Department of Anesthesia, Cancer Hospital of China Medical University, Liaoning Cancer Hospital & Institute, Shenyang, Liaoning, China.
J Invest Surg. 2021 Nov;34(11):1167-1177. doi: 10.1080/08941939.2020.1771639. Epub 2020 Jun 7.
To investigate effects of circular RNA (circRNA) 001372 and its antagonist miRNAs-148b-3p on propofol-induced neurotoxicity and neuroinflammation in rat brain and pheochromocytoma cells.
Sprague Dawley rats in propofol model group (n = 6) were intraperitoneal injected with propofol (50 mg/kg) and in sham control group (n = 6) without any treatment. Twenty-four h later, brain tissues were acquired during pentobarbital anesthesia. PC-12 cells were transfected with or without circRNA001372 mimics, circRNA001372 inhibitor, negative mimics or miRNA-148b-3p for 48 h and then treated with propofol (100 μM) for 48 h. Quantitative reverse transcription PCR and gene chips were used for detecting levels of circRNA001372, Haemotoxylin and Eosin staining for cell morphology, MTT for cell viability, flow cytometry for apoptosis, enzyme-linked immunosorbent assay for lactate dehydrogenase (LDH), interleukin-1β (IL-1β), IL-6, IL17 and IL-18, and Western blots for phosphoinositide 3-kinase (PI3K), Akt, phosphorylated Akt, and nuclear factor (NF) κB, dual-light luminescent reporter gene assay for luciferase reporter.
The propofol anesthesia in rats decreases levels of circRNA001372 and increases levels of cytokines including IL-1β, IL-6, IL17 and IL-18, resulting in the neurocyte damage in brain. In propofol-treated PC-12 cells, the inhibition of circRNA001372 increases apoptosis and cell damage makers, including LDH, IL-1β, IL-6, IL17, IL-18, resulting in the reduction of cell viability, which have been revised after over-expression of circRNA001372. MiRNA-148b-3p reduces circRNA001372-incresed PI3K and pAKt levels but enhances the circRNA001372-decreased NFκB level.
CircRNA001372 suppresses propofol-induced neurotoxicity and neuroinflammation through PI3K/Akt/NF-κB signaling pathway in rat brain and neurocytes. MiRNA-148b-3p antagonizes the effects of circRNA001372.
研究环状 RNA(circRNA)001372及其拮抗剂 miRNA-148b-3p 对大鼠脑和嗜铬细胞瘤细胞中异丙酚诱导的神经毒性和神经炎症的影响。
在异丙酚模型组(n=6)大鼠腹腔注射异丙酚(50mg/kg),在假手术对照组(n=6)大鼠不做任何处理。24 h 后,在戊巴比妥麻醉下获取脑组织。PC-12 细胞转染或不转染 circRNA001372 模拟物、circRNA001372 抑制剂、阴性模拟物或 miRNA-148b-3p,转染 48 h 后用 100 μM 异丙酚处理 48 h。采用定量逆转录 PCR 和基因芯片检测 circRNA001372 水平,苏木精和伊红染色观察细胞形态,MTT 法检测细胞活力,流式细胞术检测细胞凋亡,酶联免疫吸附试验检测乳酸脱氢酶(LDH)、白细胞介素-1β(IL-1β)、白细胞介素-6(IL-6)、白细胞介素-17(IL-17)和白细胞介素-18(IL-18)水平,Western blot 检测磷酸肌醇 3-激酶(PI3K)、Akt、磷酸化 Akt 和核因子(NF)κB 水平,双荧光素酶报告基因检测试剂盒检测荧光素酶报告。
异丙酚麻醉降低了大鼠脑中 circRNA001372 的水平,并增加了包括 IL-1β、IL-6、IL17 和 IL-18 在内的细胞因子水平,导致脑神经元损伤。在异丙酚处理的 PC-12 细胞中,circRNA001372 的抑制增加了细胞损伤标志物,包括 LDH、IL-1β、IL-6、IL17、IL-18,导致细胞活力降低,而过表达 circRNA001372 后这些指标得到了修正。miRNA-148b-3p 降低了 circRNA001372 增加的 PI3K 和 pAKt 水平,但增强了 circRNA001372 降低的 NFκB 水平。
circRNA001372 通过大鼠脑和神经细胞中的 PI3K/Akt/NF-κB 信号通路抑制异丙酚诱导的神经毒性和神经炎症。miRNA-148b-3p 拮抗 circRNA001372 的作用。