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

dc.contributor.authorNusuetrong P.
dc.contributor.authorPengsuparp T.
dc.contributor.authorMeksuriyen D.
dc.contributor.authorTanitsu M.
dc.contributor.authorKikuchi H.
dc.contributor.authorMizugaki M.
dc.contributor.authorShimazu K.-I.
dc.contributor.authorOshima Y.
dc.contributor.authorNakahata N.
dc.contributor.authorYoshida M.
dc.date.accessioned2021-04-05T04:31:59Z
dc.date.available2021-04-05T04:31:59Z
dc.date.issued2008
dc.date.issuedBE2551
dc.description.abstractSatratoxin 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.mimetypeapplication/pdf
dc.identifier.citationBiological and Pharmaceutical Bulletin. Vol 31, No.6 (2008), p.1115-1120
dc.identifier.doi10.1248/bpb.31.1115
dc.identifier.issn9186158
dc.identifier.other2-s2.0-45749109056
dc.identifier.urihttps://hdl.handle.net/20.500.14740/4020
dc.rights.holderมหาวิทยาลัยศรีนครินทรวิโรฒ
dc.subject.otherGlutathione
dc.subject.otherLipid peroxide
dc.subject.otherMalonaldehyde
dc.subject.otherMycotoxin
dc.subject.otherReactive oxygen metabolite
dc.subject.otherSatratoxin h
dc.subject.otherAnimal cell
dc.subject.otherApoptosis
dc.subject.otherArticle
dc.subject.otherCell viability
dc.subject.otherControlled study
dc.subject.otherDNA fragmentation
dc.subject.otherDrug effect
dc.subject.otherDrug mechanism
dc.subject.otherFlow cytometry
dc.subject.otherLipid peroxidation
dc.subject.otherNonhuman
dc.subject.otherPheochromocytoma
dc.subject.otherRat
dc.subject.otherAnimals
dc.subject.otherAntioxidants
dc.subject.otherCell Survival
dc.subject.otherDNA Fragmentation
dc.subject.otherElectrophoresis, Agar Gel
dc.subject.otherFlow Cytometry
dc.subject.otherG1 Phase
dc.subject.otherGlutathione
dc.subject.otherIndicators and Reagents
dc.subject.otherJNK Mitogen-Activated Protein Kinases
dc.subject.otherLipid Peroxidation
dc.subject.otherP38 Mitogen-Activated Protein Kinases
dc.subject.otherPC12 Cells
dc.subject.otherRats
dc.subject.otherReactive Oxygen Species
dc.subject.otherThiobarbituric Acid Reactive Substances
dc.subject.otherTrichothecenes
dc.titleSatratoxin H generates reactive oxygen species and lipid peroxides in PC12 cells
dc.typeArticle
dspace.entity.typePublication
swu.datasource.scopushttps://www.scopus.com/inward/record.uri?eid=2-s2.0-45749109056&doi=10.1248%2fbpb.31.1115&partnerID=40&md5=e1e4a9d282e4055287d49b2a3ecb96ee

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