New selective COX-2 inhibitors
Conventional nonsteroidal anti-inflammatory drugs (NSAIDs) inhibit both of the cyclooxygenase (COX-1 and COX-2) enzymes to varying degrees; consequently, they impair prostaglandin production in all tissues, causing adverse effects, especially in the gastrointestinal tract, respiratory system (aspiri...
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Veröffentlicht in: | Pain reviews 2000-04, Vol.7 (1), p.3 |
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Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | Conventional nonsteroidal anti-inflammatory drugs (NSAIDs) inhibit both of the cyclooxygenase (COX-1 and COX-2) enzymes to varying degrees; consequently, they impair prostaglandin production in all tissues, causing adverse effects, especially in the gastrointestinal tract, respiratory system (aspirin-induced asthma), kidney and haematological system. Unfortunately, side-effects are common when contraindications to their use. The anti-inflammatory actions of the NSAIDs are mediated by COX-2 inhibition, while the adverse effects are considered to be predominantly caused by COX-1 inhibition. Therefore, the selective inhibition of COX-2 inhibitors offers real hope for safer NSAIDs; specific agents have now been developed to do this. Selective COX-2 inhibitors are effective anti-inflammatory agents, but their analgesic efficacy is still unclear. While they have significantly less gastrointestinal and antiplatelet effects, the acute renal and pulmonary effects of selective COX-2 inhibitors have not been fully clarified. Moreover, there are issues concerning their long-term safety because the inhibition of constitutive COX-2, which appears to have some important physiological functions, may still cause adverse effects. |
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ISSN: | 0968-1302 1477-0318 |