Superoxide dismutase triggers activation of "primed" platelets

Arch Biochem Biophys. 1991 Aug 15;289(1):180-3. doi: 10.1016/0003-9861(91)90458-u.

Abstract

Superoxide dismutase (SOD) triggers activation of human platelets exposed to subthreshold concentrations of arachidonic acid and collagen. The subthreshold concentrations used are not able to activate platelets but "prime" platelets to be activated by SOD. The addition of SOD to arachidonic acid-or collagen-primed platelets induced aggregation, thromboxane A2 production, and release of [3H]serotonin. Superoxide dismutase does not have any effect on resting platelets and ADP-, thrombin-, calcium ionophore A23187-, PAF-, or U46619-stimulated platelets. Furthermore, superoxide dismutase-dependent platelet activation is fully prevented by catalase and/or aspirin, suggesting a role for H2O2 and the involvement of the cyclooxygenase pathway of arachidonic acid in such activation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Arachidonic Acid
  • Arachidonic Acids / pharmacology
  • Aspirin / pharmacology
  • Blood Platelets / drug effects
  • Blood Platelets / metabolism
  • Catalase / pharmacology
  • Collagen / pharmacology
  • Humans
  • Male
  • Platelet Activation / drug effects*
  • Platelet Aggregation / drug effects
  • Serotonin / blood
  • Superoxide Dismutase / pharmacology*
  • Thromboxane A2 / blood

Substances

  • Arachidonic Acids
  • Arachidonic Acid
  • Serotonin
  • Thromboxane A2
  • Collagen
  • Catalase
  • Superoxide Dismutase
  • Aspirin