Abstract
Cyclooxygenase (COX) inhibitors are widely used analgesic and anti-inflammatory drugs. Owing to undesirable effects caused by unselective COX inhibitors and selective COX-2 inhibitors, microsomal prostaglandin E(2) synthase-1 has been considered as an alternative target for the development of analgesic drugs. However, recent findings question the usefulness of this terminal synthase as a promising drug target for pain therapy.
Publication types
-
Research Support, Non-U.S. Gov't
-
Review
MeSH terms
-
Animals
-
Cyclooxygenase Inhibitors / pharmacology
-
Cyclooxygenase Inhibitors / therapeutic use*
-
Humans
-
Intramolecular Oxidoreductases / antagonists & inhibitors*
-
Intramolecular Oxidoreductases / metabolism
-
Models, Biological
-
Pain / drug therapy*
-
Pain / enzymology
-
Prostaglandin-E Synthases
Substances
-
Cyclooxygenase Inhibitors
-
Intramolecular Oxidoreductases
-
PTGES protein, human
-
Prostaglandin-E Synthases