MadSci Network: General Biology |
Dear Heather, I apologize for taking so long to answer your question. Many pain relieving drugs, such as paracetamol (also called acetaminophen), act to inhibit the synthesis of a group of chemicals called prostaglandins. These drugs inhibit a group of enzyme termed cyclooxygenases. A recent report (Chandrasekharan et al. 2002) demonstrates that paracetamol inhibits an enzyme called cyclooxygenase 3 (COX-3). COX-3 is also inhibited by phenacetin, another analgesic. Other members of the cyclooxygenase family include COX-1 and COX-2, which are inhibited by aspirin and several nonsteroidal anti-inflammatory drugs (see the discussion at this web site: http://webcampus.med.drexel.edu/cme/medicine/nsaids/mechanisms.htm). COX-2 inhibitors have received much attention recently because they relieve pain and inflammation without causing the severe gastrointestinal distress (such as ulcers) that results from non-selective COX inhibitors. Thus, they are prescribed for treating chronic pain. Chandrasekharan et al (2002) COX-3, a cyclooxygenase-1 variant inhibited by acetaminophen and other analgesic/antipyretic drugs: cloning, structure, and expression. Proc Natl Acad Sci USA 99(21):13926-31.
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