In this study, the authors used lentiviral vectors to investigated the protective effect of SIRT3 for Parkinson’s disease (PD) cell model. They observe that SIRT3 knockdown significantly worsen rotenone-induced decline of cell viability and enhanced cell apoptosis, exacerbated the decrease of SOD and GSH, and augmented the accumulation of α-synuclein. While SIRT3 overexpression dramatically increased cell viability, and decreased cell apoptosis, prevented the accumulation of α-synuclein, suppressed the reducing of SOD and GSH, decreased ROS generation. These results show that SIRT3 has neuroprotective effect in PD cell model and suggest that it could be developed into a therapeutic agent for PD patients.
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In this study, the authors used lentiviral vectors to investigated the protective effect of SIRT3 for Parkinson’s disease (PD) cell model. They observe that SIRT3 knockdown significantly worsen rotenone-induced decline of cell viability and enhanced cell apoptosis, exacerbated the decrease of SOD and GSH, and augmented the accumulation of α-synuclein. While SIRT3 overexpression dramatically increased cell viability, and decreased cell apoptosis, prevented the accumulation of α-synuclein, suppressed the reducing of SOD and GSH, decreased ROS generation. These results show that SIRT3 has neuroprotective effect in PD cell model and suggest that it could be developed into a therapeutic agent for PD patients.