Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
7
pubmed:dateCreated
2004-4-30
pubmed:abstractText
The beneficial actions of nonsteroidal anti-inflammatory drugs (NSAIDs) have been linked to their ability to inhibit inducible COX-2 at sites of inflammation, and their side effects (e.g., gastric damage) to inhibition of constitutive COX-1. Selective inhibitors of COX-2, such as celecoxib, etoricoxib, lumiracoxib, rofecoxib, and valdecoxib have been developed and the greatest recent growth in our knowledge in this area has been come from the clinical use of these compounds. Although clinical data indicate that COX-2 selectivity is associated with a reduction in severe gastrointestinal events, they also reveal there are roles for constitutive COX-2 within tissues such as the brain, kidney, pancreas, intestine, and blood vessels. We now better understand the roles of COX-1 and COX-2 in functions as disparate as the perception of pain and the progression of cancers. Clinical use of COX-2-selective compounds has ignited strong debates regarding potential side effects, most notably those within the cardiovascular system such as myocardial infarctions, strokes, and elevation in blood pressure. This review will discuss how the latest studies help us understand the roles of COX-1 and COX-2 and what clinically proven benefits the newer generation of COX-2-selective inhibitors offer
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
1530-6860
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
18
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
790-804
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:15117884-Alzheimer Disease, pubmed-meshheading:15117884-Animals, pubmed-meshheading:15117884-Anti-Inflammatory Agents, Non-Steroidal, pubmed-meshheading:15117884-Asthma, pubmed-meshheading:15117884-Cardiovascular Diseases, pubmed-meshheading:15117884-Colonic Neoplasms, pubmed-meshheading:15117884-Cyclooxygenase Inhibitors, pubmed-meshheading:15117884-Drug Design, pubmed-meshheading:15117884-Drug Eruptions, pubmed-meshheading:15117884-Female, pubmed-meshheading:15117884-Gastric Mucosa, pubmed-meshheading:15117884-Humans, pubmed-meshheading:15117884-Inflammation, pubmed-meshheading:15117884-Intestinal Mucosa, pubmed-meshheading:15117884-Kidney, pubmed-meshheading:15117884-Male, pubmed-meshheading:15117884-Mice, pubmed-meshheading:15117884-Pain Threshold, pubmed-meshheading:15117884-Peptic Ulcer, pubmed-meshheading:15117884-Pregnancy, pubmed-meshheading:15117884-Prostaglandin-Endoperoxide Synthases, pubmed-meshheading:15117884-Prostaglandins, pubmed-meshheading:15117884-Rats, pubmed-meshheading:15117884-Reproduction, pubmed-meshheading:15117884-Wound Healing
pubmed:year
2004
pubmed:articleTitle
Cyclooxygenases: new forms, new inhibitors, and lessons from the clinic.
pubmed:affiliation
The William Harvey Research Institute, Barts & the London, Queen Mary's School of Medicine and Dentistry, Charterhouse Square, London EC1M 6BQ, UK. t.d.warner@qmul.ac.uk
pubmed:publicationType
Journal Article, Review, Research Support, Non-U.S. Gov't