Long-term intermittent feeding restores impaired GR signaling in the hippocampus of aged rat

J Steroid Biochem Mol Biol. 2015 May:149:43-52. doi: 10.1016/j.jsbmb.2015.01.013. Epub 2015 Jan 20.

Abstract

Diminished glucocorticoid signaling is associated with an age-related decline in hippocampal functioning. In this study we demonstrate the effect of intermittent, every other day (EOD) feeding on the glucocorticoid hormone/glucocorticoid receptor (GR) system in the hippocampus of middle-aged (18-month-old) and aged (24-month-old) Wistar rats. In aged ad libitum-fed rats, a decrease in the level of total GR and GR phosphorylated at Ser(232) (pGR) was detected. Conversely, aged rats subjected to EOD feeding, starting from 6 months of age, showed an increase in GR and pGR levels and a higher content of hippocampal corticosterone. Furthermore, prominent nuclear staining of pGR was observed in CA1 pyramidal and DG granule neurons of aged EOD-fed rats. These changes were accompanied by increased Sgk-1 and decreased GFAP transcription, pointing to upregulated transcriptional activity of GR. EOD feeding also induced an increase in the expression of the mineralocorticoid receptor. Our results reveal that intermittent feeding restores impaired GR signaling in the hippocampus of aged animals by inducing rather than by stabilizing GR signaling during aging.

Keywords: Aging; Corticosterone; Dietary restriction; Glucocorticoid receptor isoforms; Hippocampus; Intermittent feeding.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • 11-beta-Hydroxysteroid Dehydrogenase Type 1 / analysis
  • 11-beta-Hydroxysteroid Dehydrogenase Type 1 / metabolism
  • Aging*
  • Animals
  • Corticosterone / analysis
  • Corticosterone / metabolism
  • Food Deprivation / physiology*
  • HSP90 Heat-Shock Proteins / analysis
  • HSP90 Heat-Shock Proteins / metabolism
  • Hippocampus / physiology*
  • Immediate-Early Proteins / genetics
  • Male
  • Phosphotransferases / analysis
  • Phosphotransferases / metabolism
  • Protein Serine-Threonine Kinases / genetics
  • RNA, Messenger / analysis
  • RNA, Messenger / genetics
  • Rats
  • Rats, Wistar
  • Receptors, Glucocorticoid / analysis
  • Receptors, Glucocorticoid / metabolism*
  • Signal Transduction*
  • Tacrolimus Binding Proteins / analysis
  • Tacrolimus Binding Proteins / metabolism
  • Up-Regulation

Substances

  • Cdk5r1 protein, rat
  • HSP90 Heat-Shock Proteins
  • Immediate-Early Proteins
  • RNA, Messenger
  • Receptors, Glucocorticoid
  • 11-beta-Hydroxysteroid Dehydrogenase Type 1
  • Phosphotransferases
  • Protein Serine-Threonine Kinases
  • serum-glucocorticoid regulated kinase
  • Tacrolimus Binding Proteins
  • Corticosterone