Abstract
Among other non-antibiotic properties, tetracyclines inhibit matrix metalloproteinases and are currently under study for the treatment of osteoarthritis. Quaternary ammonium conjugates of tetracyclines were synthesized by direct alkylation of the amine function at the 4-position with methyl iodide. When tested in vitro, they inhibited cytokine-induced MMP expression to a lesser extent than parent tetracyclines. This was compensated by an improved inhibition of MMP catalytic activity. Since inhibition of collagen degradation was maintained these derivatives could be potent drug candidates for cartilage-targeted chondroprotective treatment.
Publication types
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Evaluation Study
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Cartilage, Articular / drug effects
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Cartilage, Articular / enzymology
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Chondrosarcoma / drug therapy
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Chondrosarcoma / enzymology
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Chondrosarcoma / pathology
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Collagen / drug effects
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Collagen / metabolism
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Humans
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In Vitro Techniques
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Matrix Metalloproteinase Inhibitors*
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Matrix Metalloproteinases / metabolism
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Protease Inhibitors / chemical synthesis
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Protease Inhibitors / chemistry
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Protease Inhibitors / pharmacology*
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Proteoglycans / drug effects
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Proteoglycans / metabolism
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Rabbits
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Tetracyclines / chemical synthesis*
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Tetracyclines / chemistry
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Tetracyclines / pharmacology
Substances
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Matrix Metalloproteinase Inhibitors
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Protease Inhibitors
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Proteoglycans
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Tetracyclines
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Collagen
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Matrix Metalloproteinases