Publication: Satratoxin H generates reactive oxygen species and lipid peroxides in PC12 cells
| dc.contributor.author | Nusuetrong P. | |
| dc.contributor.author | Pengsuparp T. | |
| dc.contributor.author | Meksuriyen D. | |
| dc.contributor.author | Tanitsu M. | |
| dc.contributor.author | Kikuchi H. | |
| dc.contributor.author | Mizugaki M. | |
| dc.contributor.author | Shimazu K.-I. | |
| dc.contributor.author | Oshima Y. | |
| dc.contributor.author | Nakahata N. | |
| dc.contributor.author | Yoshida M. | |
| dc.date.accessioned | 2021-04-05T04:31:59Z | |
| dc.date.available | 2021-04-05T04:31:59Z | |
| dc.date.issued | 2008 | |
| dc.date.issuedBE | 2551 | |
| dc.description.abstract | Satratoxin H, a mycotoxin, is thought to induce apoptosis of PC12 cells through the activation of p38 mitogen-activated protein kinase (MAPK) and c-Jun N-terminal kinase (JNK) in a glutathione (GSH)-sensitive manner. The present study was undertaken to further elucidate the mechanism by which satratoxin H induces cell death in PC12 cells. Satratoxin H caused apoptosis of PC12 cells within 24-h, as determined by DNA fragmentation and flow cytometric analysis. Satratoxin H increased reactive oxygen species (ROS) production and lipid peroxidation, as determined by malondialdehyde formation. These effects were attenuated by incubation of cells with GSH, suggesting that satratoxin H-induced increase in apoptosis of serum-deprived PC12 cells may be partially mediated through the generation of ROS. © 2008 Pharmaceutical Society of Japan. | |
| dc.format.mimetype | application/pdf | |
| dc.identifier.citation | Biological and Pharmaceutical Bulletin. Vol 31, No.6 (2008), p.1115-1120 | |
| dc.identifier.doi | 10.1248/bpb.31.1115 | |
| dc.identifier.issn | 9186158 | |
| dc.identifier.other | 2-s2.0-45749109056 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.14740/4020 | |
| dc.rights.holder | มหาวิทยาลัยศรีนครินทรวิโรฒ | |
| dc.subject.other | Glutathione | |
| dc.subject.other | Lipid peroxide | |
| dc.subject.other | Malonaldehyde | |
| dc.subject.other | Mycotoxin | |
| dc.subject.other | Reactive oxygen metabolite | |
| dc.subject.other | Satratoxin h | |
| dc.subject.other | Animal cell | |
| dc.subject.other | Apoptosis | |
| dc.subject.other | Article | |
| dc.subject.other | Cell viability | |
| dc.subject.other | Controlled study | |
| dc.subject.other | DNA fragmentation | |
| dc.subject.other | Drug effect | |
| dc.subject.other | Drug mechanism | |
| dc.subject.other | Flow cytometry | |
| dc.subject.other | Lipid peroxidation | |
| dc.subject.other | Nonhuman | |
| dc.subject.other | Pheochromocytoma | |
| dc.subject.other | Rat | |
| dc.subject.other | Animals | |
| dc.subject.other | Antioxidants | |
| dc.subject.other | Cell Survival | |
| dc.subject.other | DNA Fragmentation | |
| dc.subject.other | Electrophoresis, Agar Gel | |
| dc.subject.other | Flow Cytometry | |
| dc.subject.other | G1 Phase | |
| dc.subject.other | Glutathione | |
| dc.subject.other | Indicators and Reagents | |
| dc.subject.other | JNK Mitogen-Activated Protein Kinases | |
| dc.subject.other | Lipid Peroxidation | |
| dc.subject.other | P38 Mitogen-Activated Protein Kinases | |
| dc.subject.other | PC12 Cells | |
| dc.subject.other | Rats | |
| dc.subject.other | Reactive Oxygen Species | |
| dc.subject.other | Thiobarbituric Acid Reactive Substances | |
| dc.subject.other | Trichothecenes | |
| dc.title | Satratoxin H generates reactive oxygen species and lipid peroxides in PC12 cells | |
| dc.type | Article | |
| dspace.entity.type | Publication | |
| swu.datasource.scopus | https://www.scopus.com/inward/record.uri?eid=2-s2.0-45749109056&doi=10.1248%2fbpb.31.1115&partnerID=40&md5=e1e4a9d282e4055287d49b2a3ecb96ee |
