The role of 17β-estradiol in the regulation of antioxidant enzymes via the Nrf2-Keap1 pathway in the livers of CBA/H mice

Life Sci. 2015 Jun 1:130:57-65. doi: 10.1016/j.lfs.2015.03.014. Epub 2015 Mar 26.

Abstract

Aims: We aimed to explore the impact of surgical 17β-estradiol (E2) deprivation/administration on the expression of antioxidant enzymes with an emphasis on the alteration of the NF-E2-related factor 2/Kelch-like ECH-associated protein 1 (Nrf2/Keap1) pathway under physiological conditions in the livers of CBA/H mice of both sexes.

Main methods: Hepatic oxidative stress markers were determined by measuring lipid peroxidation and DNA damage using the comet assay. The expression and activities of two isoforms of superoxide dismutase (Sod-1, Sod-2) and catalase (Cat) were studied using real-time PCR, Western blot and spectrophotometrical analyses. The effect of E2 on Nrf2/Keap1 protein levels and localization was assessed using cytosolic and nuclear fractions.

Key findings: We demonstrate the E2-mediated repression of the antioxidant enzymes Sod-1, Sod-2 and Cat in the livers of ovariectomized mice treated with E2 and its association with a decreased level of Nrf2/Keap1 proteins in the nucleus. We observed beneficial effects of long-term E2 administration on lipid peroxidation but not on DNA damage in the livers of ovariectomized mice.

Significance: The results of this study may additionally confirm the protective ability of E2 in prolonging the onset of age-related disease in females that ultimately contributes to their longer lifespan.

Keywords: 17β-estradiol; Cat; Keap1; Nrf2; ROS; Sex-related; Sod-1; Sod-2.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing / metabolism*
  • Animals
  • Antioxidants / metabolism*
  • Cytoskeletal Proteins / metabolism*
  • DNA Damage / drug effects
  • Estradiol / administration & dosage
  • Estradiol / metabolism
  • Estradiol / pharmacology*
  • Female
  • Kelch-Like ECH-Associated Protein 1
  • Lipid Peroxidation / drug effects
  • Liver / metabolism*
  • Male
  • Mice
  • Mice, Inbred CBA
  • NF-E2-Related Factor 2 / metabolism*
  • Oxidative Stress / drug effects
  • Oxidative Stress / physiology
  • Real-Time Polymerase Chain Reaction
  • Superoxide Dismutase / metabolism

Substances

  • Adaptor Proteins, Signal Transducing
  • Antioxidants
  • Cytoskeletal Proteins
  • Keap1 protein, mouse
  • Kelch-Like ECH-Associated Protein 1
  • NF-E2-Related Factor 2
  • Estradiol
  • Superoxide Dismutase