Differential effects of corticosterone on the colocalization of reelin and neuronal nitric oxide synthase in the adult hippocampus in wild type and heterozygous reeler mice

Brain Res. 2015 Jan 12:1594:274-83. doi: 10.1016/j.brainres.2014.10.050. Epub 2014 Oct 31.

Abstract

Repeated corticosterone (CORT) treatment induces a deficit in dentate gyrus subgranular zone reelin-positive cells, in maturation of newborn neurons, and results in a consistent depressive-like behavior. However, the molecular mechanisms underlying these processes are not known in detail. The purpose of the present study was to characterize the effect of three weeks of 20mg/kg CORT injections in the number of reelin and neuronal nitric oxide synthase (nNOS), as well as their colocalization, in hippocampal regions in wild type (WTM) and heterozygous reeler mice (HRM). ANOVA analysis shows a CORT×genotype interaction in the density of reelin+ cells co-localizing nNOS in the dentate subgranular zone and stratum-lacunosum moleculare, and in the density of nNOS+ cells in the hilus. There is a main effect of CORT in the density of both reelin+ and nNOS+ cells in the dentate subgranular zone and hilus, and in reelin+ cells in the molecular layer and CA3 stratum radiatum; and a main effect of genotype on the co-localization of both markers in the dentate subgranular zone, and in the density of reelin+ cell sin the stratum lacunosum moleculare. These alterations suggest a possible interconnection between reelin and nNOS expression that is altered by repeated CORT treatment.

Keywords: Hippocampus; Immunohistochemistry; Nitric oxide; Reelin deficits.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Adhesion Molecules, Neuronal / genetics
  • Cell Adhesion Molecules, Neuronal / metabolism*
  • Corticosterone / pharmacology*
  • Extracellular Matrix Proteins / genetics
  • Extracellular Matrix Proteins / metabolism*
  • Genotype
  • Hippocampus / drug effects*
  • Hippocampus / metabolism*
  • Immunohistochemistry
  • Male
  • Mice
  • Mice, Neurologic Mutants
  • Microscopy, Confocal
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism*
  • Nitric Oxide Synthase Type I / metabolism*
  • Reelin Protein
  • Serine Endopeptidases / genetics
  • Serine Endopeptidases / metabolism*

Substances

  • Cell Adhesion Molecules, Neuronal
  • Extracellular Matrix Proteins
  • Nerve Tissue Proteins
  • Reelin Protein
  • Nitric Oxide Synthase Type I
  • Reln protein, mouse
  • Serine Endopeptidases
  • Corticosterone