Cui Yuting, Xiong Yue, Li Hua, Zeng Mengqi, Wang Yan, Li Yuan, Zou Xuan, Lv Weiqiang, Gao Jing, Cao Ruijun, Meng Lingjie, Long Jiangang, Liu Jiankang, Feng Zhihui
Center for Mitochondrial Biology and Medicine, The Key Laboratory of Biomedical Information Engineering of Ministry of Education, School of Life Science and Technology, Xi'an Jiaotong University, Xi'an 710049, China.
Institute of Basic Medical Science, Xi'an Medical University, Xi'an 710021, China.
Antioxidants (Basel). 2021 Nov 15;10(11):1811. doi: 10.3390/antiox10111811.
NF-E2-related factor 2 (Nrf2), the key transcription regulator of phase II enzymes, has been considered beneficial for neuronal protection. We previously designed a novel chalcone analog, 1-(2,3,4-trimethoxyphenyl)-2-(3,4,5-trimethoxyphenyl)-acrylketone (Tak), that could specifically activate Nrf2 in vitro. Here, we report that Tak confers significant hippocampal neuronal protection both in vitro and in vivo. Treatment with Tak has no significant toxicity on cultured neuronal cells. Instead, Tak increases cellular ATP production by increasing mitochondrial function and decreases the levels of reactive oxygen species by activating Nrf2-mediated phase II enzyme expression. Tak pretreatment prevents glutamate-induced excitotoxic neuronal death accompanied by suppressed mitochondrial respiration, increased superoxide production, and activation of apoptosis. Further investigation indicates that the protective effect of Tak is mediated by the Akt signaling pathway. Meanwhile, Tak administration in mice can sufficiently abrogate scopolamine-induced cognitive impairment via decreasing hippocampal oxidative stress. In addition, consistent benefits are also observed in an energy stress mouse model under a high-fat diet, as the administration of Tak remarkably increases Akt signaling-mediated antioxidative enzyme expression and prevents hippocampal neuronal apoptosis without significant effect on the mouse metabolic status. Overall, our study demonstrates that Tak protects cognitive function by Akt-mediated Nrf2 activation to maintain redox status both vivo and in vitro, suggesting that Tak is a promising pharmacological candidate for the treatment of oxidative neuronal diseases.
核因子E2相关因子2(Nrf2)是II期酶的关键转录调节因子,被认为对神经元保护有益。我们之前设计了一种新型查尔酮类似物,1-(2,3,4-三甲氧基苯基)-2-(3,4,5-三甲氧基苯基)-丙烯酮(Tak),它在体外能特异性激活Nrf2。在此,我们报告Tak在体外和体内均能赋予显著的海马神经元保护作用。Tak处理对培养的神经元细胞无明显毒性。相反,Tak通过增强线粒体功能增加细胞ATP生成,并通过激活Nrf2介导的II期酶表达降低活性氧水平。Tak预处理可预防谷氨酸诱导的兴奋性毒性神经元死亡,同时伴有线粒体呼吸抑制、超氧化物生成增加和凋亡激活。进一步研究表明,Tak的保护作用是由Akt信号通路介导的。同时,给小鼠施用Tak可通过减轻海马氧化应激充分消除东莨菪碱诱导的认知障碍。此外,在高脂饮食的能量应激小鼠模型中也观察到了一致的益处,因为施用Tak可显著增加Akt信号介导的抗氧化酶表达并预防海马神经元凋亡,而对小鼠代谢状态无显著影响。总体而言,我们的研究表明,Tak通过Akt介导的Nrf2激活保护认知功能,以在体内和体外维持氧化还原状态,提示Tak是治疗氧化性神经元疾病的一种有前景的药理学候选物。