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Comparative Pathophysiology and Toxicology of Cyclooxygenases (Hardcover)
Loot Price: R3,607
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Comparative Pathophysiology and Toxicology of Cyclooxygenases (Hardcover)
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The first thorough review of cyclooxygenase inhibitors, including
their toxicity mechanisms and toxicopathological risks
Cyclooxygenases (COXs) are enzymes responsible for the formation of
an important class of biological mediators called prostanoids.
Prostanoids such as prostaglandins mediate inflammatory and
anaphylactic reactions. For those suffering from inflammation and
pain, the pharmacological inhibition of COXs, with non-steroidal
anti-inflammatory drugs (NSAIDs), such as ibuprofen, can provide
relief. Yet the use of NSAIDs can trigger toxicological effects as
well, leading to potential health risks. Comparative
Pathophysiology and Toxicology of Cyclooxygenases provides a
comprehensive overview of how COX inhibitors affect various bodily
systems, specifically the toxicity mechanisms triggered when the
COX enzyme is inhibited. The book provides an introduction to the
discovery of cyclooxygenases, their use as therapeutic agents, as
well as an historical perspective. Shedding light on the
differences in expression, pathophysiology, and toxicology of COX
inhibitors across species, the book offers a systematic examination
of the effects and pathophysiology of COX inhibitors and their
mechanisms of toxicity, beginning with the GI tract. Subsequent
chapters cover: * The pathophysiology of COX inhibition on bone,
tendon, and ligament healing * COX inhibitors and renal system
pathophysiology and mechanisms of toxicity * The pathophysiologic
role of COX inhibition in the ocular system * COX inhibition and
the respiratory and cardiovascular systems The book also sheds
light on the latest research devoted to developing COX inhibitors
with no adverse side-effects. The first book to offer a thorough
comparative look at the toxicological effects of COX inhibitors
throughout the body, this invaluable resource will help advance the
research and development of safer and more effective COX drugs.
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