Open AccessEffects of Epomediol on Ethinyloestradiol‐Induced Changes in Glutathione Homeostasis in the Rat
Author(s) -
Cuevas Maria Jose,
Almar Mar,
GonzálezGallego Javier
Publication year - 2002
Publication title -
pharmacology & toxicology
Language(s) - English
Resource type - Journals
eISSN - 1600-0773
pISSN - 0901-9928
DOI - 10.1034/j.1600-0773.2002.900302.x
Subject(s) - glutathione , cholestasis , endocrinology , medicine , homeostasis , kidney , chemistry , pharmacology , biology , biochemistry , enzyme
Epomediol is a synthetic terpenoid compound that has been reported to reduce ethinyloestradiol‐induced cholestasis. The choleretic action of epomediol is related to an increase in both the bile acid‐dependent and independent fractions of bile flow, but the role of glutathione metabolism and transport is still unknown. This study was aimed to evaluate if changes in glutathione homeostasis could contribute to the beneficial effects of epomediol in rats with ethinyloestradiol‐induced cholestasis. When compared to control animals, ethinyloestradiol treatment resulted in a significant decrease in the liver concentration of reduced (GSH) and oxidized glutathione. Both GSH and oxidized glutathione concentrations returned to normal in animals receiving ethinyloestradiol plus epomediol. Ethinyloestradiol administration induced a significant decrease in plasma and renal GSH and the tripeptide was almost absent from bile. Combined treatment with epomediol plus ethinyloestradiol normalised renal GSH and both biliary and liver cysteine were significantly increased. Liver and kidney γ‐glutamyltranspeptidase activities were higher in rats receiving ethinyloestradiol and still remained elevated in animals with the combined treatment. Liver γ‐glutamylcysteine synthetase activity rose significantly by administration of ethinyloestradiol plus epomediol but the corresponding mRNA levels were not modified. Changes in glutathione homeostasis and higher biliary levels of GSH amino acid constituents could contribute to the beneficial effects of epomediol in rats with ethinyloestradiol‐induced cholestasis.