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Melatonin regulates mitochondrial dynamics and alleviates neuron damage in prion diseases

机译:褪黑素调节病毒疾病中的线粒体动力学并减轻神经元损伤

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摘要

Prion diseases are neurodegenerative diseases associated with neuron damage and behavioral disorders in animals and humans. Melatonin is a potent antioxidant and is used to treat a variety of diseases. We investigated the neuroprotective effect of melatonin on prion-induced damage in N2a cells. N2a cells were pretreated with 10 μM melatonin for 1 hour followed by incubation with 100 μM PrP for 24 hours. Melatonin markedly alleviated PrP -induced apoptosis of N2a cells, and inhibited PrP -induced mitochondrial abnormality and dysfunction, including mitochondrial fragmentation and overproduction of reactive oxygen species (ROS), suppression of ATP, reduced mitochondrial membrane potential (MMP), and altered mitochondrial dynamic proteins dynamin-related protein 1 (DRP1) and optic atrophy protein 1 (OPA1). Our findings identify that pretreatment with melatonin prevents the deleterious effects of PrPSc on mitochondrial function and dynamics, protects synapses and alleviates neuron damage. Melatonin could be a novel and effective medication in the therapy of prion diseases.
机译:on病毒是与动物和人类的神经元损害和行为障碍有关的神经退行性疾病。褪黑激素是一种有效的抗氧化剂,可用于治疗多种疾病。我们研究了褪黑激素对病毒诱导的N2a细胞损伤的神经保护作用。 N2a细胞用10μM褪黑素预处理1小时,然后与100μMPrP孵育24小时。褪黑素可显着减轻PrP诱导的N2a细胞凋亡,并抑制PrP诱导的线粒体异常和功能异常,包括线粒体破碎和活性氧(ROS)过量产生,ATP抑制,线粒体膜电位(MMP)降低以及线粒体动态改变蛋白动力蛋白相关蛋白1(DRP1)和视神经萎缩蛋白1(OPA1)。我们的发现表明,褪黑素预处理可预防PrPSc对线粒体功能和动力学的有害影响,保护突触并减轻神经元损伤。褪黑激素可能是治疗病毒疾病的一种新颖有效的药物。

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