Electroacupuncture Inhibits Ferroptosis Induced by Cerebral Ischemiareperfusion

电针 自噬 细胞凋亡 免疫印迹 程序性细胞死亡 活性氧 医学 氧化应激 线粒体 药理学 冲程(发动机) 坏死性下垂 化学 生物 病理 内科学 细胞生物学 针灸科 生物化学 基因 工程类 替代医学 机械工程
作者
Guiling Wang,Shu-Ying Xu,He-Qun Lv,Chao Zhang,Yong-Jun Peng
出处
期刊:Current Neurovascular Research [Bentham Science Publishers]
卷期号:20 (3): 346-353 被引量:18
标识
DOI:10.2174/1567202620666230623153728
摘要

Electroacupuncture (EA) treatment has been recommended by World Health Organization (WHO) for years on cerebral ischemia treatment, but the specific mechanism is still elusive. Studies have shown that EA can relieve brain damage after ischemic stroke by inhibiting programmed cell death (PCD), such as apoptosis, necroptosis, and autophagy. Ferroptosis, a unique form of cell death, has been highlighted recently and found to occur in I/R injury. We, therefore, investigated whether EA plays an essential role in relieving cerebral I/R injury via ferroptosis.The modified MCAO/R rats model was established and then divided into four groups with or without EA treatment. Neurological deficit score and TTC staining were used to evaluate the neurological deficit and infarct volume of each group. Transmission electron microscope (TEM) and immunofluorescence staining were applied for mitochondrial ultrastructure and ROS accumulation observation, respectively. The proteins and mRNA expression of ACSL4, TFR1, and GPX4 were assessed by western blot and qPCR to detect the progress of ferroptosis.EA treatment improved neurological deficits and reduced infarct volume. Moreover, EA significantly relieved the mitochondrial morphological changes and inhibited ROS Production in MCAO rats. In terms of its mechanism, EA obviously decreased the ACSL4 and TFR1 expressions and promoted GPX4 levels in MCAO/R model rats.These findings indicate that EA might play an essential role in relieving cerebral I/R injury via ferroptosis.
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