Department of Psychiatry and Neuroscience, Université Laval, Quebec City G1V 0A6, Canada.
Department of Psychiatry and Neuroscience, Université Laval, Quebec City G1V 0A6, Canada; CERVO Brain Research Centre, Quebec City G1J 2G3, Canada.
Exp Neurol. 2018 Nov;309:193-204. doi: 10.1016/j.expneurol.2018.08.008. Epub 2018 Aug 19.
Withania somnifera (WS; commonly known as Ashwagandha or Indian ginseng) is a medicinal plant whose extracts have been in use for centuries in various regions of the world as a rejuvenator. There is now a growing body of evidence documenting neuroprotective functions of the plant extracts or its purified compounds in several models of neurodegenerative diseases including amyotrophic lateral sclerosis (ALS). Based on the extract's beneficial effect in a mouse model of ALS with TDP-43 proteinopathy, the current study was designed to test its efficacy in another model of familial ALS. Our results show that administration of WS extracts by gavage to mice expressing G93A mutant form of superoxide dismutase (SOD1) resulted in increased longevity, improved motor performance and increased number of motor neurons in lumbar spinal cord. The WS treatment caused substantial reduction in levels of misfolded SOD1whereas it enhanced expression of cellular chaperons in spinal cord of SOD1 mice. WS markedly reduced glial activation and prevented phosphorylation of nuclear factor kappaB (NF-κB). The overall immunomodulatory effect of WS was further evidenced by changes in expression of multiple cytokines/chemokines. WS also served as an autophagy inducer which may be beneficial at early stages of the disease. These results suggest that WS extracts might constitute promising therapeutics for treatment of ALS with involvement of misfolded SOD1.
睡茄(WS;俗称 Ashwagandha 或印度人参)是一种药用植物,其提取物在世界上的许多地区已经使用了几个世纪,作为一种恢复剂。现在有越来越多的证据表明,该植物提取物或其纯化化合物在几种神经退行性疾病模型中具有神经保护功能,包括肌萎缩侧索硬化症(ALS)。基于提取物在 TDP-43 蛋白病的 ALS 小鼠模型中的有益作用,本研究旨在测试其在另一种家族性 ALS 模型中的疗效。我们的结果表明,通过灌胃给予表达超氧化物歧化酶(SOD1)G93A 突变体形式的 WS 提取物可延长寿命、改善运动性能并增加腰椎脊髓中的运动神经元数量。WS 治疗导致错误折叠的 SOD1 水平显著降低,而增强了 SOD1 小鼠脊髓中的细胞伴侣表达。WS 明显减少了神经胶质细胞的激活并阻止了核因子 kappaB(NF-κB)的磷酸化。WS 对多种细胞因子/趋化因子表达的改变进一步证明了其整体免疫调节作用。WS 还作为自噬诱导剂,在疾病的早期阶段可能有益。这些结果表明,WS 提取物可能成为治疗涉及错误折叠 SOD1 的 ALS 的有前途的治疗方法。