Related Experiment Video
Updated: Nov 20, 2025

Author Spotlight: Investigating the Mechanisms and Inducing Models of Polycystic Ovary Syndrome
Published on: July 5, 2024
[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.
Abstract:
The aim of this paper was to study the role of phosphoinositide 3-kinase(PI3 K), protein kinase B(Akt) and mamma-lian target of rapamycin(mTOR) in the inhibition of premature ovarian failure induced by D-galactose(D-gal) in mice model by ginsenoside Rg_1(Rg_1). Fifty-four female SPF BALB/c mice were randomly divided into PBS group, D-gal group, and Rg_1 group. In the D-gal group, D-galactose(200 mg·kg~(-1)·d~(-1)) was injected subcutaneously into the neck and back for 42 days. In the PBS group, an equal amount of phosphate buffered saline(PBS) was injected into the neck and back for 42 days. In addition to the therapy of D-gal group, Rg_1 group was given Rg_1(20 mg·kg~(-1)·d~(-1)) through intraperitoneal injection since the 15 th day for 28 days, at the same time, the D-gal group and the PBS group were also given an equal amount of PBS through intraperitoneal injection since the 15 th day for 28 days. After the treatment, the estrous cycle changes of the mice were detected, and the ovarian SA-β-Gal staining was used to detect the changes of ovarian aging. Western blot was used to detect the changes in protein expressions of PI3 K, Akt, mTOR, S6 k, LC3-Ⅱ and P16~(INK4 a). Fluorescence quantitative PCR was used to detect the changes in mRNA expressions of PI3 K, Akt, mTOR, S6 k, LC3-Ⅱ and P16~(INK4 a). According to the findings, compared with the PBS group, the D-gal group began to show estrous cycle disorder in the 3 rd week,the ovarian SA-β-Gal staining positive granulosa cells increased in the D-gal group, the expression of senescence marker P16~(INK4 a) increased, while the expression of autophagy signaling molecule LC3-Ⅱ decreased. After treatment with Rg_1, the positive rate of ovarian SA-β-Gal staining in Rg_1 group decreased, the expression level of autophagy signaling molecule LC3-Ⅱ in Rg_1 group was higher than that in D-gal group, while the expression level of senescence marker P16~(INK4 a) was lower than that in D-gal group. Compared with the PBS group, the protein and mRNA expressions of PI3 K, Akt, mTOR and S6 k in the D-gal group were up-regulated, the protein expressions of Akt, mTOR and S6 k in the Rg_1 group were up-regulated, and the mRNA expressions of PI3 K and mTOR were up-regulated. After treatment with Rg_1, the protein expressions of PI3 K, Akt, mTOR and S6 k in the Rg_1 group were lower than those in the D-gal group, while the mRNA expressions of Akt, mTOR and S6 k in the Rg_1 group were lower than those in the D-gal group. The finding ssuggested that Rg_1 has the effect in delaying ovarian premature failure in D-gal-induced mouse models, and PI3 K/Akt/mTOR autophagy signaling pathways play an important role.
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.
More Related Videos
06:49Orthotopic Ovarian Transplantation Procedures to Investigate the Life- and Health-span Influence of Ovarian Senescence in Female Mice
Published on: February 12, 2018
06:18An In Vivo Estrogen Deficiency Mouse Model for Screening Exogenous Estrogen Treatments of Cardiovascular Dysfunction After Menopause
Published on: August 13, 2019
Related Concept Videos
PI3K/mTOR/AKT Signaling Pathway
mTOR Signaling and Cancer Progression
The mTOR pathway or the...