Studies of methyl 2-nitroimidazole-1-acetohydroxamate (KIN-804) 2: effect on certain antioxidant enzyme systems in mice bearing Ehrlich ascites carcinoma

Biol Pharm Bull. 2000 Feb;23(2):195-8. doi: 10.1248/bpb.23.195.

Abstract

In order to decrease toxicity and/or increase radiosensitizing activity, a new 2-nitroimidazole derivative, methyl 2-nitroimidazole-1-acetohydroxamate (KIN-804), was synthesized to solve the problem of tumor hypoxia. Evaluation of the efficiency of KIN-804 was carried out through studying the antioxidant enzyme system: The superoxide dismutase (SOD), catalase and lipid peroxide levels provide a rough index of the balance between free radical generation and scavenging. Female albino mice were inoculated with Ehrlich ascites carcinoma (EAC) in the thigh. The administration of KIN-804 (i.p. 80 mg/kg body weight) was carried out 20 min before localized irradiation of 10 Gy. In general, the data revealed that KIN-804 administration, followed or not by gamma irradiation, exerted significant inhibition of SOD and catalase activities accompanied by a significant increase in lipid peroxide level in tumor-bearing mice.

MeSH terms

  • Animals
  • Antioxidants / metabolism*
  • Carcinoma, Ehrlich Tumor / enzymology*
  • Catalase / blood
  • Catalase / metabolism
  • Catalase / radiation effects
  • Female
  • Hydroxamic Acids / pharmacology*
  • Hypoxia / enzymology
  • Lipid Peroxides / blood
  • Lipid Peroxides / metabolism
  • Lipid Peroxides / radiation effects
  • Liver / enzymology
  • Lung / enzymology
  • Mice
  • Nitroimidazoles / pharmacology*
  • Radiation-Sensitizing Agents / pharmacology*
  • Superoxide Dismutase / blood
  • Superoxide Dismutase / metabolism
  • Superoxide Dismutase / radiation effects

Substances

  • Antioxidants
  • Hydroxamic Acids
  • Lipid Peroxides
  • Nitroimidazoles
  • Radiation-Sensitizing Agents
  • 2-nitroimidazole-1-methylacetohydroxamate
  • Catalase
  • Superoxide Dismutase