Yang Eun Jin
KM Medicine Science Research Division, Korea Institute of Oriental Medicine, 1672 Yuseong-Daero, Yuseong-Gu, Daejeon 305811, Republic of Korea.
Evid Based Complement Alternat Med. 2021 Sep 27;2021:6773260. doi: 10.1155/2021/6773260. eCollection 2021.
Amyotrophic lateral sclerosis (ALS) is caused by selective the loss of spinal motor neurons by multifactorial pathological mechanisms and results in muscle atrophy. Incidence rates of ALS are increasing over time, but there are no effective treatments at present due to limitations on approved therapies (riluzole and edaravone). Therefore, this study investigated whether combined treatment with Bojungikgi-tang and riluzole could act synergistically in transactive response DNA-binding protein 43 (TDP-43) stress granule cells. To examine the effect of combined treatment on oxidative stress-induced cell death, the CCK8 assay was performed for the detection of cell viability. The expression of oxidative stress-induced proteins was determined by Western blot. Quantification of sodium arsenite-induced reactive oxygen species (ROS) was measured in TDP-43 stress granular cells using 2,7-diacetyl dichlorofluorescein diacetate. To investigate the effect of combined treatment on TDP-43 aggregation, immunofluorescence and immunoblotting were performed in TDP-43 stress granular cells. This combined treatment alleviated oxidative stress-induced cell death by increasing the expression levels of antioxidation proteins, such as heme oxygenase-1 and B cell lymphoma-2-associated X protein. Furthermore, it reduced oxidative stress-induced TDP-43 aggregates and lowered the levels of autophagy-related proteins, including p62, light chain 3b, and ATG8, in TDP-43-expressing cells. Our results suggest that this combined treatment could be helpful for autophagy regulation in other neurodegenerative diseases.
肌萎缩侧索硬化症(ALS)是由多因素病理机制导致脊髓运动神经元选择性丧失引起的,会导致肌肉萎缩。ALS的发病率随时间增加,但由于批准的治疗方法(利鲁唑和依达拉奉)有限,目前尚无有效的治疗方法。因此,本研究调查了补中益气汤与利鲁唑联合治疗是否能在转录激活反应DNA结合蛋白43(TDP-43)应激颗粒细胞中发挥协同作用。为了检测联合治疗对氧化应激诱导的细胞死亡的影响,进行了CCK8测定以检测细胞活力。通过蛋白质印迹法测定氧化应激诱导蛋白的表达。使用2,7-二乙酰二氯荧光素二乙酸酯在TDP-43应激颗粒细胞中测量亚砷酸钠诱导的活性氧(ROS)的定量。为了研究联合治疗对TDP-43聚集的影响,在TDP-43应激颗粒细胞中进行了免疫荧光和免疫印迹。这种联合治疗通过增加抗氧化蛋白(如血红素加氧酶-1和B细胞淋巴瘤-2相关X蛋白)的表达水平,减轻了氧化应激诱导的细胞死亡。此外,它减少了氧化应激诱导的TDP-43聚集,并降低了TDP-43表达细胞中自噬相关蛋白(包括p62、轻链3b和ATG8)的水平。我们的结果表明,这种联合治疗可能有助于其他神经退行性疾病中的自噬调节。