Activation of P-450-Dependent Monooxygenases Modulates the Diuretic Effect of Histochrome in Rats

Bull Exp Biol Med. 2015 Oct;159(6):750-2. doi: 10.1007/s10517-015-3066-7. Epub 2015 Oct 29.

Abstract

We studied the role of the liver monooxygenase system in pharmacological activity of histochrome, a pharmaceutical form of echinochrome A. In experiments on rats, benzonal, an inductor of the monooxygenase system of phenobarbytal type, significantly potentiated the diuretic effect of histochrome. Benzonal withdrawal was followed by a natriuretic reaction. In view of the known inverse relation between the biological effect of the drug and the rate of its metabolism, our findings suggest that the effects of echinochrome A on some kidney excretory function parameters are produced not by native agent, but one of its metabolites.

Keywords: benzonal; histochrome; microsomal oxidation.

MeSH terms

  • Animals
  • Barbiturates / pharmacology*
  • Cytochrome P-450 Enzyme System / physiology
  • Diuresis / drug effects
  • Diuretics / pharmacology*
  • Drug Interactions
  • Enzyme Activation / drug effects
  • Enzyme Activation / physiology
  • Female
  • Liver / drug effects
  • Liver / physiology
  • Male
  • Mixed Function Oxygenases / metabolism
  • Mixed Function Oxygenases / physiology*
  • Naphthoquinones / pharmacology*
  • Rats
  • Rats, Wistar

Substances

  • Barbiturates
  • Diuretics
  • Naphthoquinones
  • histochrome
  • Cytochrome P-450 Enzyme System
  • Mixed Function Oxygenases
  • benzobarbital