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Copper and aspirin treatment increase the antioxidant activity of plasma.

Abstract
Copper (Cu) complexes of a number of compounds have increased anti-inflammatory efficacy over the native compound. In the present study, Cu and acetylsalicylic acid (ASA) were administered to rabbits over a one week period. At the end of this time, ocular inflammation was induced by intravitreal injection of endotoxin. ASA caused a slight reduction in the inflammatory response at 24 hours, but this response was not further decreased when Cu was added to the treatment regimen. However, there was a gradual and significant increase in antioxidant activity in the plasma of animals in the combined treatment group which could not be accounted for by a Cu-ASA complex, an increase in the concentration of known plasma protein antioxidants (ceruloplasmin and transferrin) or an increase in superoxide dismutase activity. The compound(s) responsible for this increased activity has a molecular weight greater than 10,000 Da. A large increase in plasma antioxidant activity may have a protective effect in other models of inflammation and provide a mechanism for the proven increase in anti-inflammatory efficacy of Cu-chelates of many compounds.
AuthorsM C McGahan
JournalAgents and actions (Agents Actions) Vol. 31 Issue 1-2 Pg. 59-64 (Aug 1990) ISSN: 0065-4299 [Print] Switzerland
PMID2285023 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Anti-Inflammatory Agents, Non-Steroidal
  • Endotoxins
  • Transferrin
  • Copper
  • Superoxide Dismutase
  • Ceruloplasmin
  • Aspirin
Topics
  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal
  • Aqueous Humor (enzymology, metabolism)
  • Aspirin (pharmacology)
  • Ceruloplasmin (metabolism)
  • Copper (pharmacology)
  • Endotoxins (toxicity)
  • Eye Diseases (blood, chemically induced)
  • Inflammation (blood, chemically induced)
  • Lipid Peroxidation (drug effects)
  • Molecular Weight
  • Oxidation-Reduction
  • Rabbits
  • Superoxide Dismutase (metabolism)
  • Transferrin (metabolism)

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