Abstract |
The present study was designed to investigate the potential neuroprotective effect of ω- conotoxin (ω-CTX) in a cell-based model of Alzheimer's disease (AD) using cultured PC12 cells incubated with β- amyloid (Aβ). Immunohistochemical staining, Western blot, MTT and TdT-mediated dUTP- biotin nick end labeling (TUNEL) analysis were employed to assess the cell viability and cell death. Aβ in this model was clearly neurotoxic, inducing necrosis and apoptosis. ω-CTX antagonized the effects of Aβ: there was an increase in cell viability and a suppression of inflammatory- and oxidative stress-related factors. These data suggest that ω-CTX may have neuroprotective actions against Aβ-induced neurotoxicity. The significance of these new findings relative to the etiology and treatment of AD is discussed.
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Authors | Marong Fang, Jing Wang, Shu Han, Zhiying Hu, Jin-biao Zhan, Shucai Ling, John A Rudd, Yu Geng |
Journal | Toxicology letters
(Toxicol Lett)
Vol. 206
Issue 3
Pg. 325-38
(Oct 30 2011)
ISSN: 1879-3169 [Electronic] Netherlands |
PMID | 21839817
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2011 Elsevier Ireland Ltd. All rights reserved. |
Chemical References |
- Amyloid beta-Peptides
- Bax protein, rat
- Neuroprotective Agents
- Proto-Oncogene Proteins c-bcl-2
- bcl-2-Associated X Protein
- omega-Conotoxins
- Caspase 3
- Trypan Blue
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Topics |
- Amyloid beta-Peptides
(toxicity)
- Animals
- Apoptosis
(drug effects)
- Caspase 3
(metabolism)
- Cell Survival
(drug effects)
- Dose-Response Relationship, Drug
- Immunohistochemistry
- Microscopy, Phase-Contrast
- Neuroprotective Agents
(pharmacology)
- Oxidative Stress
(drug effects)
- PC12 Cells
- Proto-Oncogene Proteins c-bcl-2
(analysis)
- Rats
- Trypan Blue
(metabolism)
- bcl-2-Associated X Protein
(analysis)
- omega-Conotoxins
(pharmacology)
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