针灸调节 AMPK/PGC-1 信号通路,促进缺血性中风大鼠线粒体生物生成和神经恢复

Kaixin Guo, Yan Lu
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摘要

本研究的主要目的是探讨针灸通过单磷酸激活蛋白激酶(AMPK)/过氧化物酶体增殖物激活受体-γ辅助激活因子1α(PGC-1α)轴调节线粒体能量代谢,在大鼠缺血性中风急性期抗神经损伤的作用和机制。在缺血性脑卒中急性期进行为期一周的针刺治疗。对神经功能和脑组织完整性进行了评估。通过酶化学方法检测了线粒体功能(细胞内 ATP 水平和线粒体呼吸链复合物 I 的活性)和 NADH 氧化酶(NOX)水平。结果表明:(1) 针刺治疗MCAO/R大鼠后,梗死组织明显改善,Zea-Longa评分、平衡木评分、运动功能恢复。(2)针刺提高了缝合闭塞法脑缺血大鼠的 ATP 和线粒体呼吸链复合物 I 的水平,降低了 NOX 的水平。(3)针刺减少了神经细胞的坏死溶解和脑膜水肿,同时促进了血管生成。(4)免疫组化定量染色结果显示,针刺能增加AMPK、p-AMPK和线粒体转录因子PGC-1α、NRF2、TFAM和解偶联蛋白2(UCP2)的表达。同时,针灸治疗可上调相应蛋白的表达。(5) 随后,针灸增强了 AMPK 磷酸化以及与线粒体合成和细胞凋亡有关的 PGC-1α、NRF2、TFAM 和 UCP2 的表达。(针灸干预通过促进脑内能量代谢和线粒体的生物生成,缓解MCAO大鼠缺血性中风的进展,而这是通过激发AMPK/PGC-1α轴来实现的,其中AMPK是一个治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Acupuncture modulates the AMPK/PGC-1 signaling pathway to facilitate mitochondrial biogenesis and neural recovery in ischemic stroke rats
The main objective of this study was to investigate the role and mechanism of acupuncture on anti-nerve injury in the acute phase by regulating mitochondrial energy metabolism via monophosphate-activated protein kinase (AMPK)/peroxisome proliferator-activated receptor-γ coactivator 1α (PGC-1α) axis in rat ischemic stroke.Middle cerebral artery occlusion (MCAO) was established by middle cerebral artery occlusion/reperfusion. One-week of acupuncture was performed during the acute phase of ischemic stroke. The neurological function and brain tissue integrity were evaluated. Mitochondrial function (intracellular ATP level and the activity of mitochondrial respiratory chain complex I) and the level of NADH oxidase (NOX) were detected by enzymatic chemistry. Next, the potential molecular mechanisms were explored by western blotting, fluorescence quantitative PCR and immunohistochemistry method.(1) Acupuncture treatment for MCAO/R rats showed a significant improvement in the infarcted tissue accompanied by functional recovery in Zea-Longa score and balance beam score outcomes, motor function performances. (2) Acupuncture increased the levels of ATP and mitochondrial respiratory chain complex I, decreased the NOX levels in cerebral ischemia established by suture-occluded method. (3) Acupuncture reduced the necrosis dissolution of neuronal cells and meningeal edema, while promoting angiogenesis. (4) Quantitative immunohistochemical staining results showed acupuncture can increase the expression of AMPK, p-AMPK and the mitochondrial transcription factor PGC-1α, NRF2, TFAM and uncoupling protein 2 (UCP2). Meanwhile, acupuncture treatment up-regulated the expression of the corresponding protein. (5) Subsequently, acupuncture enhanced AMPK phosphorylation as well as the expression of PGC-1α, NRF2, TFAM and UCP2, implicated in mitochondrial synthesis and cellular apoptosis. (6) Finally, injections of AMPK antagonists and activators confirmed AMPK as a therapeutic target for the anti-nerve damage effects of acupuncture.Acupuncture intervention relieved ischemic stroke progression in MCAO rats by promoting energy metabolism and mitochondrial biogenesis in the brain and alleviating neuronal apoptosis, which was mediated by eliciting AMPK/PGC-1α axis, among them AMPK is a therapeutic target.
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