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Selective COX-2 Inhibitors - Pharmacology, Clinical Effects and Therapeutic Potential (Paperback, Softcover reprint of the original 1st ed. 1998)
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Discovery Miles 27 530
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Selective COX-2 Inhibitors - Pharmacology, Clinical Effects and Therapeutic Potential (Paperback, Softcover reprint of the original 1st ed. 1998)
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Total price: R2,763
Discovery Miles: 27 630
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The mainstay of therapy for rheumatoid disease is the non-steroid
antiinflammatory drugs (NSAIDs), despite their inherent
gastrointestinal toxicity and ability to cause renal damage in
susceptible patients. The theory that the beneficial and toxic
effects of NSAIDs stem from a reduction in prostanoid production
through inhibition of cyclooxygenase implied that particular
toxicities were inevitable with NSAIDs and would always be
correlated with efficacy. However, over the years, it became
apparent that at therapeutic doses, some NSAIDs had greater toxic
side-effects than others, a fact not explained by the general
theory. A significant clarification arose from the discovery that
there are two distinct isoforms of COX, a constitutive enzyme
(COX-I) responsible for the production of prostanoids necessary for
platelet aggregation and protection of the gastric mucosa and
kidney; and an inducible enzyme (COX-2) that is newly synthesized
at sites of tissue damage and produces prostaglandins that manifest
pathological effects. It became clear that different NSAIDs had
greater or lesser effects on COX-I when used in therapeutic doses,
explaining the variation in side-effects. ' The elucidation of the
crystal structure of these different enzymes and the skills of
medicinal chemists have led to the synthesis of new chemicals with
a selectivity for the inducible enzyme, and thus with therapeutic
efficacy without those toxic effects result ing from inhibition of
the constitutive enzyme.
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