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Protective effect of valproic acid on cultured motor neurons under glutamate excitotoxic conditions. Ultrastructural study

机译:谷氨酸兴奋毒性条件下丙戊酸对培养的运动神经元的保护作用。超微结构研究

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摘要

Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder that involves the upper and lower motor neurons and leads to the patient's death within 5 years after diagnosis. Approximately 2 per 100,000 people worldwide are affected every year The only FDA-approved drug available for medical treatment is riluzole. It slows the disease progression and improves limb function and muscle strength for 3-4 months. Thus, looking for new therapeutic agents is a pressing challenge.
机译:肌萎缩性侧索硬化症(ALS)是一种致命的神经退行性疾病,涉及上,下运动神经元,并在诊断后5年内导致患者死亡。每年全球约有每10万人中有2人受到影响。FDA批准的唯一可用于药物治疗的药物是利鲁唑。它可以减慢疾病的进程,并改善肢体功能和肌肉强度,持续3-4个月。因此,寻找新的治疗剂是紧迫的挑战。

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