The cardioprotector monoHER does not interfere with the pharmacokinetics or the metabolism of the cardiotoxic agent doxorubicin in mice

Cancer Chemother Pharmacol. 2003 Apr;51(4):306-10. doi: 10.1007/s00280-003-0582-3. Epub 2003 Mar 22.

Abstract

Purpose: Monohydroxyethylrutoside (monoHER) has proved to be a good protector against doxorubicin-induced cardiotoxicity without interfering with the antitumor effect of doxorubicin. The aim of the present study was to determine whether there is a pharmacokinetic interaction between monoHER and doxorubicin which may be involved in monoHER cardioprotection.

Methods: Mice were treated with monoHER (500 mg x kg(-1) i.v.) alone, monoHER 5 min after doxorubicin (10 mg x kg(-1) i.v.), doxorubicin alone and doxorubicin 5 min after monoHER. The levels of monoHER and doxorubicin(ol) in plasma and heart tissue were measured by HPLC 24 h and 48 h after monoHER and doxorubicin administration, respectively.

Results: The areas under the concentration-time curves (AUCs) of monoHER and doxorubicin(ol) were not affected by the coadministered drug. No changes were observed in pharmacokinetic parameters such as initial and final half-lives, mean residence time, clearance and volume of distribution of monoHER and doxorubicin(ol) after single or combined administration.

Conclusion: The cardioprotection of monoHER in mice is not caused by a pharmacokinetic interaction between monoHER and doxorubicin.

MeSH terms

  • Animals
  • Area Under Curve
  • Cardiotonic Agents / pharmacokinetics*
  • Doxorubicin* / analogs & derivatives*
  • Doxorubicin* / metabolism
  • Doxorubicin* / pharmacokinetics
  • Doxorubicin* / toxicity
  • Drug Interactions
  • Drug Therapy, Combination
  • Half-Life
  • Hydroxyethylrutoside / pharmacokinetics*
  • Injections, Intravenous
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Myocardium / metabolism*
  • Tissue Distribution

Substances

  • Cardiotonic Agents
  • Hydroxyethylrutoside
  • Doxorubicin
  • adriamycinol