电针抑制脑缺血灌注诱发的铁下垂。

IF 2 4区 医学 Q3 CLINICAL NEUROLOGY
Gui-Ling Wang, Shu-Ying Xu, He-Qun Lv, Chao Zhang, Yong-Jun Peng
{"title":"电针抑制脑缺血灌注诱发的铁下垂。","authors":"Gui-Ling Wang,&nbsp;Shu-Ying Xu,&nbsp;He-Qun Lv,&nbsp;Chao Zhang,&nbsp;Yong-Jun Peng","doi":"10.2174/1567202620666230623153728","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>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.</p><p><strong>Methods: </strong>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.</p><p><strong>Results: </strong>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.</p><p><strong>Conclusion: </strong>These findings indicate that EA might play an essential role in relieving cerebral I/R injury via ferroptosis.</p>","PeriodicalId":10879,"journal":{"name":"Current neurovascular research","volume":"20 3","pages":"346-353"},"PeriodicalIF":2.0000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Electroacupuncture Inhibits Ferroptosis Induced by Cerebral Ischemiareperfusion.\",\"authors\":\"Gui-Ling Wang,&nbsp;Shu-Ying Xu,&nbsp;He-Qun Lv,&nbsp;Chao Zhang,&nbsp;Yong-Jun Peng\",\"doi\":\"10.2174/1567202620666230623153728\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>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.</p><p><strong>Methods: </strong>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.</p><p><strong>Results: </strong>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.</p><p><strong>Conclusion: </strong>These findings indicate that EA might play an essential role in relieving cerebral I/R injury via ferroptosis.</p>\",\"PeriodicalId\":10879,\"journal\":{\"name\":\"Current neurovascular research\",\"volume\":\"20 3\",\"pages\":\"346-353\"},\"PeriodicalIF\":2.0000,\"publicationDate\":\"2023-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Current neurovascular research\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.2174/1567202620666230623153728\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CLINICAL NEUROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current neurovascular research","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.2174/1567202620666230623153728","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 1

摘要

背景:世界卫生组织(世界卫生组织)多年来一直推荐电针治疗脑缺血,但其具体机制尚不明确。研究表明,电针可以通过抑制程序性细胞死亡(PCD),如细胞凋亡、坏死和自噬,减轻缺血性中风后的脑损伤。脱铁症是一种独特的细胞死亡形式,最近得到了重视,并被发现发生在I/R损伤中。因此,我们研究了电针是否通过脱铁作用在减轻脑I/R损伤中发挥重要作用。方法:建立改良MCAO/R大鼠模型,分为电针组和不电针组。使用神经功能缺损评分和TTC染色来评估各组的神经功能缺损和梗死体积。透射电镜(TEM)和免疫荧光染色分别观察线粒体超微结构和ROS积累。通过蛋白质印迹和qPCR评估ACSL4、TFR1和GPX4的蛋白质和mRNA表达,以检测脱铁性贫血的进展。结果:电针治疗改善了神经功能缺损,减少了梗死体积。此外,电针显著减轻MCAO大鼠线粒体形态变化,抑制ROS的产生。就其机制而言,电针可明显降低MCAO/R模型大鼠ACSL4和TFR1的表达,提高GPX4的水平。结论:电针在减轻脑缺血再灌注损伤中可能发挥重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Electroacupuncture Inhibits Ferroptosis Induced by Cerebral Ischemiareperfusion.

Background: 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.

Methods: 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.

Results: 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.

Conclusion: These findings indicate that EA might play an essential role in relieving cerebral I/R injury via ferroptosis.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Current neurovascular research
Current neurovascular research 医学-临床神经学
CiteScore
3.80
自引率
9.50%
发文量
54
审稿时长
3 months
期刊介绍: Current Neurovascular Research provides a cross platform for the publication of scientifically rigorous research that addresses disease mechanisms of both neuronal and vascular origins in neuroscience. The journal serves as an international forum publishing novel and original work as well as timely neuroscience research articles, full-length/mini reviews in the disciplines of cell developmental disorders, plasticity, and degeneration that bridges the gap between basic science research and clinical discovery. Current Neurovascular Research emphasizes the elucidation of disease mechanisms, both cellular and molecular, which can impact the development of unique therapeutic strategies for neuronal and vascular disorders.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信