Abstract
There is increasing evidence that non-steroidal anti-inflammatory drugs (NSAIDs) can adversely affect bone repair. We have, therefore, studied the in vitro effects of NSAIDs, which differentially inhibit cyclooxygenases (COX), the prostaglandin/thromboxane synthesising enzymes, on human osteoblasts. Indomethacin and the new nitric oxide (NO)-donating NSAIDs block the activity of both COX-1 and COX-2. Indomethacin and 5,5-dimethyl-3-(3 fluorophenyl)-4-(4 methylsulphonal) phenyl-2 (5H)-furanone (DFU) reduced osteoblast numbers in a dose-dependant manner and increased collagen synthesis and alkaline phosphatase activity. The reduction in osteoblast numbers was not caused by loss of adhesion and was reversible. Neither NSAID influenced DNA synthesis. There was no difference between the effects of indomethacin and DFU. NO-NSAIDs did not affect cell numbers. These results suggest that care should be taken when administering NSAIDs to patients with existing skeletal problems and that NO-NSAlDs may be safer. © 2004 British Editorial Society of Bone and Joint Surgery.
Original language | English |
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Pages (from-to) | 444-449 |
Number of pages | 5 |
Journal | Journal of Bone and Joint Surgery - Series B |
Volume | 86 |
Issue number | 3 |
DOIs | |
Publication status | Published - Apr 2004 |
Keywords
- adverse effects: Acetaminophen
- metabolism: Alkaline Phosphatase
- adverse effects: Anti-Inflammatory Agents, Non-Steroidal
- adverse effects: Aspirin
- Cell Count
- Cells, Cultured
- biosynthesis: Collagen
- adverse effects: Cyclooxygenase Inhibitors
- biosynthesis: DNA
- adverse effects: Flurbiprofen
- adverse effects: Furans
- Humans
- adverse effects: Indomethacin
- adverse effects: Nitrates
- metabolism: Nitric Oxide
- therapeutic use: Nitric Oxide Donors
- drug effects: Osteoblasts
- metabolism: Prostaglandin-Endoperoxide Synthase
- Research Support, Non-U.S. Gov't