恢复大脑健康:电针 GB20 和 LR3,通过恢复线粒体缓解偏头痛。

IF 2.3 4区 医学 Q3 CLINICAL NEUROLOGY Brain Circulation Pub Date : 2024-06-26 eCollection Date: 2024-04-01 DOI:10.4103/bc.bc_95_23
Jianchang Luo, Liyao Feng, Luodan Wang, Zhenyu Fang, Jiawang Lang, Boxu Lang
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引用次数: 0

摘要

背景:电针(EA)是治疗偏头痛的一种很有前景的替代疗法,线粒体功能障碍被认为是偏头痛病理生理学的一个关键机制。本研究旨在探讨电针治疗偏头痛的潜力,并揭示与线粒体异常相关的机制:用 10 毫克/千克硝酸甘油诱导大鼠偏头痛,然后在 GB20 和 LR3 处进行 2/15 赫兹的 EA 治疗。通过摄像头记录痛觉行为,并使用 EthoVision XT 12.0 软件进行分析。使用 von Frey 试验评估后爪抽离阈值。我们使用免疫组织化学和酶联免疫吸附试验评估了降钙素基因相关肽(CGRP)、一氧化氮(NO)和内皮素(ET)的水平--它们是偏头痛病理生理学的关键参数。透射电子显微镜观察了脑组织中线粒体的形态。流式细胞术测量了线粒体中的活性氧(ROS)水平。通过 Western 印迹分析评估了 PINK1 和 Parkin 的水平:结果:GB20和LR3的EA降低了偏头痛大鼠的痛觉行为(休息和梳理),增加了探索和运动行为。EA治疗后,偏头痛大鼠的后爪抽离阈值显著升高。EA 治疗后,CGRP 和 NO 水平下降,而 ET 水平上升,这表明疼痛和血管生理发生了改变。值得注意的是,EA 治疗减轻了偏头痛大鼠脑组织中线粒体的损伤,降低了 ROS 水平。EA 治疗可上调偏头痛大鼠 PINK1 和 Parkin 的表达:GB20和LR3的EA可通过缓解PINK1/Parkin介导的线粒体功能障碍来治疗偏头痛。
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Restoring brain health: Electroacupuncture at GB20 and LR3 for migraine mitigation through mitochondrial restoration.

Background: Electroacupuncture (EA) is a promising alternative therapy for migraine, with mitochondrial dysfunction hypothesized as a pivotal mechanism in migraine pathophysiology. This research endeavors to investigate the therapeutic potential of EA in addressing migraines and shed light on the associated mechanisms linked to mitochondrial anomalies.

Materials and methods: Migraine in rats was induced by 10 mg/kg nitroglycerin, followed by 2/15 Hz EA treatment at GB20 and LR3. Nociceptive behavior was recorded via a camera and analyzed using EthoVision XT 12.0 software. The hind-paw withdrawal threshold was assessed using the von Frey test. We assessed the levels of calcitonin gene-related peptide (CGRP), nitric oxide (NO), and endothelin (ET) - key parameters in migraine pathophysiology using immunohistochemistry and enzyme-linked immunosorbent assay. Mitochondrial morphology in brain tissues was observed through transmission electron microscopy. Reactive oxygen species (ROS) level in mitochondria was measured by flow cytometry. The levels of PINK1 and Parkin were assessed using Western blot analysis.

Results: EA at GB20 and LR3 decreased nociceptive behaviors (resting and grooming) and increased exploratory and locomotor behaviors in migraine rats. The hind-paw withdrawal threshold in migraine rats was significantly elevated following EA treatment. Post-EA treatment, levels of CGRP and NO decreased, while ET level increased, suggesting an alteration in pain and vascular physiology. Notably, EA treatment mitigated the mitochondrial damage and reduced ROS level in the brain tissues of migraine rats. EA treatment upregulated the expression of PINK1 and Parkin in migraine rats.

Conclusion: EA at GB20 and LR3 may treat migraine by alleviating PINK1/Parkin-mediated mitochondrial dysfunction.

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来源期刊
Brain Circulation
Brain Circulation Multiple-
自引率
5.30%
发文量
31
审稿时长
16 weeks
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