Abstract | OBJECTIVE: MATERIALS AND METHODS: RESULTS: In the SCID mouse co-implantation model, the MMP-13 inhibitor reduced cartilage destruction by 75%. In the CIA model of RA, the MMP-13 inhibitor resulted in a significant and dose-dependent decrease in clinical symptoms as well as of cartilage erosion by 38% (30 mg/kg), 28% (10 mg/kg) and 21% (3 mg/kg). No significant effects were seen in the AIA model. No toxic effects were seen in all three animal models. CONCLUSION: Although several MMPs in concert with other proteinases have a role in the process of cartilage destruction, there is a need for highly selective MMP inhibitors to reduce severe side effects that occur with non-specific inhibitors. Significant inhibition of MMP-13 reduced cartilage erosions in two of three tested animal models of RA. These results strongly support the development of this class of drugs to reduce or halt joint destruction in patients with RA.
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Authors | Astrid Jüngel, Caroline Ospelt, Mark Lesch, Melissa Thiel, Teresa Sunyer, Olivier Schorr, Beat A Michel, Renate E Gay, Christoph Kolling, Craig Flory, Steffen Gay, Michel Neidhart |
Journal | Annals of the rheumatic diseases
(Ann Rheum Dis)
Vol. 69
Issue 5
Pg. 898-902
(May 2010)
ISSN: 1468-2060 [Electronic] England |
PMID | 19497915
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antirheumatic Agents
- Enzyme Inhibitors
- Matrix Metalloproteinase Inhibitors
- Matrix Metalloproteinase 13
- Matrix Metalloproteinase 1
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Topics |
- Administration, Oral
- Animals
- Antirheumatic Agents
(administration & dosage, therapeutic use)
- Arthritis, Experimental
(drug therapy, enzymology, pathology)
- Arthritis, Rheumatoid
(drug therapy, enzymology, pathology)
- Cartilage, Articular
(pathology)
- Disease Models, Animal
- Dose-Response Relationship, Drug
- Drug Evaluation, Preclinical
(methods)
- Enzyme Inhibitors
(administration & dosage, therapeutic use)
- Female
- Humans
- Male
- Matrix Metalloproteinase 1
(metabolism)
- Matrix Metalloproteinase 13
(metabolism)
- Matrix Metalloproteinase Inhibitors
- Mice
- Mice, SCID
- Rabbits
- Synovial Membrane
(enzymology)
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