氧化应激
脱甲基酶
代谢物
氧化磷酸化
转录因子
化学
谷胱甘肽
KEAP1型
体内
药理学
活性氧
细胞生物学
神经科学
神经毒性
信号转导
兴奋
生物化学
神经保护
神经可塑性
代谢组学
转基因小鼠
毒性
生物
神经退行性变
作者
Lixiao Zhou,Renjie Li,Fu Wang,Ruiqi Zhou,Yinyin Xia,Xuejun Jiang,Shuqun Cheng,Fanghong Wang,Danyang Li,Jun Zhang,Lejiao Mao,Xuemei Cai,Hongyang Zhang,Jingfu Qiu,Xin Tian,Zhen Zou,Chengzhi Chen
标识
DOI:10.1016/j.jhazmat.2024.135736
摘要
Excessive exposure to metals in daily life has been proposed as an environmental risk factor for neurological disorders. Oxidative stress is an inevitable stage involved in the neurotoxic effects induced by metals, nevertheless, the underlying mechanisms are still unclear. In this study, we used arsenic as a representative environmental heavy metal to induce neuronal oxidative stress and demonstrated that both in vitro and in vivo exposure to arsenic significantly increased the level of N6-methyladenosine (m6A) by down-regulating its demethylase FTO. Importantly, the results obtained from FTO transgenic mice and FTO overexpressed/knockout cells indicated that FTO likely regulated neuronal oxidative stress by modulating activating transcription factor 3 (ATF3) in a m
科研通智能强力驱动
Strongly Powered by AbleSci AI