Effect of sesaminol glucosides on beta-amyloid-induced PC12 cell death through antioxidant mechanisms

Neurosci Res. 2005 Aug;52(4):330-41. doi: 10.1016/j.neures.2005.04.003.

Abstract

Several lines of evidence support that beta-amyloid (Abeta)-induced neurotoxicity is mediated through the generation of reactive oxygen species (ROS) and elevation of intracellular calcium. In this study, we have investigated protective effects of sesaminol glucosides on Abeta-induced oxidative cell death in cultured rat pheochromocytoma (PC12) cells. Sesaminol glucoside (50-250microg/ml) decreased Abeta(25-35)-induced ROS generation, formation of 8-oxodG, a form of oxidative DNA and elevation of intracellular calcium level concomitant with prevention of apoptotic cell death dose dependently. Sesaminol glucoside (50-250microg/ml) also effectively decreased Abeta1-42 and ADDL form of Abeta1-42 as well as the combination of H2O2 with FeSO4-induced cell damages. In mechanistic study, sesaminol glucosides attenuated Abeta25-35-induced activation of redox transcription factor nuclear factor-kappaB NF-kappaB through inhibition of p50 translocation and IkappaB phosphorylation, and blocked NF-kappaB-dependent luciferase activity in addition to the inhibitory effect on Abeta25-35-induced activation of ERK kinase signal pathway. Consistent with the inhibitory effect on Abeta25-35-induced stress-induced cell death, sesaminol glucosides decreased expression of pro-apoptotic gene p53, and Bax and caspase-3, but enhanced expression of anti-apoptotic Bcl-2. Moreover, the protective effects of sesaminol glucoside on Abeta25-35-induced ROS generation, NF-kappaB activation and cell death were further enhanced with glutathione. This study therefore suggests that sesaminol glucosides have protective effect on Abeta-induced neuronal cell death, and its effect may be through antioxidative property.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • 8-Hydroxy-2'-Deoxyguanosine
  • Amyloid beta-Peptides / toxicity*
  • Animals
  • Antioxidants / pharmacology*
  • Blotting, Western / methods
  • Calcium / metabolism
  • Caspase 3
  • Caspases / metabolism
  • Cell Death / drug effects*
  • Cell Survival / drug effects
  • Deoxyguanosine / analogs & derivatives
  • Deoxyguanosine / metabolism
  • Dioxoles / pharmacology*
  • Dose-Response Relationship, Drug
  • Drug Interactions
  • Electrophoretic Mobility Shift Assay / methods
  • Enzyme-Linked Immunosorbent Assay / methods
  • Furans / pharmacology*
  • Glucosides / pharmacology
  • Humans
  • Hydrogen Peroxide / pharmacology
  • Indoles
  • Iron / pharmacology
  • Mitogen-Activated Protein Kinases / metabolism
  • NF-kappa B / metabolism
  • PC12 Cells / cytology
  • PC12 Cells / drug effects*
  • Peptide Fragments / toxicity*
  • Proto-Oncogene Proteins c-bcl-2 / metabolism
  • RNA, Messenger / biosynthesis
  • Rats
  • Reactive Oxygen Species / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction / methods
  • Sulfides / pharmacology
  • Tetrazolium Salts
  • Thiazoles
  • Tumor Suppressor Protein p53 / metabolism
  • bcl-2-Associated X Protein

Substances

  • Amyloid beta-Peptides
  • Antioxidants
  • BAX protein, human
  • Bax protein, rat
  • Dioxoles
  • Furans
  • Glucosides
  • Indoles
  • NF-kappa B
  • Peptide Fragments
  • Proto-Oncogene Proteins c-bcl-2
  • RNA, Messenger
  • Reactive Oxygen Species
  • Sulfides
  • Tetrazolium Salts
  • Thiazoles
  • Tumor Suppressor Protein p53
  • amyloid beta-protein (1-42)
  • amyloid beta-protein (25-35)
  • bcl-2-Associated X Protein
  • pyrite
  • DAPI
  • sesaminol
  • 8-Hydroxy-2'-Deoxyguanosine
  • Hydrogen Peroxide
  • Iron
  • Mitogen-Activated Protein Kinases
  • CASP3 protein, human
  • Casp3 protein, rat
  • Caspase 3
  • Caspases
  • thiazolyl blue
  • Deoxyguanosine
  • Calcium