3-O-Demethylswertipunicoside Protects against Oxidative Toxicity in PC12 Cells
スポンサーリンク
概要
- 論文の詳細を見る
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-dimethylthiazol-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 (MPP+), 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.
著者
-
Zhang Shi-Ping
State Key Laboratory of Natural and Biomimetic Drugs, Peking University
-
Du Xin-Gang
Department of Natural Drugs, School of Pharmaceutical Science, Peking University
-
Pu Xiao-Ping
State Key Laboratory of Natural and Biomimetic Drugs, Peking University
-
Pu Xiao-ping
Dep. Of Molecular And Cellular Pharmacology Peking Univ.
-
Zhang Shi-ping
State Key Lab. Of Natural And Biomimetic Drugs Peking Univ.
関連論文
- 3-O-Demethylswertipunicoside Protects against Oxidative Toxicity in PC12 Cells
- Expression of the Parkinsons Disease-Related Protein DJ-1 during Neural Stem Cell Proliferation
- Synthesis Neutral Rare Earth Complexes of Diethylenetriamine-N,N"-bis(acetyl-isoniazid)-N,N',N"-triacetic Acid as Potential Contrast Enhancement Agents for Magnetic Resonance Imaging
- Synthesis, Thermodynamics Stability Constant and Relaxation Properties of Neutral Gd(III) Complex with Derivative from Diethylene Triamine Pentaacetic Acid and p-Hydroxybenzoyl Hydrazine
- Protocatechuic Acid Inhibits Rat Pheochromocytoma Cell Damage Induced by a Dopaminergic Neurotoxin