Effects of a water-soluble prodrug of vitamin E on doxorubicin-induced toxicity in mice

Yoshiko Nagata, Jiro Takata, A. Yoshiharu Karube, Yoshikazu Matsushima

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11 Citations (Scopus)


Effects of the administration of a water-soluble prodrug of vitamin E on doxorubicine (DXR)-induced lethal and oxidative toxicity in mice were studied. The prodrug used was d-α-tocopheryl N,N-dimethylaminoacetate hydrochloride (TDMA). It was intravenously administered to animals 2 h prior to an intraperitoneal administration of DXR (15 mg/kg). The single preadministration of the prodrug (10 - 50 mg/kg equivalent for d-α- tocopherol) delayed the DXR-induced death and the ameliorative effect was TDMA-dose dependent. The extent of total lipid peroxidation of the heart and liver was assessed by 2-thiobarbituric acid reactant substance levels. DXR significantly accelerated lipid peroxidation in the liver but not in the heart. The elevation of liver lipid peroxide was significantly suppressed to a normal range by a single preadministration of TDMA (50 mg/kg equivalent for d-α-tocopherol). TDMA did not significantly affect the antitumor activity of DXR in mice inoculated with L1210 leukemia cells.

Original languageEnglish
Pages (from-to)698-702
Number of pages5
JournalBiological and Pharmaceutical Bulletin
Issue number7
Publication statusPublished - 1999 Jul


  • D-α-tocopheryl N,N-dimethylaminoacetate
  • Doxorubicin
  • Lipid peroxidation
  • Oxidative stress
  • Vitamin E
  • Water soluble prodrug

ASJC Scopus subject areas

  • Pharmacology
  • Pharmaceutical Science


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