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首页> 外文期刊>藥學雜誌 >伝統薬物による神経変性疾患の克服 治療薬開発と病態機序の解明に向けて
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伝統薬物による神経変性疾患の克服 治療薬開発と病態機序の解明に向けて

机译:用传统药物克服神经退行性疾病走向治疗药物的发展及其病理机制的阐明

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Ashwagandha (root of Withania somnifera) has been used for many purposes, it is mainly considered a tonic in traditional Ayurvedic medicine. This review focuses on the effects of compounds isolated from Ashwagandha on dementia models and on the spinal cord injury model. Our study demonstrated that the active constituents, withanolide A, withanoside IV, and withanoside VI, restored presynapses and postsynapses, in addition to both axons and dendrites in cortical neurons after Abeta(25-35) -induced injury. In vivo, oral withanolide A, withanoside IV, and withanoside VI (10 mumol/kg/day for 12 days) improved Abeta (25-35) -induced memory impairment, neurite atrophy, and synaptic loss in the cerebral cortex and hippocampus in mice. Since spinal cord injury (SCI) is also difficult to treat, and therefore practical and curable strategies for SCI are desired. Oral treatment with withanoside IV improved locomotor functions in mice with SCI. In mice treated with withanoside IV (10 mumol/kg/day for 21 days), the axonal density and peripheral nervous system myelin level increased. The loss of CNS myelin and increase in reactive gliosis were not affected by withanoside IV. Additionally, sominone, an aglycone of withanoside IV, was identified as the main metabolite after oral administration of withanoside IV in mice. Withanolide A, withanoside IV, and withanoside VI are therefore important candidates for the therapeutic treatment of neurodegenerative diseases. In particular, withanoside IV was shown to control neurons as well as glial cells for reconstruction neuronal networks. To clarify key events in overcoming neurodegeneration, we are now studying the molecular targets and signal cascades of sominone.
机译:Ashwagandha(Withania somnifera的根)已被用于许多目的,它在传统的印度草药中被认为是补品。这篇综述着重于从非洲醉茄中分离出的化合物对痴呆模型和脊髓损伤模型的影响。我们的研究表明,Abeta(25-35)诱导的损伤后,除了皮质神经元中的轴突和树突外,活性成分withanolide A,withanoside IV和withanoside VI还恢复了突触前和突触后。在体内,口服withanolide A,withanoside IV和withanoside VI(10摩尔/千克/天,共12天)改善了Abeta(25-35)诱导的小鼠大脑皮质和海马体的记忆力受损,神经突萎缩和突触丧失。由于脊髓损伤(SCI)也难以治疗,因此需要实用且可治愈的SCI策略。用山梨糖苷IV口服治疗可改善SCI小鼠的运动功能。在用anosideside IV(10摩尔/千克/天,共21天)治疗的小鼠中,轴突密度和周围神经系统髓磷脂水平升高。苦参皂甙IV不会影响CNS髓磷脂的丢失和反应性神经胶质增生。另外,在小鼠中口服withanoside IV后,紫苏甙,withanoside IV的糖苷配基被鉴定为主要代谢产物。因此,Withanolide A,withanoside IV和withanoside VI是治疗神经退行性疾病的重要候选药物。特别是,withanoside IV已显示可控制神经元以及用于重建神经元网络的神经胶质细胞。为了阐明克服神经变性的关键事件,我们现在正在研究氨酮的分子靶标和信号级联。

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