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miR-188-3p 通过靶向 MDM2 参与七氟醚麻醉诱导的神经细胞凋亡。

MicroRNA-188-3p is involved in sevoflurane anesthesia-induced neuroapoptosis by targeting MDM2.

机构信息

Department of Anesthesia, Cangzhou Central Hospital, Cangzhou, Hebei 061001, P.R. China.

出版信息

Mol Med Rep. 2018 Mar;17(3):4229-4236. doi: 10.3892/mmr.2018.8437. Epub 2018 Jan 16.

Abstract

Sevoflurane is a commonly used inhalation anesthetic. Sevoflurane-induced neuroapoptosis and cognitive impairments in animals are widely reported, however, the underlying molecular mechanisms remain largely unknown. The results of the present study demonstrated that sevoflurane anesthesia induced spatial memory impairments in rats, as determined by the Morris water maze test. Mechanistically, the current study demonstrated that sevoflurane administration significantly enhanced the expression of microRNA (miR)‑188‑3p. Furthermore, inhibition of miR‑188‑3p using lentiviral miR‑188‑3p inhibitors attenuated sevoflurane‑induced cognitive impairments in rats. The present study also demonstrated that miR‑188‑3p targeted MDM2 proto‑oncogene (MDM2) and negatively regulated the expression of MDM2, as determined by luciferase assays, reverse transcription‑quantitative polymerase chain reaction and western blot analysis. Furthermore, decreased abundance of MDM2 following transfection with miR‑188‑3p mimics was associated with increased stability of p53 protein. Suppression of p53 activity using the specific p53 inhibitor pifithrin‑α alleviated sevoflurane‑induced neuroapoptosis. These results indicate that the miR‑188‑3p‑MDM2‑p53 axis may have a critical role in sevoflurane‑induced cognitive dysfunction. Therefore, miR‑188‑3p may be a potential target for the treatment of sevoflurane‑induced cognitive impairment.

摘要

七氟醚是一种常用的吸入麻醉剂。广泛报道了七氟醚诱导的动物神经细胞凋亡和认知功能障碍,但潜在的分子机制在很大程度上尚不清楚。本研究结果表明,七氟醚麻醉通过 Morris 水迷宫试验诱导大鼠空间记忆损伤。从机制上讲,本研究表明,七氟醚给药显著增强了 microRNA(miR)-188-3p 的表达。此外,使用慢病毒 miR-188-3p 抑制剂抑制 miR-188-3p 可减轻大鼠七氟醚诱导的认知障碍。本研究还表明,miR-188-3p 靶向 MDM2 原癌基因(MDM2),并通过荧光素酶测定、逆转录-定量聚合酶链反应和 Western blot 分析负调控 MDM2 的表达。此外,转染 miR-188-3p 模拟物后 MDM2 的丰度降低与 p53 蛋白稳定性增加有关。使用特异性 p53 抑制剂 pifithrin-α 抑制 p53 活性可减轻七氟醚诱导的神经细胞凋亡。这些结果表明,miR-188-3p-MDM2-p53 轴在七氟醚诱导的认知功能障碍中可能具有重要作用。因此,miR-188-3p 可能是治疗七氟醚诱导的认知障碍的潜在靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b233/5802194/ae62c0a64f5a/MMR-17-03-4229-g00.jpg

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