4.7 Article Proceedings Paper

Oxidative Stress in Parkinson's Disease A Mechanism of Pathogenic and Therapeutic Significance

出版社

WILEY-BLACKWELL
DOI: 10.1196/annals.1427.023

关键词

Parkinson's disease; oxidative stress; reactive oxygen species

资金

  1. NIA NIH HHS [R01 AG21617, R01 AG021617-05, R01 AG021617] Funding Source: Medline
  2. NINDS NIH HHS [R01 NS042269-05A2, P50 NS38370, R21 NS062180-02, R21 NS064191-01A1, R21 NS064191, R21 NS062180, P01 NS011766, P50 NS038370-100001, R01 NS042269, P01 NS11766-27A1, P50 NS038370] Funding Source: Medline
  3. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [R21NS062180, P01NS011766, R21NS064191, R01NS042269, P50NS038370] Funding Source: NIH RePORTER
  4. NATIONAL INSTITUTE ON AGING [R01AG021617] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Parkinson's disease (PD) is a common adult-onset neurodegenerative disorder. Typically PD is a sporadic neurological disorder, and over time affected patients see their disability growing and their quality of life declining. Oxidative stress has been hypothesized to be linked to both the initiation and the progression of PD. Preclinical findings from both in vitro and in vivo experimental models of PD suggest that the neurodegenerative process starts with otherwise healthy neurons being hit by some etiological factors, which sets into motion a cascade of deleterious events. In these models initial molecular alterations in degenerating dopaminergic neurons include increased formation of reactive oxygen species, presumably originating from both inside and outside the mitochondria. In the 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) mouse model of PD, time-course experiments suggest that oxidative stress is an early event that may directly kill some of the dopaminergic neurons. In this model it seems that oxidative stress may play a greater role in the demise of dopaminergic neurons indirectly by activating intracellular, cell death-related, molecular pathways. As the neurodegenerative process evolves in the MPTP mouse model, indices of neuroinflammation develop, such as microglial activation. The latter increases the level of oxidative stress to which the neighboring compromised neurons are subjected to, thereby promoting their demise. However, these experimental studies have also shown that oxidative stress is not the sole deleterious factor implicated in the death of dopaminergic neurons. Should a similar multifactorial cascade underlie dopaminergic neuron degeneration in PD, then the optimal therapy for this disease may have to rely on a cocktail of agents, each targeting a different critical component of this hypothesized pathogenic cascade. If correct, this may be a reason why neuroprotective trials using a single agent, such as an antioxidant, have thus far generated disappointing results.

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