Satratoxin H generates reactive oxygen species and lipid peroxides in PC12 cells

Punnee Nusuetrong1, Thitima Pengsuparp, Duangdeun Meksuriyen

  • 1Department of Physiology, Faculty of Medicine, Srinakharinwirot University, Sukhumvit, Bangkok, Thailand.

Insights

Satratoxin H induces apoptosis in PC12 cells by increasing reactive oxygen species (ROS). Glutathione (GSH) can protect cells, suggesting ROS generation mediates this mycotoxin-induced cell death.

Area of Science:

  • Toxicology
  • Cell Biology
  • Biochemistry

Background:

  • Satratoxin H is a mycotoxin known to induce apoptosis in PC12 cells.
  • Previous studies suggest a role for p38 MAPK and JNK pathways, modulated by glutathione (GSH).

Purpose of the Study:

  • To further elucidate the mechanism of satratoxin H-induced cell death in PC12 cells.
  • To investigate the role of reactive oxygen species (ROS) in satratoxin H toxicity.

Main Methods:

  • PC12 cells were treated with satratoxin H.
  • Apoptosis was assessed via DNA fragmentation and flow cytometry.
  • ROS production and lipid peroxidation (malondialdehyde) were measured.
  • Effects of GSH incubation were evaluated.

Main Results:

  • Satratoxin H induced significant apoptosis in PC12 cells within 24 hours.
  • Increased ROS production and lipid peroxidation were observed following satratoxin H exposure.
  • Incubation with GSH attenuated the satratoxin H-induced apoptosis and ROS generation.

Conclusions:

  • Satratoxin H induces apoptosis in PC12 cells, partly mediated by ROS generation.
  • Glutathione (GSH) plays a protective role against satratoxin H toxicity.
  • The findings highlight the involvement of oxidative stress in satratoxin H-induced cytotoxicity.