3-O-Demethylswertipunicoside Protects against Oxidative Toxicity in PC12 Cells

被引:13
作者
Zhang, Shi-Ping [1 ,2 ]
Du, Xin-Gang [3 ]
Pu, Xiao-Ping [1 ,2 ]
机构
[1] Peking Univ, State Key Lab Nat & Biomimet Drugs, Beijing 100191, Peoples R China
[2] Peking Univ, Dept Mol & Cellular Pharmacol, Beijing 100191, Peoples R China
[3] Peking Univ, Dept Nat Drugs, Sch Pharmaceut Sci, Beijing 100191, Peoples R China
基金
中国国家自然科学基金;
关键词
3-O-demethylswertipunicoside; neuroprotection; PC; 12; cell; 1-methyl-4-phenylpyridinium ion; tyrosine hydroxylase; DJ-1; TYROSINE-HYDROXYLASE; PARKINSONS-DISEASE; 1-METHYL-4-PHENYLPYRIDINIUM ION; DOPAMINERGIC-NEURONS; PROTOCATECHUIC ACID; HYDROGEN-PEROXIDE; SUBSTANTIA-NIGRA; SWERTIA-PUNICEA; MPTP MODEL; IN-VITRO;
D O I
10.1248/bpb.33.1529
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Xanthone compounds have been reported to inhibit cancer cell growth as well as possessing antioxidant properties. The xanthone compound 3-O-demethylswertipunicoside (3-ODS), extracted from Swertia punicea HEMSL, has not previously been demonstrated to have clear neuroprotective effects. In our study, the 3-(4,5-di-methylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) cell death assay revealed that treatment of PC12 cells with 3-ODS ameliorated the decreased cell viability induced by exposure to 1-methyl-4-phenylpyridinium ion (M PP), rotenone or H2O2. The acridine orange/ethidium bromide (AO/EB) apoptosis assay demonstrated a significant suppression of cell death in PC12 cells. by 3-ODS treatment. 3-ODS increased the protein expression of both tyrosine hydroxylase (TH) and DJ-1 expression in PC12 cells. The current study demonstrates that 3-ODS has potential neuroprotective effects mediated via the elevation of TH and DJ-1 protein levels.
引用
收藏
页码:1529 / 1533
页数:5
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