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SC79可保护多巴胺能神经元免受氧化应激损伤。

SC79 protects dopaminergic neurons from oxidative stress.

作者信息

Xu Yan, Gao Ya-Wen, Yang Yu

机构信息

Geriatrics Department, The Second Xiang Ya Hospital of Central South University, Changsha, China.

出版信息

Oncotarget. 2017 Dec 20;9(16):12639-12648. doi: 10.18632/oncotarget.23538. eCollection 2018 Feb 27.

Abstract

Oxidative stress could lead to dopaminergic neuronal cell death. SC79 is a novel, selective and highly-efficient Akt activator. The current study tested its effect in dopaminergic neurons with oxidative stress. In both SH-SY5Y cells and primary murine dopaminergic neurons, pre-treatment with SC79 largely inhibited hydrogen peroxide (HO)-induced cell viability reduction, apoptosis and necrosis. SC79 activated Akt in the neuronal cells, which was required for its neuroprotection against HO. Inhibition of Akt activation (by MK-2206 or AT7867) or expression (by targeted short hairpin RNA) largely attenuated SC79-induced neuroprotection. Further, CRISPR-Cas9-mediated Akt1 knockout in SH-SY5Y cells abolished SC79-induced neuroprotective function against H2O2. Reversely, forced activation of Akt by the constitutively-active Akt1 mimicked SC79-induced anti-HO activity. Together, we conclude that activation of Akt by SC79 protects dopaminergic neurons from HO.

摘要

氧化应激可导致多巴胺能神经元细胞死亡。SC79是一种新型、选择性且高效的Akt激活剂。本研究测试了其在氧化应激的多巴胺能神经元中的作用。在SH-SY5Y细胞和原代小鼠多巴胺能神经元中,用SC79预处理可显著抑制过氧化氢(H₂O₂)诱导的细胞活力降低、凋亡和坏死。SC79在神经元细胞中激活Akt,这是其对H₂O₂发挥神经保护作用所必需的。抑制Akt激活(通过MK-2206或AT7867)或表达(通过靶向短发夹RNA)可大大减弱SC79诱导的神经保护作用。此外,CRISPR-Cas9介导的SH-SY5Y细胞中Akt1基因敲除消除了SC79诱导的对H₂O₂的神经保护功能。相反,组成型活性Akt1强制激活Akt可模拟SC79诱导的抗H₂O₂活性。总之,我们得出结论,SC79激活Akt可保护多巴胺能神经元免受H₂O₂损伤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3430/5849161/58ac2c4aa598/oncotarget-09-12639-g001.jpg

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