Department of Anesthesiology, The First Affiliated Hospital of Jinan University, Guangzhou, Guangdong 510632, P.R. China.
Office of Construction, Sun Yat‑Sen University, Guangzhou, Guangdong 510000, P.R. China.
Mol Med Rep. 2023 Apr;27(4). doi: 10.3892/mmr.2023.12970. Epub 2023 Mar 3.
Intubation for general anaesthesia is a life‑threatening risk because it can cause haemodynamic changes. Electroacupuncture (EA) has been reported to alleviate the risk of intubation. In the present study, haemodynamic changes were measured at different time points before and after EA. Reverse transcription‑quantitative PCR was performed to measure the expression of micro (mi)RNAs and endothelial NO synthase (eNOS) mRNA. Western blotting was performed to evaluate the expression of eNOS protein. A luciferase assay was used to explore the inhibitory role of miRNAs in eNOS expression. The transfection of miRNA precursors and antagomirs was performed to assess their effect on eNOS expression. The systolic blood pressure, diastolic blood pressure and mean arterial pressure of patients were significantly decreased by EA, while the heart rate of patients was markedly increased. The expression of micro RNA (miR)‑155, miR‑335 and miR‑383 was effectively inhibited by EA in the plasma and peripheral blood monocytes of patients, whereas eNOS expression and NOS production were markedly elevated by EA. The luciferase activity of the eNOS vector was significantly inhibited by miR‑155, miR‑335 and miR‑383 mimics but activated by miR‑155, miR‑335 and miR‑383 antagomirs. miR‑155, miR‑335 and miR‑383 precursors suppressed the expression of eNOS, while miR‑155, miR‑335 and miR‑383 antagomirs enhanced the expression of eNOS. The present study demonstrated that EA may exert a vasodilative effect during intubation for general anaesthesia by promoting NO production and upregulating eNOS expression. The effect of EA on upregulating eNOS expression may be mediated by its inhibitory effect on the expression of miRNA‑155, miRNA‑335 and miRNA‑383.
全身麻醉下的插管是有生命危险的,因为它会引起血液动力学的变化。电针(EA)已被报道可以降低插管的风险。在本研究中,在 EA 前后的不同时间点测量血液动力学变化。进行逆转录定量 PCR 以测量 microRNA (miRNA) 和内皮型一氧化氮合酶 (eNOS) mRNA 的表达。进行 Western blot 以评估 eNOS 蛋白的表达。进行荧光素酶测定以探索 miRNA 对 eNOS 表达的抑制作用。进行 miRNA 前体和拮抗剂的转染以评估它们对 eNOS 表达的影响。EA 可显著降低患者的收缩压、舒张压和平均动脉压,而显著增加患者的心率。EA 可有效抑制患者血浆和外周血单核细胞中 microRNA (miR)‑155、miR‑335 和 miR‑383 的表达,而 eNOS 表达和 NOS 产生则显著升高。eNOS 载体的荧光素酶活性被 miR‑155、miR‑335 和 miR‑383 模拟物显著抑制,但被 miR‑155、miR‑335 和 miR‑383 拮抗剂激活。miR‑155、miR‑335 和 miR‑383 前体抑制 eNOS 的表达,而 miR‑155、miR‑335 和 miR‑383 拮抗剂增强 eNOS 的表达。本研究表明,EA 通过促进 NO 产生和上调 eNOS 表达,在全身麻醉下插管时可能发挥血管舒张作用。EA 上调 eNOS 表达的作用可能是通过其对 miRNA‑155、miR‑335 和 miRNA‑383 表达的抑制作用介导的。