Unopposed Estrogen Supplementation/Progesterone Deficiency in Post-Reproductive Age Affects the Secretory Profile of Resident Macrophages in a Tissue-Specific Manner in the Rat

Am J Reprod Immunol. 2015 Nov;74(5):445-56. doi: 10.1111/aji.12424. Epub 2015 Aug 26.

Abstract

Problem: The influence of unopposed estrogen replacement/isolated progesterone deficiency on macrophage production of pro-inflammatory/anti-inflammatory mediators in the post-reproductive age was studied.

Method of study: Considering that in the rats post-ovariectomy the circulating estradiol, but not progesterone level rises to the values in sham-operated controls, 20-month-old rats ovariectomized at the age of 10 months served as an experimental model. Estrogen and progesterone receptor expression, secretion of pro- and anti-inflammatory cytokines, and arginine metabolism end-products were examined in splenic and peritoneal macrophages under basal conditions and following lipopolysaccharide (LPS) stimulation in vitro.

Results: Almost all peritoneal and a subset of splenic macrophages expressed the intracellular progesterone receptor. Ovariectomy diminished cytokine production by splenic (IL-1β) and peritoneal (TNF-α, IL-1β, IL-10) macrophages and increased the production of IL-10 by splenic and TGF-β by peritoneal cells under basal conditions. Following LPS stimulation, splenic macrophages from ovariectomized rats produced less TNF-α and more IL-10, whereas peritoneal macrophages produced less IL-1β and TGF-β than the corresponding cells from sham-operated rats. Ovariectomy diminished urea production in both subpopulations of LPS-stimulated macrophages.

Conclusion: Although long-lasting isolated progesterone deficiency in the post-reproductive age differentially affects cytokine production in the macrophages from distinct tissue compartments, in both subpopulations, it impairs the pro-inflammatory/anti-inflammatory cytokine secretory balance.

Keywords: Aged AO rats; cytokine production; iNOS/arginase activity; ovariectomy; peritoneal macrophages; splenic macrophages.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arginase / metabolism
  • Cytokines / metabolism*
  • Estradiol / blood
  • Female
  • Macrophages / metabolism*
  • Nitric Oxide Synthase Type II / metabolism
  • Ovariectomy
  • Progesterone / blood
  • Rats
  • Receptors, Estrogen / metabolism
  • Receptors, Progesterone / metabolism

Substances

  • Cytokines
  • Receptors, Estrogen
  • Receptors, Progesterone
  • Progesterone
  • Estradiol
  • Nitric Oxide Synthase Type II
  • Arginase