Melatonin prevents the dynamin-related protein 1-dependent mitochondrial fission and oxidative insult in the cortical neurons after 1-methyl-4-phenylpyridinium treatment

作者：Chuang Jih Ing^*; Pan I Ling; Hsieh Chia Yun; Huang Chiu Ying; Chen Pei Chun; Shin Jyh Wei

来源：Journal of Pineal Research, 2016, 61(2): 230-240.

DOI：10.1111/jpi.12343

• dynamin-related protein 1
• melatonin
• mitochondrial fission
• oxidative stress
• Parkinson's diseases

Mitochondrial dysfunction and oxidative stress are involved in the pathogenesis of Parkinson's disease (PD). Mitochondrial morphology is dynamic and precisely regulated by the mitochondrial fission and fusion machinery. Aberrant mitochondrial fragmentation controlled by the mitochondrial fission protein, dynamin-related protein 1 (Drp1), may result in cell death. Our previous results showed that melatonin protected neurons by inhibiting oxidative stress in a 1-methyl-4-phenylpyridinium (MPP+)-induced PD model. However, the effect of melatonin on mitochondrial dynamics remains uncharacterized. Herein, we investigated the effect of melatonin and the role of Drp1 on MPP+-induced mitochondrial fission in rat primary cortical neurons. We found that MPP+ induced a rapid increase in the ratio of GSSG:total glutathione (a marker of oxidative stress) and mitochondrial fragmentation, Drp1 upregulation within 4hours, and finally resulted in neuron loss 48hours after the treatment. Neurons overexpressing wild-type Drp1 promoted mitochondrial and nuclear fragmentation; however, neurons overexpressing dominant-negative Drp1(K38A) or cotreated with melatonin exhibited significantly reduced MPP+-induced mitochondrial fragmentation and neuron death. Moreover, melatonin cotreatment prevented an MPP+-induced high ratio of GSSG and mitochondrial Drp1 upregulation. The prevention of mitochondrial fission by melatonin was not found in neurons transfected with wild-type Drp1. These results provide a new insight that the neuroprotective effect of melatonin against MPP+ toxicity is mediated by inhibiting the oxidative stress and Drp1-mediated mitochondrial fragmentation.

• 出版日期2016-9