Yang Wei Wei, Wang Nan, Zhang Qian Yun, Guan Yu Fei, Wang Si Li, Ma Rui Chen
Department of Anesthesiology, Xi'an No.9 Hospital, Xi'an, Shaanxi, China.
Department of Anesthesiology, Xi'an Da Xing Hospital Affiliated to Yan'an University, Xi'an, Shaanxi, China.
Synapse. 2025 Jul;79(4):e70020. doi: 10.1002/syn.70020.
It has been shown that isoflurane induces persistent neuroinflammation, which can cause morphological and functional changes in brain, leading to cognitive impairment. It is known that miRNAs play an important regulatory role in hippocampal neurodevelopment and plasticity. This study was to investigate the effect of miR-330-5p on isoflurane-induced cognitive deficits in rats and hippocampal neuronal cell lines and to study the underlying mechanisms. Cognitive performance in rats exposed to isoflurane was assessed using the Morris water maze (MWM) test. The levels of inflammation and oxidative stress markers were quantified using enzyme-linked immunosorbent assays (ELISA). Additionally, luciferase reporter assays were employed to validate the interaction between miR-330-5p and its target genes. Isoflurane exposure led to increased miR-330-5p expression in the hippocampal tissues of rats. Suppression of miR-330-5p enhanced cognitive performance, as evidenced by longer durations spent in the target quadrant and reduced escape latencies. Furthermore, isoflurane-induced hippocampal neuronal apoptosis, inflammation, and oxidative stress were alleviated by both a miR-330-5p inhibitor and EPHB3 silencing. Notably, EPHB3 was identified as a direct regulatory target of miR-330-5p. MiR-330-5p exerts neuroprotective effects in rats by regulating EPHB3, which is associated with inflammatory responses, oxidative stress and neuronal apoptosis mediated by the miR-330-5p/EPHB3 axis.
已有研究表明,异氟烷可诱发持续性神经炎症,进而导致大脑的形态和功能发生变化,引发认知障碍。众所周知,微小RNA(miRNAs)在海马体神经发育和可塑性中发挥着重要的调节作用。本研究旨在探讨miR-330-5p对异氟烷诱导的大鼠认知缺陷及海马神经元细胞系的影响,并研究其潜在机制。采用莫里斯水迷宫(MWM)试验评估暴露于异氟烷的大鼠的认知表现。使用酶联免疫吸附测定(ELISA)对炎症和氧化应激标志物的水平进行定量。此外,采用荧光素酶报告基因测定法验证miR-330-5p与其靶基因之间的相互作用。异氟烷暴露导致大鼠海马组织中miR-330-5p表达增加。抑制miR-330-5p可提高认知表现,表现为在目标象限停留的时间更长以及逃避潜伏期缩短。此外,miR-330-5p抑制剂和EPHB3基因沉默均可减轻异氟烷诱导的海马神经元凋亡、炎症和氧化应激。值得注意的是,EPHB3被确定为miR-330-5p的直接调控靶点。miR-330-5p通过调节EPHB3在大鼠中发挥神经保护作用,这与miR-330-5p/EPHB3轴介导的炎症反应、氧化应激和神经元凋亡有关。