2009Journal of Sun Yat-sen UniversityRequires access

Effects of Rifampicin on Rotenone-induced Oxidative Stress in Differentiated PC12 Cells

Enxiang Tao

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Abstract

【Objective】 To explore the effects of rifampicin on cell morphology,intracellular reactive oxygen species(ROS),reduced glutathione(GSH),and cell apoptosis in rotenone-induced differentiated pheochromocytoma(PC12) cells.【Methods】 Rotenone was added in rat PC12 cells to develop a model of Parkinson's disease in vitro.Cell morphology was observed by microscope.Intracellular GSH was determined by a microplate reader.The intracellular ROS and the apoptosis rate were measured by flow cytometry.【Results】 Compared with control group and rifampicin control group,GSH significantly decreased but ROS and apoptosis rate significantly increased in rotenone group.Compared with rotenone group,GSH significantly increased but ROS and apoptosis rate significantly decreased in a dose-dependent manner in rifampicin control group(100,200,and 300 μmol/L).【Conclusion】 Rifampicin may reduce the damage of rotenone-induced differentiated PC12 cells through inhibiting oxidative injury in a dose-dependent manner.

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【Objective】 To explore the effects of rifampicin on cell morphology,intracellular reactive oxygen species(ROS),reduced glutathione(GSH),and cell apoptosis in rotenone-induced differentiated pheochromocytoma(PC12) cells.【Methods】 Rotenone was added in rat PC12 cells to develop a model of Parkinson's disease in vitro.Cell morphology was observed by microscope.Intracellular GSH was determined by a microplate reader.The intracellular ROS and the apoptosis rate were measured by flow cytometry.【Results】 Compared with control group and rifampicin control group,GSH significantly decreased but ROS and apoptosis rate significantly increased in rotenone group.Compared with rotenone group,GSH significantly increased but ROS and apoptosis rate significantly decreased in a dose-dependent manner in rifampicin control group(100,200,and 300 μmol/L).【Conclusion】 Rifampicin may reduce the damage of rotenone-induced differentiated PC12 cells through inhibiting oxidative injury in a dose-dependent manner.

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Available abstract

【Objective】 To explore the effects of rifampicin on cell morphology,intracellular reactive oxygen species(ROS),reduced glutathione(GSH),and cell apoptosis in rotenone-induced differentiated pheochromocytoma(PC12) cells.【Methods】 Rotenone was added in rat PC12 cells to develop a model of Parkinson's disease in vitro.Cell morphology was observed by microscope.Intracellular GSH was determined by a microplate reader.The intracellular ROS and the apoptosis rate were measured by flow cytometry.【Results】 Compared with control group and rifampicin control group,GSH significantly decreased but ROS and apoptosis rate significantly increased in rotenone group.Compared with rotenone group,GSH significantly increased but ROS and apoptosis rate significantly decreased in a dose-dependent manner in rifampicin control group(100,200,and 300 μmol/L).【Conclusion】 Rifampicin may reduce the damage of rotenone-induced differentiated PC12 cells through inhibiting oxidative injury in a dose-dependent manner.

Key concepts: Rotenone, Oxidative stress, Apoptosis, Intracellular, Glutathione, Reactive oxygen species, Flow cytometry, Chemistry

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