Effects of pretreatment with SKF-525A on triphenyltin metabolism and toxicity in mice

Toxicol Lett. 2000 Nov 20;117(3):145-50. doi: 10.1016/s0378-4274(00)00255-1.

Abstract

The effects of cytochrome P-450 inhibition by alpha-phenyl-alpha-propylbenzeneacetic acid 2-[diethylamino]-ethyl ester hydrochloride (SKF-525A), which inhibits the activity of a number of cytochrome P-450s, on triphenyltin metabolism and toxicity in mice were studied. At 24 h after triphenyltin administration, the triphenyltin levels in the tissues of SKF-525A-pretreated mice were about three times of those in the tissues of SKF-525A-untreated mice and the ratio of metabolites to parent triphenyltin in the tissues of SKF-525A-pretreated mice was lower than those in the tissues of SKF-525A-untreated mice. These data indicate that the pretreatment of SKF-525A decelerated the triphenyltin metabolism and increased triphenyltin accumulation in the tissues of mice. Although triphenyltin did not affect plasma glucose levels of in the SKF-525A-untreated mice, the triphenyltin produced marked hyperglycemia in SKF-525A-pretreated mice. These results suggest that the inhibition of cytochrome P-450 system enzymes by SKF-525A affects the metabolism and toxicity of triphenyltin and has a key role in inducing the hyperglycemic action of triphenyltin, i.e. by increasing triphenyltin accumulation in the mice.

MeSH terms

  • Alanine Transaminase / blood
  • Animals
  • Aspartate Aminotransferases / blood
  • Biotransformation
  • Blood Glucose / metabolism
  • Cytochrome P-450 Enzyme System / metabolism
  • Enzyme Inhibitors / pharmacology*
  • Male
  • Mice
  • Microsomes, Liver / drug effects
  • Microsomes, Liver / enzymology
  • Microsomes, Liver / metabolism
  • Organotin Compounds / pharmacokinetics*
  • Organotin Compounds / toxicity*
  • Proadifen / pharmacology*
  • Triglycerides / blood

Substances

  • Blood Glucose
  • Enzyme Inhibitors
  • Organotin Compounds
  • Triglycerides
  • Cytochrome P-450 Enzyme System
  • triphenyltin
  • Proadifen
  • Aspartate Aminotransferases
  • Alanine Transaminase