Decreased prereceptorial glucocorticoid activating capacity in starvation due to an oxidative shift of pyridine nucleotides in the endoplasmic reticulum

FEBS Lett. 2010 Nov 19;584(22):4703-8. doi: 10.1016/j.febslet.2010.10.053. Epub 2010 Oct 28.

Abstract

Redox state of pyridine nucleotides of the endoplasmic reticulum (ER) lumen was determined in different nutritional conditions. NADPH-dependent cortisone reduction and NADP(+)-dependent cortisol oxidation were measured in rat liver microsomes, by utilizing the luminal 11β-hydroxysteroid dehydrogenase type 1 activity. Cortisone reduction decreased, while cortisol oxidation increased during onward starvation, showing that the luminal NADPH/NADP(+) ratio was substantially decreased. Cortisone or metyrapone addition caused a smaller decrease in NADPH fluorescence in microsomes from starved rats. The results demonstrate that nutrient supply is mirrored by the redox state of ER luminal pyridine nucleotides.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 11-beta-Hydroxysteroid Dehydrogenase Type 1 / metabolism
  • Animals
  • Cortisone / metabolism*
  • Endoplasmic Reticulum / metabolism*
  • Hydrocortisone / metabolism*
  • Liver / cytology
  • Liver / pathology
  • Male
  • Microsomes, Liver / metabolism
  • NADP / metabolism*
  • Oxidation-Reduction
  • Rats
  • Rats, Wistar
  • Starvation / metabolism*
  • Starvation / pathology*

Substances

  • NADP
  • 11-beta-Hydroxysteroid Dehydrogenase Type 1
  • Cortisone
  • Hydrocortisone