Effects of sericin on oxidative stress and PI3K/AKT/mTOR signal pathway in cryopreserved mice ovarian tissue

Cryobiology. 2023 Jun:111:16-25. doi: 10.1016/j.cryobiol.2023.03.003. Epub 2023 Mar 17.

Abstract

Ovarian tissue cryopreservation is an effective fertility protective strategy for preadolescent female cancer patients, whose tumor treatment cannot be delayed. In the present study, the effects of sericin, as an antioxidant, on mice ovarian tissue freezing and thawing were investigated. Mice ovarian tissues were cryopreserved and thawed in medium containing 0.5% or 1%sericin (w/v), and 0.1 mM melatonin. Then, the follicular morphology was observed. The levels of antioxidant enzymes were determined, including glutathione (GSH), glutathione peroxidase (GSH-Px), total superoxide dismutase (T-SOD), total antioxidant capacity (T-AOC) and catalase (CAT). Moreover, the levels of nitric oxide (NO), malondialdehyde (MDA) and lactate dehydrogenase (LDH) were also tested. Besides, apoptosis-related proteins Bcl-2 and Bax were determined. Our results showed that 1% sericin maintained follicular morphology, inhibited apoptosis, decreased MDA and NO levels, and boosted endogenous antioxidant enzyme levels, while had no significant effect on LDH levels. Furthermore, these effects may be related with the activation of the phosphatidylinositol-3-kinase (PI3K)/protein kinase B (AKT)/mammalian target of Rapamycin (mTOR) signaling pathway, as demonstrated by increased PI3K, p-AKT and mTOR levels. These findings demonstrate that 1% sericin may reduce oxidative stress and protect ovarian tissues during freezing and thawing via PI3K/AKT/mTOR signaling pathway.

Keywords: Antioxidant; Ovarian tissue cryopreservation; PI3K/AKT/mTOR signaling pathway; Sericin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antioxidants / metabolism
  • Antioxidants / pharmacology
  • Apoptosis
  • Cryopreservation / methods
  • Female
  • Glutathione / pharmacology
  • Mammals / metabolism
  • Mice
  • Oxidative Stress
  • Phosphatidylinositol 3-Kinase / metabolism
  • Phosphatidylinositol 3-Kinase / pharmacology
  • Phosphatidylinositol 3-Kinases / metabolism
  • Phosphatidylinositol 3-Kinases / pharmacology
  • Proto-Oncogene Proteins c-akt* / metabolism
  • Sericins* / pharmacology
  • Signal Transduction
  • TOR Serine-Threonine Kinases / metabolism
  • TOR Serine-Threonine Kinases / pharmacology

Substances

  • Proto-Oncogene Proteins c-akt
  • Phosphatidylinositol 3-Kinase
  • Phosphatidylinositol 3-Kinases
  • Sericins
  • Antioxidants
  • TOR Serine-Threonine Kinases
  • Glutathione