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电针通过恢复端粒酶逆转录酶改善脑缺血再灌注损伤后的神经元损伤和神经功能缺损。

Electroacupuncture Ameliorates Neuronal Damage and Neurological Deficits after Cerebral Ischemia-Reperfusion Injury via Restoring Telomerase Reverse Transcriptase.

作者信息

Chen Dan, Xiang Yunxia, Wu Di, Wang Hui, Huang Yaping, Xiao Hongbo

机构信息

Department of Rehabilitation Medicine, Xuancheng People's Hospital, Xuancheng, Anhui, China.

Department of Acupuncture and Moxibustion Rehabilitation, The First Affiliated Hospital of Anhui University of Chinese Medicine, Hefei, Anhui, China.

出版信息

Cell Biochem Biophys. 2025 Mar;83(1):717-727. doi: 10.1007/s12013-024-01504-5. Epub 2024 Sep 5.

Abstract

The purpose of this study is to identify the therapeutic effect of electroacupuncture (EA) on cerebral ischemia-reperfusion (I/R) injury, and to clarify the regulatory mechanism related to telomerase reverse transcriptase (TERT)-mediated telomerase activity. A Middle cerebral artery occlusion/reperfusion (MCAO/R) animal model was constructed and rats were treated by EA invention at the Baihui (GV20) and Fengchi (GB20) acupoints. Neurological deficits were assessed via rotarod test and Morris water maze test. 2,3,5-Triphenyltertrazolium chloride (TTC) staining was performed to evaluate infarct volume. Histological changes were observed under H&E staining and Nissl staining. TERT expression was examined using qRT-PCR and western blot. Telomerase activity was assessed with TRAP method. Neuron apoptosis and senescence were assessed by TUNEL and immunofluorescence assays. Inflammatory cytokines and oxidative stress-indicators were examined using commercial kits. EA intervention at both GV20 and GB20 acupoints reduced infarct volumes (2.48 ± 1.89 vs. 29.56 ± 2.55), elevated the telomerase activity (0.84 ± 0.08 vs. 0.34 ± 0.09), and upregulated the levels of total TERT protein (0.61 ± 0.09 vs. 0.21 ± 0.05) and mitochondrial TERT (Mito-TERT; 0.54 ± 0.03 vs. 0.27 ± 0.03) in hippocampus tissues of MCAO/R rats. EA intervention attenuated motor dysfunction (112.00 ± 6.69 vs. 30.02 ± 2.60) and improved spatial learning (23.87 ± 1.90 vs. 16.23 ± 1.45) and memory ability (8.38 ± 1.06 vs. 4.13 ± 1.13) of rats with cerebral I/R injury. In addition, EA intervention significantly attenuated histopathological changes of injured neurons, mitigated neuron apoptosis (32.27 ± 5.52 vs. 65.83 ± 4.31) and senescence in MCAO/R rats, as well as inhibited excessive production of inflammatory cytokines and attenuated oxidative stress. However, the above therapeutic efficiency of EA intervention in MCAO/R rats was partly eliminated by TERT knockdown. EA intervention at GB20 and GV20 acupoints exerted a protective role in cerebral I/R injury partly through restoring TERT function, implying the clinical potential of EA treatment in the treatment of ischemic stroke.

摘要

本研究旨在确定电针(EA)对脑缺血再灌注(I/R)损伤的治疗作用,并阐明与端粒酶逆转录酶(TERT)介导的端粒酶活性相关的调节机制。构建大脑中动脉闭塞/再灌注(MCAO/R)动物模型,对大鼠百会(GV20)和风池(GB20)穴位进行电针干预。通过转棒试验和Morris水迷宫试验评估神经功能缺损。采用2,3,5-氯化三苯基四氮唑(TTC)染色评估梗死体积。在苏木精-伊红(H&E)染色和尼氏染色下观察组织学变化。采用qRT-PCR和蛋白质免疫印迹法检测TERT表达。用端粒重复序列扩增法(TRAP)评估端粒酶活性。通过TUNEL和免疫荧光试验评估神经元凋亡和衰老。使用商用试剂盒检测炎性细胞因子和氧化应激指标。对GV20和GB20穴位进行电针干预可减小MCAO/R大鼠海马组织的梗死体积(2.48±1.89对29.56±2.55),提高端粒酶活性(0.84±0.08对0.34±0.09),并上调总TERT蛋白水平(0.61±0.09对0.21±0.05)和线粒体TERT(Mito-TERT;0.54±0.03对0.27±0.03)。电针干预可减轻MCAO/R大鼠的运动功能障碍(112.00±6.69对30.02±2.60),改善其空间学习能力(23.87±1.90对16.23±1.45)和记忆能力(8.38±1.06对4.13±1.13)。此外,电针干预可显著减轻MCAO/R大鼠受损神经元的组织病理学变化,减轻神经元凋亡(32.27±5.52对65.83±4.31)和衰老,还可抑制炎性细胞因子的过度产生并减轻氧化应激。然而,TERT基因敲低部分消除了电针干预对MCAO/R大鼠的上述治疗效果。对GB20和GV20穴位进行电针干预通过恢复TERT功能,对脑I/R损伤发挥了保护作用,这意味着电针治疗在缺血性脑卒中治疗中具有临床应用潜力。

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