Abstract:
:There is evidence to support that oxidative stress is increased in Parkinson's disease (PD) and contributes to the degeneration of dopaminergic neurons. Recent research has shown that higher blood urate concentrations have now been linked to decreased risks and progression rates of PD. However, the mechanisms about urate to protect dopaminergic neurons are less clear. Our study investigated the effect of urate on oxidative stress induced by 6-hydroxydopamine (6-OHDA) in neuronal differentiated PC12 cells. We found that urate significantly reduced 6-OHDA-induced lactate dehydrogenas (LDH), malondialdehyde (MDA), and 8-hydroxy-deoxyguanosine (8-OHdG) generation but increased the superoxide dismutase (SOD) activity and glutathione (GSH) levels in the PC12 cells. These results suggested that urate can prevent PC12 cells from oxidative injury induced by 6-OHDA, which may play an important role in the mechanisms underlying the association of high plasma levels of urate with reduced risk and slower progression of PD. Urate treatment could be a potential therapeutic strategy for PD.
journal_name
Neurosci Lettjournal_title
Neuroscience lettersauthors
Zhu TG,Wang XX,Luo WF,Zhang QL,Huang TT,Xu XS,Liu CFdoi
10.1016/j.neulet.2011.10.075subject
Has Abstractpub_date
2012-01-11 00:00:00pages
175-9issue
2eissn
0304-3940issn
1872-7972pii
S0304-3940(11)01487-Xjournal_volume
506pub_type
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