Inhibition of ethanol-induced toxicity by tanshinone ⅡA in PC12 cells

来源 :Acta Pharmacologica Sinica | 被引量 : 0次 | 上传用户:frankxigua
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Aim:To observe the effects of tanshinone IIA(Tan IIA)on the neurotoxicityinduced by ethanol in PC 12 cells and to explore its protective role.Methods:PC 12cell survival was measured by MTT assay.The formation of reactive oxygenspecies(ROS)and lactate dehydrogenase(LDH)release were detected by 2′,7′-dichlorofluorescin(DCF)fluorescence and calorimetric method,respectively.Thepercentage of cell apoptosis was monitored by flow cytometry.The expression ofp53 was detected by immuno-fluorescence and flow cytometry.Results:Ethanolsignificantly impaired the survival of PC12 cells as demonstrated by MTT assay.Ethanol also induced significant ROS formation and increased LDH release.Pre-incubation with Tan IIA in the culture medium significantly reversed these changes.Ethanol caused cell apoptosis and the upregulation of p53 protein.The anti-apoptosis effects of Tan IIA on ethanol-induced toxicity were accompanied by thedownregulation of pro-apoptotic p53 protein expression.Conclusion:Tan IIAcan protect neurons from apoptosis and might serve as a potential therapeuticdrug for neurological disorders induced by ethanol. Aim: To observe the effects of tanshinone IIA (Tan IIA) on the neurotoxicity induced by ethanol in PC 12 cells and to explore its protective role. Methods: PC 12 cell survival was measured by MTT assay. The formation of reactive oxygenspecies (ROS) and lactate dehydrogenase (LDH) released were detected by 2 ’, 7’-dichlorofluorescin (DCF) fluorescence and calorimetric method, respectively. The percentage of cell apoptosis was monitored by flow cytometry. The expression of p53 was detected by immuno-fluorescence and flow cytometry. Results: Ethanolsignificantly impaired the survival of PC12 cells as demonstrated by MTT assay. Ethanol also induced significant ROS formation and increased LDH release. Pre-incubation with Tan IIA in the culture mediumâ “ƒ” reversed cell changes. Ethanol caused cell apoptosis and the upregulation of p53 protein. The anti-apoptosis effects of Tan IIA on ethanol-induced toxicity were accompanied by the downregulation of pro-apoptotic p53 protein expression. Confluence: Tan II Ac an protect neurons from apoptosis and might serve as a potential therapeutic drug for neurological disorders induced by ethanol.
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