Jingyan Cheng, Guoyuan Pan, Zhen Wang, Haoran Chu, Yanpeng Pu
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引用次数: 0
摘要
背景介绍电针(EA)是一种传统的中医物理疗法,已广泛应用于临床。本文旨在探讨电针治疗对大脑中动脉闭塞(MCAO)小鼠突触可塑性的影响,并阐明相关的分子机制:方法:MCAO建模后,C57BL/6小鼠接受EA治疗或/和miR-670-3p模拟物注射,然后用改良神经严重程度评分(mNSS)评估神经功能缺损情况,并用TTC染色评估脑梗死面积。利用透射电子显微镜(TEM)观察突触超微结构相关参数的变化。通过 RT-qPCR 和 Western 印迹分析量化了 miR-670-3p、HMGB1、TLR4/NF-κB 通路相关蛋白和突触相关蛋白(突触素 1、PSD95、BDNF 和 GAP43)的表达水平。通过双荧光素酶报告实验和 RNA pull down 实验评估了 miR-670-3p 与 HMGB1 之间的结合关系:结果:接受 EA 治疗或注射 miR-670-3p 模拟物的小鼠表现出 miR-670-3p 表达增加、HMGB1 和 TLR4/NF-κB 通路相关蛋白表达水平降低、神经功能改善和突触可塑性增强。此外,EA治疗和miR-670-3p模拟物注射相结合产生了协同效应,进一步扩大了这些结果。从机理上讲,miR-670-3p 能负向调节 HMGB1:EA治疗通过促进miR-670-3p的表达来负向调节HMGB1/TLR4/NF-κB通路,从而增强MCAO小鼠的突触可塑性。
Electroacupuncture treatment enhances synaptic plasticity in middle cerebral artery occlusion mice via the miR-670-3p/HMGB1 axis.
Background: Electroacupuncture (EA) is a physical therapy of traditional Chinese medicine, which has been widely used in clinical practice. This paper was designed to explore the effect of EA treatment on synaptic plasticity in mice subjected to middle cerebral artery occlusion (MCAO) and to elucidate the associated molecular mechanisms.
Methods: After MCAO modeling, C57BL/6 mice underwent EA treatment or/and miR-670-3p mimic injection, followed by assessment of neurological deficit by modified neurological severity score (mNSS) and evaluation on cerebral infarction area by TTC staining. The changes of synaptic ultrastructure related parameters were observed using transmission electron microscopy (TEM). The expression levels of miR-670-3p, HMGB1, TLR4/NF-κB pathway related proteins, and synaptic associated proteins (synapsin 1, PSD95, BDNF, and GAP43) were quantified by RT-qPCR and western blot analysis. The binding relationship between miR-670-3p and HMGB1 was assessed through dual-luciferase reporter assays and RNA pull down assays.
Results: Mice underwent EA treatment or miR-670-3p mimic injection exhibited increased miR-670-3p expression, reduced expression levels of HMGB1 and TLR4/NF-κB pathway related proteins, improved neurological function, and enhanced synaptic plasticity. Furthermore, the combination of EA treatment and miR-670-3p mimic injection produced a synergistic effect, further amplifying these outcomes. Mechanistically, miR-670-3p was found to negatively regulate HMGB1.
Conclusion: EA treatment enhances synaptic plasticity in MCAO mice by promoting miR-670-3p expression to negatively regulate the HMGB1/TLR4/NF-κB pathway.