of NCD dogs. COX-2 expression in the NP and annulus fibrosus (AF), and proliferation of fibroblasts and numbers of macrophages in the AF significantly increased with increased degeneration grade. GAG content did not significantly change with degeneration grade or herniation type. Cytokines interleukin (IL)-2, IL-6, IL-7, IL-8, IL-10, IL-15, IL-18, immune protein (IP)-10, tumor necrosis factor (TNF)-α, and granulocyte macrophage colony-stimulating factor (GM-CSF) were not detectable in the samples. Chemokine (C-C) motif ligand (CCL)2 levels in the NP from extruded samples were significantly higher compared with the AF of these samples and the NP from protrusion samples. CONCLUSIONS: PGE2 levels and CCL2 levels in degenerated and herniated IVDs were significantly higher compared with non-degenerated and non-herniated IVDs. COX-2 expression in the NP and AF and reactive changes in the AF increased with advancing degeneration stages. Although macrophages invaded the AF as degeneration progressed, the production of inflammatory mediators seemed most pronounced in degenerated NP tissue. Future studies are needed to investigate if inhibition of PGE2 levels in degenerated IVDs provides effective analgesia and exerts a protective role in the process of IVD degeneration and the development of IVD disease.

Keywords

Low back pain, Dog, PGE2, Prostaglandin, Herniation, Chondrodystrophic, Non-chondrodystrophic

Citation

Willems, N, Tellegen, A R, Bergknut, N, Creemers, L B, Wolfswinkel, J, Freudigmann, C, Benz, K, Grinwis, G C M, Tryfonidou, M A & Meij, B P 2016, 'Inflammatory profiles in canine intervertebral disc degeneration', BMC Veterinary Research, vol. 12, no. 10. https://doi.org/10.1186/s12917-016-0635-6