Zhou Chuanlin, Lian Fang, Li Hejian, Deng Fumou
Queen Mary School, Nanchang University, Nanchang, 330006 Jiangxi China.
Department of Anesthesiology, the Second Affiliated Hospital of Nanchang University, Nanchang, 330006 Jiangxi China.
3 Biotech. 2025 Jan;15(1):16. doi: 10.1007/s13205-024-04176-3. Epub 2024 Dec 18.
The aim of this research is to investigate whether ferroptosis occurs in the pathogenesis of perioperative neurocognitive disorders (PND), and to explore the function and underlying molecular mechanism of tsRNA in the regulation of ferroptosis in PND. A PND aged mice model was established and behavioral changes and ferroptosis occurrence were confirmed. The effect of ferroptosis inhibitor ferrostatin-1 (Fer-1) on PND mice was detected. tsRNA expression profile in PND mice and the effect of tsRNA on ferroptosis in vitro were perfomed. We found that anxious exploration behavior and short-term working memory was declined in PND mice compared with control mice, and the levels of S100β and IL-6 were increased. Meanwhile, hippocampal neurons of PND mice were damaged and accompanied by ferroptosis. Fer-1 can improve cognitive impairment in PND mice, as reflected by improved anxious exploration behavior and short-term working memory, and the levels of S100β and IL-6 were decreased. The expression profile of tsRNA in PND mice is disordered, and the dysregulated tsRNAs were mainly enriched in biologic functions related to neuronal development and ferroptosis. The tsRNA-5006c, identified as a pivotal player, significantly suppressed ferroptosis in primary mice neurons. This study shows for the first time that the pathophysiological process of PND is accompanied by ferroptosis of neurons, and reveals that tsRNA-5006c regulates ferroptosis of hippocampal neurons to ameliorate PND, which is of great significance for the development of new treatment strategies.
The online version contains supplementary material available at 10.1007/s13205-024-04176-3.
本研究旨在探讨铁死亡是否发生在围手术期神经认知障碍(PND)的发病机制中,并探索tsRNA在PND中铁死亡调控的作用及潜在分子机制。建立了PND老年小鼠模型,并证实了行为变化和铁死亡的发生。检测了铁死亡抑制剂铁抑素-1(Fer-1)对PND小鼠的影响。分析了PND小鼠的tsRNA表达谱以及tsRNA在体外对铁死亡的影响。我们发现,与对照小鼠相比,PND小鼠的焦虑探索行为和短期工作记忆下降,S100β和IL-6水平升高。同时,PND小鼠的海马神经元受损并伴有铁死亡。Fer-1可以改善PND小鼠的认知障碍,表现为焦虑探索行为和短期工作记忆得到改善,S100β和IL-6水平降低。PND小鼠中tsRNA的表达谱紊乱,失调的tsRNAs主要富集在与神经元发育和铁死亡相关的生物学功能中。被确定为关键因子的tsRNA-5006c显著抑制原代小鼠神经元中的铁死亡。本研究首次表明,PND的病理生理过程伴有神经元铁死亡,并揭示tsRNA-5006c调节海马神经元铁死亡以改善PND,这对新治疗策略的开发具有重要意义。
在线版本包含可在10.1007/s13205-024-04176-3获取的补充材料。