异丙酚通过miR-30b调控BecliN-1表达,对肺缺血再灌注损伤具有保护作用。

Huanju Kang, Junjie Chen, Su Cao
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引用次数: 1

摘要

肺缺血再灌注可引起肺泡上皮和肺泡细胞的严重功能障碍。异丙酚等药物对肺缺血再灌注有保护作用,但这种保护机制不稳定,需要核苷等其他因素的参与。本文旨在通过miR-30b调控BecliN-1的表达,研究异丙酚对肺缺血再灌注损伤的保护机制。以72只雄性大鼠为研究对象,建立大鼠肺缺血再灌注模型。采用酚类药物作为灌注液灌注,检测miR-30b和BecliN-1的表达水平,统计实验数据,分析miR-30b对BecliN-1表达的调控机制以及异丙酚对肺缺血-再灌注的保护作用。研究结果表明,异丙酚通过抑制JAK-STAT信号通路的激活,可以减轻炎症、减轻氧化应激、抑制肺组织凋亡、改善肺功能和肺组织病理改变,并且异丙酚可以通过。miR-30b调节BecliN-1表达对肺缺血再灌注损伤的保护作用比其他保护机制高30%。同时,炎性肺组织细胞凋亡率降低13%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Propofol Regulates the Expression of BecliN-1 through miR-30b and Protects against Lung Ischemia-Reperfusion Injury.

Pulmonary ischemia-reperfusion can cause severe dysfunction of alveolar epithelium and alveolar cells. Drugs such as propofol have a protective effect on lung ischemia-reperfusion, but this protective mechanism is not stable and requires other factors such as nucleosides. The purpose of this article is to study the protective mechanism of propofol on lung ischemia-reperfusion injury by regulating the expression of BecliN-1 by miR-30b. With 72 male rats as the research object, a rat lung ischemia-reperfusion model was established. Phenol agents were perfused as the perfusion solution to detect the expression levels of miR-30b and BecliN-1, statistical experimental data and analyze the regulatory mechanism of miR-30b on the expression of BecliN-1 and the effect of propofol on the protection of lung ischemia-reperfusion. Research results show that propofol can reduce inflammation, reduce oxidative stress, inhibit lung tissue apoptosis, improve lung function and pathological changes of lung tissue by inhibiting the activation of the JAK-STAT signaling pathway, and propofol can pass. The protection of miR-30b's regulation of BecliN-1 expression against lung ischemia-reperfusion injury is 30% higher than that of other protective mechanisms. At the same time, the apoptosis rate of inflammatory lung tissue cells is reduced by 13%.

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