Long-term effects of hydrogen sulfide on the anabolic-catabolic balance of articular cartilage in vitro

• Published in: Nitric oxide Vol. 70; pp. 42 - 50
• Main Authors: Vela-Anero, Á., Hermida-Gómez, T., Gato-Calvo, L., Vaamonde-García, C., Díaz-Prado, S., Meijide-Faílde, R., Blanco, F.J., Burguera, E.F.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01-11-2017
• Subjects: Cartilage, Articular - drug effects; Cartilage, Articular - metabolism; Cartilage, Articular - pathology; Catabolism; Glycosaminoglycans - analysis; Glycosaminoglycans - metabolism; Human articular cartilage; Humans; Hydrogen sulfide; Hydrogen Sulfide - pharmacology; Immunohistochemistry; Interleukin-1beta - antagonists & inhibitors; Interleukin-1beta - pharmacology; Matrilin Proteins - analysis; Matrilin Proteins - metabolism; Matrix Metalloproteinase 13 - analysis; Matrix Metalloproteinase 13 - metabolism; Matrix Metalloproteinase 3 - analysis; Matrix Metalloproteinase 3 - metabolism; Morpholines - pharmacology; Organothiophosphorus Compounds - pharmacology; Osteoarthritis; Osteoarthritis - drug therapy; Osteoarthritis - metabolism; Osteoarthritis - pathology; Protective Agents - pharmacology; Proteoglycans; Sulfides - pharmacology; Time Factors; Hydrogen sulfide; Catabolism; Proteoglycans; Human articular cartilage; Osteoarthritis
• ISSN: 1089-8603; 1089-8611
• DOI: 10.1016/j.niox.2017.08.004

Healthy cartilage maintenance relies on an equilibrium among the anabolic and catabolic processes in chondrocytes. With the onset of osteoarthritis (OA), increased interleukin (IL)-1β levels induce an inhibition of the synthesis of extracellular matrix (ECM) proteins, as well as an increase in proteases. This eventually leads to a predominance of the catabolic phenotype and the progressive loss of articular cartilage. Hydrogen sulfide (H2S) is a small gaseous molecule recognized as the third endogenous gasotransmitter. When administered exogenously, it has shown anti-inflammatory and anti-catabolic properties in several in vitro and in vivo models. Here, OA cartilage disks were co-cultured in vitro with IL-1β (5 ng/ml) and NaSH or GYY4137 (200 or 1000 μM) for 21 days. The ability of these two H2S-producing compounds to avoid long term extracellular matrix (ECM) destruction was evaluated. We used a glycosaminoglycan (GAG) quantification kit histology and immunohistochemistry (IHC) to evaluate matrix proteins degradation and matrix metalloproteinases (MMP) abundance. Through the GAGs quantification assay, safranin O (S-O) and toluidine blue (TB) stains, and keratan/chondroitin sulfate (KS/ChS) IHCs it was shown that co-stimulation with H2S-forming reagents effectively avoided GAGs destruction. Both Masson's trichrome (MT) stain and collagen (col) type II IHC, as well as aggrecan (agg) IHC demonstrated that not only were these proteins protected but even promoted, their abundance being higher than in the basal condition. Further, stains also demonstrated that positivity in the inter-territorial and intra-cellular for the different matrix components were rescued, suggesting that NaSH and GYY4137 might also have pro-anabolic effects. In addition, a clear protective effect against the increased MMPs levels was seen, since increased MMP3 and 13 levels were subsequently reduced with the co-stimulation with sulfide compounds. In general, GYY4137 was more effective than NaSH, and increasing the dose improved the results.
This study demonstrates that H2S anti-catabolic effects, which had been previously proven in short-term (24–48 h) in vitro cellular models, are maintained over time directly in OA cartilage tissue.
•Co-stimulation with H2S improves the anabolic-catabolic balance in IL-1β-treated OA cartilage.•This is the result of a reduction in glucosaminoglycans and collagen type II loss induced by IL-1β.•H2S also partially inhibits matrix metalloproteinases 3 and 13 increase in this in vitro OA model.