川芎嗪通过调节miR-211/USP47通路增强瑞芬太尼对心肌缺血再灌注损伤的保护作用

Xin Li, D. Xia
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引用次数: 0

摘要

目的:评价川芎嗪对心肌缺血再灌注(I/R)损伤进展的影响,探讨miR-211在心肌缺血再灌注(I/R)损伤中的可能作用,并鉴定其潜在靶向基因。方法:采用定量聚合酶链反应法检测H/ r诱导细胞中miR-211的表达水平。通过CCK-8、流式细胞术(FCM)和Western blot检测miR-211和USP47对瑞芬太尼抗H/R损伤作用的影响。通过生物信息学分析、荧光素酶和Western blot检测来鉴定和验证miR-211的潜在靶点。CCK-8和FCM检测川芎嗪和miR-211对瑞芬太尼抗H/ r诱导细胞的保护作用机制。结果:川芎嗪增强了瑞芬太尼对H/ r诱导心肌细胞的影响。MiR-211增强了瑞芬太尼对H/R损伤的保护作用。下调USP47可增强瑞芬太尼对H/R损伤的保护作用。川芎嗪通过miR-211/USP47通路增强瑞芬太尼对H/R损伤的保护作用。结论:川芎嗪通过调节miR-211/USP47通路增强瑞芬太尼对心肌I/R损伤的保护作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ligustrazine enhances the protective effect of remifentanil on myocardial ischemia-reperfusion injury by regulating miR-211/USP47 pathway
Purpose: To assess the effects of ligustrazine on the progression of hypoxia-reoxygenation (H/R), and explore the possible role of miR-211 in myocardial ischemia-reperfusion (I/R) injury and identify its potential targeting gene. Methods: The level of miR-211 in H/R-induced cells was detected by quantitative polymerase chain reaction. CCK-8, flow cytometry (FCM), and Western blot assays were performed to examine the effect of miR-211 and USP47 on the role of remifentanil against H/R injury. Bioinformatic analysis and luciferase and Western blot assays were performed to identify and verify the potential target of miR-211. CCK-8 and FCM assays were performed to detect the mechanism of ligustrazine and miR-211 in the protection of remifentanil against H/R-induced cells. Results: Ligustrazine enhanced the effect of remifentanil on H/R-induced cardiomyocytes. MiR-211 enhanced the protective effect of remifentanil against H/R injury. Down-regulation of USP47 enhanced the protective effect of remifentanil against H/R injury. Ligustrazine enhanced the protective effect of remifentanil against H/R injury through miR-211/USP47 pathway. Conclusion: Ligustrazine enhanced the protective effect of remifentanil on myocardial I/R injury by regulating miR-211/USP47 pathway.
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