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提取物通过激活氧化还原体-p66Shc保护人神经母细胞瘤SH-SY5Y细胞免受氧化型谷氨酸毒性的影响。

extract protects human neuroblastoma SH-SY5Y cells against oxidative glutamate toxicity by activating redoxosome-p66Shc.

作者信息

Wang Ke, Ni Jing, Zhu Xue, Zhu Ling, Li Yue, Zhou Fanfan

机构信息

NHC Key Laboratory of Nuclear Medicine, Jiangsu Key Laboratory of Molecular Nuclear Medicine, Jiangsu Institute of Nuclear Medicine, Wuxi, Jiangsu 214063, P.R. China.

Department of Geriatric Rehabilitation, Jiangsu Rongjun Hospital, Wuxi, Jiangsu 214035, P.R. China.

出版信息

Exp Ther Med. 2021 Sep;22(3):951. doi: 10.3892/etm.2021.10383. Epub 2021 Jul 5.

Abstract

extract (GBE), a traditional Chinese herbal medicine component, is widely used to alleviate symptoms of neurodegenerative diseases. It has been confirmed that GBE exerts its pharmacological effect mainly due to its antioxidant activity; however, the molecular mechanism responsible for this effect remains unclear. The aim of the present study was to investigate the detailed mechanism of GBE, the main component of dropping medicine, against oxidative glutamate toxicity in human neuroblastoma SH-SY5Y cells. The SH-SY5Y cells were untreated or pretreated with GBE followed by glutamate stimulation. Cell viability was assessed using an MTT assay. In addition, oxidative stress indexes, including intracellular ROS generation and NADPH oxidase and caspase activity, were also measured. The protein expression of key signaling factors involved in the redoxosome-p66Shc pathway was evaluated to elucidate the neuroprotective effect of GBE. The results showed that GBE treatment significantly attenuated the glutamate-induced cytotoxicity in SH-SY5Y cells by suppressing oxidative stress. A mechanical study revealed that redoxosome-p66Shc activation was associated with glutamate-induced cytotoxicity, which caused mitochondrial dysfunction and cell death. Interestingly, GBE treatment attenuated the activation of redoxosome-p66Shc in a dose-dependent manner, which suggested that the protective effect of GBE on SH-SY5Y cells against oxidative glutamate toxicity may be mediated by the modulation of redoxosome-p66Shc signaling. The current findings contribute to a better understanding of the therapeutic effect of GBE and indicate that redoxosome-p66Shc signaling might be a novel therapeutic target in the prevention and/or treatment of neurodegenerative diseases.

摘要

银杏叶提取物(GBE)是一种传统的中草药成分,被广泛用于缓解神经退行性疾病的症状。已经证实,GBE发挥其药理作用主要是由于其抗氧化活性;然而,负责这种作用的分子机制仍不清楚。本研究的目的是探讨滴丸剂的主要成分GBE对人神经母细胞瘤SH-SY5Y细胞氧化谷氨酸毒性的详细作用机制。SH-SY5Y细胞未处理或用GBE预处理,然后进行谷氨酸刺激。使用MTT法评估细胞活力。此外,还测量了氧化应激指标,包括细胞内活性氧生成、NADPH氧化酶和半胱天冬酶活性。评估了参与氧化还原体-p66Shc途径的关键信号因子的蛋白表达,以阐明GBE的神经保护作用。结果表明,GBE处理通过抑制氧化应激显著减轻了谷氨酸诱导的SH-SY5Y细胞毒性。一项机制研究表明,氧化还原体-p66Shc激活与谷氨酸诱导的细胞毒性有关,后者导致线粒体功能障碍和细胞死亡。有趣的是,GBE处理以剂量依赖的方式减弱了氧化还原体-p66Shc的激活,这表明GBE对SH-SY5Y细胞抗氧化谷氨酸毒性的保护作用可能是通过调节氧化还原体-p66Shc信号介导的。目前的研究结果有助于更好地理解GBE的治疗效果,并表明氧化还原体-p66Shc信号可能是预防和/或治疗神经退行性疾病的一个新的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5cce/8290427/1d4855ab6d71/etm-22-03-10383-g00.jpg

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