[Effect of ginsenoside Rg_1 in delaying premature ovarian failure induced by D-gal in mice through PI3K/Akt/mTOR

Xiao-Hu Liu1, Zhi-Hui Zhao1, Yue Zhou1

  • 1Department of Histology and Embryology, School of Basic Medical Sciences, Dali University Dali 671000, China.

Insights

Ginsenoside Rg_1 delays premature ovarian failure in a D-galactose mouse model by modulating the PI3K/Akt/mTOR pathway. This study reveals Rg_1’s potential to combat ovarian aging and supports the role of this signaling pathway in reproductive health.

Area of Science:

  • Reproductive biology and endocrinology
  • Cellular senescence and aging
  • Pharmacology and natural product research

Background:

  • Premature ovarian failure (POF) is a significant reproductive health concern.
  • D-galactose (D-gal) administration is a common method to induce an aging phenotype in animal models.
  • Ginsenoside Rg_1 (Rg_1) is a natural compound with potential therapeutic properties.

Purpose of the Study:

  • To investigate the protective role of Rg_1 against D-gal-induced POF in mice.
  • To elucidate the involvement of the phosphoinositide 3-kinase (PI3K)/protein kinase B (Akt)/mammalian target of rapamycin (mTOR) signaling pathway in this process.
  • To assess the impact of Rg_1 on ovarian aging markers and autophagy.

Main Methods:

  • Establishment of a D-gal-induced POF mouse model.
  • Treatment with Rg_1 and assessment of estrous cycle and ovarian aging (SA-β-Gal staining).
  • Analysis of protein and mRNA expression levels of key signaling molecules (PI3K, Akt, mTOR, S6K, LC3-II, P16INK4a) using Western blot and qPCR.

Main Results:

  • D-gal administration induced estrous cycle disorder, increased ovarian senescence (SA-β-Gal positive cells, P16INK4a expression), and decreased autophagy (LC3-II expression).
  • Rg_1 treatment reversed these D-gal-induced changes, reducing SA-β-Gal staining and P16INK4a levels while increasing LC3-II expression.
  • The PI3K/Akt/mTOR/S6K pathway was upregulated in D-gal-treated mice and modulated by Rg_1, suggesting its role in the observed effects.

Conclusions:

  • Ginsenoside Rg_1 demonstrates a protective effect against D-galactose-induced premature ovarian failure in mice.
  • The PI3K/Akt/mTOR signaling pathway, potentially through its regulation of autophagy and senescence, plays a crucial role in D-gal-induced ovarian aging.
  • Rg_1 may exert its beneficial effects by modulating this critical signaling pathway, offering a potential therapeutic strategy for ovarian aging.