Estrogen modulates neural-immune interactions through intracellular signaling pathways and antioxidant enzyme activity in the spleen of middle-aged ovariectomized female rats

J Neuroimmunol. 2014 Feb 15;267(1-2):7-15. doi: 10.1016/j.jneuroim.2013.11.003. Epub 2013 Nov 12.

Abstract

Modulation of neural-immune interactions by estrogen in the spleens of ovariectomized (OVX) middle-aged female rats was examined. Con A-induced lymphoproliferation, splenic tyrosine hydroxylase (TH) and nerve growth factor (NGF) expression, levels of p-ERK 1/2, p-CREB, and p-Akt, and activity of superoxide dismutase decreased in OVX rats while estrogen treatment enhanced their expression, levels, and activity. Also, estrogen treatment enhanced Con A-induced IFN-γ production and decreased Con A-induced IL-2 production compared to OVX animals. In contrast, estrogen increased the extent of lipid peroxidation and protein carbonyl formation while OVX induced a decline in protein carbonyl formation. These results suggest that estrogen enhances neural-immune interactions while simultaneously affecting it through generation of free radicals as reflected by increased lipid peroxidation and protein carbonyl formation.

Keywords: Akt; CREB; Cytokine; ERK; Nerve growth factor; Tyrosine hydroxylase.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Age Factors
  • Animals
  • Antioxidants / metabolism*
  • Cell Proliferation / drug effects
  • Concanavalin A / pharmacology
  • Cytokines / metabolism
  • Dose-Response Relationship, Drug
  • Drug Interactions
  • Estrogens / pharmacology*
  • Female
  • Lipid Peroxidation / drug effects
  • Lymphocytes / drug effects*
  • Nerve Growth Factors / metabolism
  • Nitric Oxide / metabolism
  • Ovariectomy
  • Protein Carbonylation / drug effects
  • Rats
  • Rats, Sprague-Dawley
  • Signal Transduction / drug effects*
  • Spleen / cytology
  • Spleen / drug effects*
  • Superoxide Dismutase / metabolism
  • Tyrosine 3-Monooxygenase / metabolism

Substances

  • Antioxidants
  • Cytokines
  • Estrogens
  • Nerve Growth Factors
  • Concanavalin A
  • Nitric Oxide
  • Tyrosine 3-Monooxygenase
  • Superoxide Dismutase