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Improved Non-Steroid Anti-Inflammatory Drugs: COX-2 Enzyme Inhibitors (Paperback, Softcover reprint of the original 1st ed. 1996)
Loot Price: R2,779
Discovery Miles 27 790
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Improved Non-Steroid Anti-Inflammatory Drugs: COX-2 Enzyme Inhibitors (Paperback, Softcover reprint of the original 1st ed. 1996)
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Total price: R2,789
Discovery Miles: 27 890
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In 1971, Vane proposed that the mechanism of action of the
aspirin-like drugs was through their inhibition of prostaglandin
biosynthesis. Since then, there has been intense interest in the
interaction between this diverse group of inhibitors and the enzyme
known as cyclooxygenase (COX). It exists in two isoforms, COX-l and
COX-2 (discovered some 5 years ago). Over the last two decades
several new drugs have reached the market based on COX-l enzyme
screens. Elucidation of the three-dimensional structure of COX-l
has provided a new understanding for the actions of COX inhibitors.
The constitutive isoform of COX, COX-l has clear physiological
functions. Its activation leads, for instance, to the production of
prostacyclin which when released by the endothelium is
anti-thrombogenic and anti-atherosclerotic, and in the gastric
mucosa is cyto protective. COX-l also generates prostaglandins in
the kidney, where they help to maintain blood flow and promote
natriuresis. The inducible isoform, COX-2, was discovered through
its activity being increased in a number of cells by pro
inflammatory stimuli. A year or so later, COX-2 was identified as a
distinct isoform encoded by a different gene from COX-I. COX-2 is
induced by inflammatory stimuli and by cytokines in migratory and
other cells. Thus the anti-inflammatory actions of non-steroid
anti-inflammatory drugs (NSAIDs) may be due to the inhibition of
COX-2, whereas the unwanted side-effects such as irritation of the
stomach lining and toxic effects on the kidney are due to
inhibition of the constitutive enzyme, COX-I.
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