Adriamycin-induced changes of creatine kinase activity in vivo and in cardiomyocyte culture

Toxicology. 1999 May 3;134(1):51-62. doi: 10.1016/s0300-483x(99)00039-6.

Abstract

Adriamycin (ADM) is an anthracycline anti-neoplastic agent, whose clinical effectiveness is limited by severe side effects, including cardiotoxicity. The toxic effects of ADM are likely to be the consequence of the generation of free radicals. This study demonstrates that ADM induces significant changes in the activity of the oxidative sensitive enzyme creatine kinase (CK) in the heart in vivo and in a cardiomyocyte culture model. The changes observed are likely to reflect the ability of ADM to damage the plasma membrane of cardiac cells and to induce the direct inactivation of CK. The role for ADM-derived free radicals is one of the possible mechanisms for the CK inactivation observed during the ADM treatment.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Antibiotics, Antineoplastic / toxicity*
  • Cells, Cultured
  • Creatine Kinase / drug effects*
  • Creatine Kinase / immunology
  • Creatine Kinase / metabolism
  • Doxorubicin / toxicity*
  • Heart / drug effects*
  • Male
  • Myocardium / enzymology
  • Rats
  • Rats, Sprague-Dawley
  • Superoxide Dismutase / drug effects
  • Superoxide Dismutase / immunology
  • Superoxide Dismutase / metabolism

Substances

  • Antibiotics, Antineoplastic
  • Doxorubicin
  • Superoxide Dismutase
  • Creatine Kinase