Antioxidant Activity and Protective Effects of Tripterygium regelii Extract on Hydrogen Peroxide-Induced Injury in Human Dopaminergic Cells, SH-SY5Y

被引:53
作者
Choi, Bong-Suk [1 ,2 ]
Sapkota, Kumar [1 ]
Kim, Seung [3 ]
Lee, Hyo Jeong [3 ]
Choi, Han-Seok [4 ]
Kim, Sung-Jun [1 ,2 ]
机构
[1] Chosun Univ, Dept Biotechnol, Kwangju 501759, South Korea
[2] Chosun Univ, Res Team Prot Activ Control BK21, Kwangju 501759, South Korea
[3] Gwangju Univ, Dept Alternat Med, Kwangju 503703, South Korea
[4] RDA, Natl Acad Agr Sci, Dept Agrofood Resources, Suwon 441853, South Korea
关键词
Parkinson disease; Tripterygium regelii; Dopaminergic cell; Hydrogen peroxide; Apoptosis; OXIDATIVE STRESS; NEUROTROPHIC FACTOR; TYROSINE-HYDROXYLASE; APOPTOSIS; DEATH; INHIBITION; MECHANISMS; INDUCTION; CELASTROL; NEURONS;
D O I
10.1007/s11064-010-0185-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The present work was conducted to investigate the antioxidant activity and neuroprotective effects of Tripterygium regelii extract (TRE) on H2O2-induced apoptosis in human dopaminergic cells, SH-SY5Y. TRE possessed considerable amounts of phenolics (282.73 mg tannic acid equivalents/g of extract) and flavonoids (101.43 mg naringin equivalents/g of extract). IC50 values for reducing power and DPPH radical scavenging activity were 52.51 and 47.83 mu g, respectively. The H2O2 scavenging capacity of TRE was found to be 57.68 mu M x mu g(-1) min(-1). By examining the effects of TRE on SH-SY5Y cells injured by H2O2, we found that after incubation of cells with TRE prior to H2O2 exposure, the H2O2 induced cytotoxicity was significantly reversed and the apoptotic features such as change in cellular morphology, nuclear condensation and DNA fragmentation was inhibited. Moreover, TRE was very effective attenuating the disruption of mitochondrial membrane potential and apoptotic cell death induced by H2O2. TRE extract effectively suppressed the up-regulation of Bax, Caspase-3 and -9, and down-regulation of Bcl-2. Moreover, TRE pretreatment evidently increased the tyrosine hydroxylase (TH) and brain-derived neurotrophic factor (BDNF) in SH-SY5Y cells. These findings demonstrate that TRE protects SH-SY5Y cells against H2O2-induced injury and antioxidant properties may account for its neuroprotective actions and suggest that TRE might potentially serve as an agent for prevention of neurodegenerative disease associated with oxidative stress.
引用
收藏
页码:1269 / 1280
页数:12
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