Low toxicity of diphenyl diselenide in rabbits: a long-term study

Basic Clin Pharmacol Toxicol. 2007 Jul;101(1):47-55. doi: 10.1111/j.1742-7843.2007.00073.x.

Abstract

Selenium compounds, like diphenyl diselenide (Ph(2)Se(2)), possess glutathione peroxidase (GSHPx)-like activities and other antioxidant properties. The aim of this study was to evaluate the effects of a long-term oral supplementation with Ph(2)Se(2) on various toxicological parameters in rabbits. Adult New Zealand male rabbits were divided into four groups: Group I served as control; Groups II, III and IV received 0.3, 3.0 and 30 p.p.m. of Ph(2)Se(2) pulverized in the chow for 8 months. A number of toxicological parameters were examined in liver, kidney, cerebral cortex and hippocampus, such as delta-aminolaevulinic acid dehydratase (delta-ALA-D), catalase (CAT), GSHPx activities, non-protein thiol (-SH), lipid peroxidation and ascorbic acid levels. The results indicated that supplementation 30 p.p.m. Ph(2)Se(2 )significantly increased delta-ALA-D activity in liver and in cerebral cortex. Non-protein -SH levels were significantly increased in liver but not in kidney, cerebral cortex and hippocampus of rabbits. Ascorbic acid content was significantly lower in the liver and cerebral cortex after supplementation with 30 p.p.m. Ph(2)Se(2). Conversely, no alterations in GSHPx and CAT activities, nor in thiobarbituric acid reactive substances levels were observed in rabbit tissues. These results indicate that oral supplementation with Ph(2)Se(2) is relatively secure in rabbits after 8 months of exposure. The findings encourage further experiments on the potential therapeutic effects of such compound.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antioxidants / adverse effects*
  • Antioxidants / pharmacokinetics
  • Ascorbic Acid / metabolism
  • Benzene Derivatives / adverse effects*
  • Benzene Derivatives / pharmacokinetics
  • Brain / metabolism*
  • Catalase / metabolism
  • Dose-Response Relationship, Drug
  • Glutathione Peroxidase / metabolism
  • Kidney / metabolism*
  • Lipid Peroxidation / physiology
  • Liver / metabolism*
  • Male
  • Organoselenium Compounds / adverse effects*
  • Organoselenium Compounds / pharmacokinetics
  • Porphobilinogen Synthase / metabolism
  • Rabbits
  • Thiobarbituric Acid Reactive Substances / metabolism
  • Time Factors

Substances

  • Antioxidants
  • Benzene Derivatives
  • Organoselenium Compounds
  • Thiobarbituric Acid Reactive Substances
  • diphenyldiselenide
  • Catalase
  • Glutathione Peroxidase
  • Porphobilinogen Synthase
  • Ascorbic Acid