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三七皂苷R1通过抑制活性氧和调节丝裂原活化蛋白激酶(MAPK)的激活来减轻淀粉样β蛋白诱导的神经元损伤。

Notoginsenoside R1 attenuates amyloid-β-induced damage in neurons by inhibiting reactive oxygen species and modulating MAPK activation.

作者信息

Ma Bo, Meng Xiangbao, Wang Jing, Sun Jing, Ren Xiaoyu, Qin Meng, Sun Jie, Sun Guibo, Sun Xiaobo

机构信息

Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences and Peking Union Medical College, 151, Malianwa North Road, Haidian District, Beijing 100193, PR China.

Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences and Peking Union Medical College, 151, Malianwa North Road, Haidian District, Beijing 100193, PR China; Eastern Liaoning University, No. 325 Wenhua Street, Yuanbao District, Dandong Liaoning 118003, PR China.

出版信息

Int Immunopharmacol. 2014 Sep;22(1):151-9. doi: 10.1016/j.intimp.2014.06.018. Epub 2014 Jun 24.

Abstract

Progressive accumulation of amyloid-β (Aβ) is a pathological hallmark of Alzheimer's disease (AD). Aβ increases free radical production in neuronal cells, leading to oxidative stress and cell death. An intervention that would reduce Aβ-related neurotoxicity through free radical reduction could advance the treatment of AD. Notoginsenoside R1 (NR1), the major and most active ingredient in the herb Panax notoginseng, can reduce reactive oxygen species and confer some neuroprotective effects. Here, NR1 was applied in a cell-based model of Alzheimer's disease. Cell viability, cell death, reactive oxygen species generation, and mitochondrial membrane potential were assessed in cultured PC12 neuronal cells incubated with Aβ(25-35). In this model, Aβ was neurotoxic and induced necrosis and apoptosis; however, NR1 significantly counteracted the effects of Aβ by increasing cell viability, reducing oxidative damage (including apoptosis), restoring mitochondrial membrane potential, and suppressing stress-activated MAPK signaling pathways. These results promise a great potential agent for Alzheimer's disease and other Aβ pathology-related neuronal degenerative disease.

摘要

β-淀粉样蛋白(Aβ)的渐进性积累是阿尔茨海默病(AD)的病理标志。Aβ会增加神经元细胞中的自由基产生,导致氧化应激和细胞死亡。一种通过减少自由基来降低Aβ相关神经毒性的干预措施可能会推动AD的治疗。三七皂苷R1(NR1)是草药三七中的主要且最具活性的成分,它可以减少活性氧并具有一定的神经保护作用。在此,NR1被应用于阿尔茨海默病的细胞模型中。在用Aβ(25-35)孵育的培养PC12神经元细胞中评估细胞活力、细胞死亡、活性氧产生和线粒体膜电位。在该模型中,Aβ具有神经毒性并诱导坏死和凋亡;然而,NR1通过提高细胞活力、减少氧化损伤(包括凋亡)、恢复线粒体膜电位以及抑制应激激活的MAPK信号通路,显著抵消了Aβ的作用。这些结果表明NR1有望成为治疗阿尔茨海默病和其他与Aβ病理相关的神经元退行性疾病的极具潜力的药物。

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