姜黄素抑制 PC12 细胞氧化损伤诱导的神经毒性的策略:ROS 介导的 DNA 损伤及 MAPK 和 AKT 通路的作用。

Strategy to Suppress Oxidative Damage-Induced Neurotoxicity in PC12 Cells by Curcumin: the Role of ROS-Mediated DNA Damage and the MAPK and AKT Pathways.

机构信息

School of Basic Medicine, Taishan Medical University, Taian, 271000, Shandong, China.

Key Lab of Cerebral Microcirculation in Universities of Shandong, Taishan Medical University, Taian, 271000, Shandong, China.

出版信息

Mol Neurobiol. 2016 Jan;53(1):369-378. doi: 10.1007/s12035-014-9021-1. Epub 2014 Nov 30.

Abstract

Oxidative damage plays a key role in causation and progression of neurodegenerative diseases. Inhibition of oxidative stress represents one of the most effective ways in treating human neurologic diseases. Herein, we evaluated the protective effect of curcumin on PC12 cells against H2O2-induced neurotoxicity and investigated its underlying mechanism. The results indicated that curcumin pre-treatment significantly suppressed H2O2-induced cytotoxicity, inhibited the loss of mitochondrial membrane potential (Δψm) through regulation of Bcl-2 family expression, and ultimately reversed H2O2-induced apoptotic cell death in PC12 cells. Attenuation of caspase activation, poly(ADP-ribose) polymerase (PARP) cleavage, DNA damage, and accumulation of reactive oxygen species (ROS) all confirmed its protective effects. Moreover, curcumin markedly alleviated the dysregulation of the MAPK and AKT pathways induced by H2O2. Taken together, our findings suggest that the strategy of using curcumin could be a highly effective way in combating oxidative damage-mediated human neurodegenerative diseases.

摘要

氧化损伤在神经退行性疾病的发生和进展中起着关键作用。抑制氧化应激是治疗人类神经疾病最有效的方法之一。在此,我们评估了姜黄素对 H2O2 诱导的 PC12 细胞神经毒性的保护作用,并探讨了其潜在机制。结果表明,姜黄素预处理可显著抑制 H2O2 诱导的细胞毒性,通过调节 Bcl-2 家族表达抑制线粒体膜电位(Δψm)的丧失,并最终逆转 H2O2 诱导的 PC12 细胞凋亡性细胞死亡。抑制半胱天冬酶激活、多聚(ADP-核糖)聚合酶(PARP)切割、DNA 损伤和活性氧(ROS)的积累都证实了其保护作用。此外,姜黄素显著减轻了 H2O2 诱导的 MAPK 和 AKT 通路的失调。综上所述,我们的研究结果表明,使用姜黄素的策略可能是对抗氧化损伤介导的人类神经退行性疾病的一种非常有效的方法。

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