Resveratrol Plays a Protective Role against Premature Ovarian Failure and Prompts Female Germline Stem Cell Survival

Int J Mol Sci. 2019 Jul 23;20(14):3605. doi: 10.3390/ijms20143605.

Abstract

This study was designed to investigate the protective effect of resveratrol (RES) on premature ovarian failure (POF) and the proliferation of female germline stem cells (FGSCs) at the tissue and cell levels. POF mice were lavaged with RES, and POF ovaries were co-cultured with RES and/or GANT61 in vitro. FGSCs were pretreated with Busulfan and RES and/or GANT61 and co-cultured with M1 macrophages, which were pretreated with RES. The weights of mice and their ovaries, as well as their follicle number, were measured. Ovarian function, antioxidative stress, inflammation, and FGSCs survival were evaluated. RES significantly increased the weights of POF mice and their ovaries as well as the number of follicles, while it decreased the atresia rate of follicles. Higher levels of Mvh, Oct4, SOD2, GPx, and CAT were detected after treatment with RES in vivo and in vitro. RES treatment resulted in significantly lower TNF-α and IL-6 concentrations and an obviously higher IL-10 concentration in the ovaries. In FGSCs, higher Mvh, Oct4, and SOD2 concentrations and lower TNF-α, IL-6, and MDA concentrations were measured in the RES group. Blockage of the Hh signaling pathway reversed the protective effect of RES on FGSCs. In conclusion, RES effectively improved the ovarian function of the POF model and the productive capacity of FGSCs via relieving oxidative stress and inflammation and a mechanism involving the Hh signaling pathway, suggesting that RES is a potential agent against POF and can aid in the survival of FGSCs.

Keywords: female germline stem cells; hedgehog; inflammation; oxidative stress; premature ovarian failure; resveratrol.

MeSH terms

  • Animals
  • Antioxidants / pharmacology*
  • Body Weight / drug effects
  • Busulfan / toxicity
  • Catalase / genetics
  • Catalase / metabolism
  • Cell Survival / drug effects
  • Coculture Techniques
  • DEAD-box RNA Helicases / genetics
  • DEAD-box RNA Helicases / metabolism
  • Female
  • Gene Expression Regulation / drug effects*
  • Glutathione Peroxidase / genetics
  • Glutathione Peroxidase / metabolism
  • Glutathione Peroxidase GPX1
  • Humans
  • Interleukin-6 / genetics
  • Interleukin-6 / metabolism
  • Macrophages / cytology
  • Macrophages / drug effects
  • Macrophages / metabolism
  • Mice
  • Octamer Transcription Factor-3 / genetics
  • Octamer Transcription Factor-3 / metabolism
  • Oogonial Stem Cells / drug effects*
  • Oogonial Stem Cells / metabolism
  • Oogonial Stem Cells / pathology
  • Organ Size / drug effects
  • Ovarian Follicle / drug effects*
  • Ovarian Follicle / metabolism
  • Ovarian Follicle / pathology
  • Primary Cell Culture
  • Primary Ovarian Insufficiency / chemically induced
  • Primary Ovarian Insufficiency / drug therapy*
  • Primary Ovarian Insufficiency / genetics
  • Primary Ovarian Insufficiency / pathology
  • Pyridines / antagonists & inhibitors
  • Pyridines / pharmacology
  • Pyrimidines / antagonists & inhibitors
  • Pyrimidines / pharmacology
  • Resveratrol / pharmacology*
  • Signal Transduction
  • Superoxide Dismutase / genetics
  • Superoxide Dismutase / metabolism
  • Tumor Necrosis Factor-alpha / genetics
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Antioxidants
  • GANT 61
  • Interleukin-6
  • Octamer Transcription Factor-3
  • Pou5f1 protein, mouse
  • Pyridines
  • Pyrimidines
  • Tumor Necrosis Factor-alpha
  • interleukin-6, mouse
  • Catalase
  • Glutathione Peroxidase
  • Superoxide Dismutase
  • superoxide dismutase 2
  • Ddx4 protein, mouse
  • DEAD-box RNA Helicases
  • Busulfan
  • Resveratrol
  • Glutathione Peroxidase GPX1