Acrylamide impairs the developmental potential of germinal vesicle oocytes by inducing mitochondrial dysfunction and

Ji-Guang Gao1,2, Jian-Ke Yang2, Lei Zhu3

  • 112514Life Science College of Anhui Normal University, Provincial Key Lab. of the Conservation and Exploitation Research of Biological Resources in Anhui, Wuhu, China.

Insights

Acrylamide exposure harms mouse oocyte quality by disrupting mitochondrial function, actin assembly, and promoting autophagy and apoptosis. This impacts fertility and early embryo development.

Area of Science:

  • Reproductive toxicology
  • Cellular and molecular biology
  • Environmental health

Background:

  • Acrylamide (ACR) is an endogenous contaminant found in carbohydrate-rich foods.
  • ACR negatively affects multiple organ systems, including the reproductive system.
  • Previous research indicates ACR impairs oocyte quality and fertility.

Purpose of the Study:

  • To investigate the toxic effects of ACR on mouse germinal vesicle (GV) oocytes.
  • To elucidate the regulatory mechanisms underlying ACR-induced oocyte damage.
  • To assess ACR's impact on oocyte mitochondrial function, autophagy, apoptosis, and developmental potential.

Main Methods:

  • Adult female mice were exposed to ACR (10 mg/kg/day) for 4 weeks.
  • GV oocytes were analyzed for mitochondrial function, autophagy/apoptosis markers, and developmental potential.
  • Key gene expression related to autophagy and apoptosis was quantified.

Main Results:

  • ACR exposure reduced oocyte diameter, sperm binding, parthenogenetic activation, and in vitro fertilization (IVF) rates.
  • ACR disrupted oocyte chromatin, mitochondrial distribution, membrane potential, and actin filament expression.
  • Increased LC3 signals, apoptosis rates, and aberrant mRNA expression of autophagy-related genes (ATG3, ATG5, LC3, Beclin1) and mTOR were observed.

Conclusions:

  • ACR exposure significantly impairs the developmental potential of GV oocytes.
  • Mechanisms include induced mitochondrial dysfunction, impaired actin filament assembly, and dysregulated autophagy/apoptosis pathways.
  • These findings highlight ACR as a reproductive toxicant affecting female fertility.