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Alpha-synuclein is upregulated in neurones in response to chronic oxidative stress and is associated with neuroprotection
- Source :
- Experimental Neurology. 199:249-256
- Publication Year :
- 2006
- Publisher :
- Elsevier BV, 2006.
-
Abstract
- Chronic oxidative stress has been linked to the neurodegenerative changes characteristic of Parkinson's disease, particularly alpha-synuclein accumulation and aggregation. However, it remains contentious whether these alpha-synuclein changes are cytotoxic or neuroprotective. The current study utilised long-term primary neural culture techniques with antioxidant free media to study the cellular response to chronic oxidative stress. Cells maintained in antioxidant free media were exquisitely more vulnerable to acute exposure to hydrogen peroxide, yet exposure of up to 10 days in antioxidant free media did not lead to morphological alterations in neurones or glia. However, a subpopulation of neurones demonstrated a significant increase in the level of alpha-synuclein expressed within the cell body and at synaptic sites. This subset of neurones was also more resistant to apoptotic changes following exposure to antioxidant free media relative to other neurones. These data indicate that increased alpha-synuclein content is associated with neuroprotection from relatively low levels of oxidative stress.
- Subjects :
- Diagnostic Imaging
Time Factors
Antioxidant
Docosahexaenoic Acids
medicine.medical_treatment
Cell
Cell Count
Pharmacology
medicine.disease_cause
Neuroprotection
R-SNARE Proteins
chemistry.chemical_compound
Developmental Neuroscience
Downregulation and upregulation
Glial Fibrillary Acidic Protein
medicine
Animals
Cytotoxic T cell
Cerebral Cortex
Neurons
Alpha-synuclein
business.industry
Hydrogen Peroxide
Oxidants
Immunohistochemistry
Up-Regulation
Oxidative Stress
medicine.anatomical_structure
nervous system
Neurology
chemistry
Apoptosis
Culture Media, Conditioned
alpha-Synuclein
business
Microtubule-Associated Proteins
Neuroscience
Oxidative stress
Subjects
Details
- ISSN :
- 00144886
- Volume :
- 199
- Database :
- OpenAIRE
- Journal :
- Experimental Neurology
- Accession number :
- edsair.doi.dedup.....1765b3a0bf04fbf1e51b245ba4d22434