Abstract
Since Felix Hoffman first synthesized acetylsalicylic acid (aspirin) in 1897, prostaglandin synthesis inhibitors have been widely used as effective anti-inflammatory, analgesic and anti-pyretic agents. Much of our present understanding regarding prostaglandins (PGs) in fact derives from observing the effects of aspirin and non-steroidal anti-inflammatory drugs (NSAIDs) which inhibit PG synthesis by interfering with one of the rate-limiting enzymes, cyclooxygenase. In addition to regulating immune responses, pain, and fever, PGs are now implicated as playing an important role as autocrine/paracrine modulators of cellular responses such as mitogenesis and apoptosis.
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Park, J.M., Schnermann, J.B., Briggs, J.P. (1999). Cyclooxygenase-2. In: Baskin, L.S., Hayward, S.W. (eds) Advances in Bladder Research. Advances in Experimental Medicine and Biology, vol 462. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-4737-2_13
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DOI: https://doi.org/10.1007/978-1-4615-4737-2_13
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