Protective Effects of Resveratrol and Quercetin Against MPP+ -Induced Oxidative Stress Act by Modulating Markers of Apoptotic Death in Dopaminergic Neurons

被引:162
作者
Bournival, Julie [1 ,2 ]
Quessy, Patrik [1 ,2 ]
Martinoli, Maria-Grazia [1 ,2 ,3 ]
机构
[1] Univ Quebec Trois Rivieres, Neurosci Res Grp, Trois Rivieres, PQ G9A 5H7, Canada
[2] Univ Quebec Trois Rivieres, Dept Biochem, Trois Rivieres, PQ G9A 5H7, Canada
[3] Univ Laval, Ctr Rech, Neurosci Res Ctr, Ste Foy, PQ G1V 4G2, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Apoptosis; Resveratrol; Quercetin; Neuroprotection; Oxidative stress; NERVE GROWTH-FACTOR; PARKINSONS-DISEASE; PC12; CELLS; NEUROBLASTOMA-CELLS; GENE-EXPRESSION; MESENCEPHALIC CULTURES; TYROSINE-HYDROXYLASE; ALZHEIMERS-DISEASE; ESTROGEN-RECEPTORS; DNA FRAGMENTATION;
D O I
10.1007/s10571-009-9411-5
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Reactive oxygen species produced by oxidative stress may participate in the apoptotic death of dopamine neurons distinctive of Parkinson's disease. Resveratrol, a red wine extract, and quercetin, found mainly in green tea, are two natural polyphenols, presenting antioxidant properties in a variety of cellular paradigms. The aim of this study was to evaluate the effect of resveratrol and quercetin on the apoptotic cascade induced by the administration of 1-methyl-4-phenylpyridinium ion (MPP+), a Parkinsonian toxin, provoking the selective degeneration of dopaminergic neurons. Our results show that a pre-treatment for 3 h with resveratrol or quercetin before MPP+ administration could greatly reduce apoptotic neuronal PC12 death induced by MPP+. We also demonstrated that resveratrol or quercetin modulates mRNA levels and protein expression of Bax, a pro-apoptotic gene, and Bcl-2, an anti-apoptotic gene. We then evaluated the release of cytochrome c and the nuclear translocation of the apoptosis-inducing factor (AIF). Altogether, our results indicate that resveratrol and quercetin diminish apoptotic neuronal cell death by acting on the expression of pro- and anti-apoptotic genes. These findings support the role of these natural polyphenols in preventive and/or complementary therapies for several human neurodegenerative diseases caused by oxidative stress and apoptosis.
引用
收藏
页码:1169 / 1180
页数:12
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