Abstract
Parkinson’s disease (PD) is a common neurodegenerative disorder that primarily afflicts the elderly. It is characterized by motor dysfunction due to extensive neuron loss in the substantia nigra pars compacta. There are multiple biological processes that are negatively impacted during the pathogenesis of PD, and are implicated in the cell death in this region. Neuroinflammation is evidently involved in PD pathology and mitigating the inflammatory cascade has been a therapeutic strategy. Age is the number one risk factor for PD and thus needs to be considered in the context of disease pathology. Here, we discuss the role of neuroinflammation within the context of aging as it applies to the development of PD, and the potential for two representative compounds, fractalkine and astaxanthin, to attenuate the pathophysiology that modulates neurodegeneration that occurs in Parkinson’s disease.
Original language | English |
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Article number | 41 |
Journal | Brain Sciences |
Volume | 6 |
Issue number | 4 |
DOIs | |
State | Published - Dec 2016 |
Bibliographical note
Publisher Copyright:© 2016 by the authors; licensee MDPI, Basel, Switzerland.
Keywords
- Astaxanthin
- Fractalkine
- Microglia
- Neuroinflammation
- Parkinson’s disease
ASJC Scopus subject areas
- General Neuroscience