Zhu Xiaoli
Department of Anesthesiology, Peking University Third Hospital Qinhuangdao Hospital, No. 15, Yufeng Road, West Yanshan Street, Harbor District, Qinhuangdao, Hebei province 066000, China.
Toxicol Res (Camb). 2024 Dec 20;13(6):tfae220. doi: 10.1093/toxres/tfae220. eCollection 2024 Dec.
Sevoflurane (Sev) is a common anesthetic used during surgery, but research on its induction of neurotoxicity and learning memory impairment is insufficient. This study aimed to explore the role of Circular RNA tousled like kinase 1 (circTLK1) and its target microRNA (miR)-374b-5p in Sev-induced neurotoxicity and learning memory impairment.
Mouse hippocampal neuronal HT22 cells and SD rats were treated with Sev. Levels of circTLK1 and miR-374b-5p were detected using RT-qPCR. The concentration of inflammatory factors was determined using ELISA. Cell viability and apoptosis were analyzed using CCK-8 and flow cytometry. Targeting relationship between circTLK1 and miR-374b-5p was validated using dual-luciferase reporter assays and RIP experiments. The Morris water maze test was used to assess the learning and spatial memory abilities of rats.
The results indicated that Sev treatment stimulated neuroinflammation and oxidative stress while increasing circTLK1 levels and decreasing miR-374b-5p levels in both rats and HT22 cells. Silencing circTLK1 alleviated the decrease in cell viability, increased apoptosis rates, and raised concentrations of inflammatory factors caused by Sev treatment. In in vivo experiments, silencing circTLK1 was also found to counteract the oxidative stress, neuroinflammation, and learning and memory impairment induced by Sev treatment in rats. Additionally, circTLK1 was shown to interact with miR-374b-5p, and inhibiting miR-374b-5p could counteract the neuroprotective effects of si-circTLK1.
This research suggested that silencing circTLK1 can mitigate Sev-induced neurotoxicity and learning memory impairment by modulating miR-374b-5p.
七氟醚(Sev)是手术中常用的麻醉剂,但关于其诱导神经毒性和学习记忆障碍的研究尚不充分。本研究旨在探讨环状RNA乱发样激酶1(circTLK1)及其靶向微小RNA(miR)-374b-5p在七氟醚诱导的神经毒性和学习记忆障碍中的作用。
用七氟醚处理小鼠海马神经元HT22细胞和SD大鼠。采用RT-qPCR检测circTLK1和miR-374b-5p的水平。用ELISA法测定炎症因子浓度。采用CCK-8法和流式细胞术分析细胞活力和凋亡情况。通过双荧光素酶报告基因实验和RIP实验验证circTLK1与miR-374b-5p之间的靶向关系。采用Morris水迷宫实验评估大鼠的学习和空间记忆能力。
结果表明,七氟醚处理可刺激神经炎症和氧化应激,并使大鼠和HT22细胞中的circTLK1水平升高,miR-374b-5p水平降低。沉默circTLK1可减轻七氟醚处理导致的细胞活力下降、凋亡率增加以及炎症因子浓度升高。在体内实验中,还发现沉默circTLK1可对抗七氟醚处理诱导的大鼠氧化应激、神经炎症以及学习和记忆障碍。此外,circTLK1可与miR-374b-5p相互作用,抑制miR-374b-5p可抵消si-circTLK1的神经保护作用。
本研究表明,沉默circTLK1可通过调节miR-374b-5p减轻七氟醚诱导的神经毒性和学习记忆障碍。