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本文引用的文献

1
Electroacupuncture attenuates ferroptosis by promoting Nrf2 nuclear translocation and activating Nrf2/SLC7A11/GPX4 pathway in ischemic stroke.电针通过促进Nrf2核转位并激活缺血性脑卒中中的Nrf2/SLC7A11/GPX4通路来减轻铁死亡。
Chin Med. 2025 Jan 4;20(1):4. doi: 10.1186/s13020-024-01047-0.
2
Isoliquiritigenin alleviates cerebral ischemia-reperfusion injury by reducing oxidative stress and ameliorating mitochondrial dysfunction via activating the Nrf2 pathway.异甘草素通过激活 Nrf2 通路减轻氧化应激和改善线粒体功能障碍来减轻脑缺血再灌注损伤。
Redox Biol. 2024 Nov;77:103406. doi: 10.1016/j.redox.2024.103406. Epub 2024 Oct 22.
3
The gut lactic acid bacteria metabolite, 10-oxo--6,-11-octadecadienoic acid, suppresses inflammatory bowel disease in mice by modulating the NRF2 pathway and GPCR-signaling.肠道乳酸菌代谢产物 10-氧代-6,11-十八碳二烯酸通过调节 NRF2 通路和 GPCR 信号抑制小鼠炎症性肠病。
Front Immunol. 2024 Apr 30;15:1374425. doi: 10.3389/fimmu.2024.1374425. eCollection 2024.
4
ZMYND8 protects breast cancer stem cells against oxidative stress and ferroptosis through activation of NRF2.ZMYND8 通过激活 NRF2 保护乳腺癌干细胞免受氧化应激和铁死亡。
J Clin Invest. 2024 Jan 23;134(6):e171166. doi: 10.1172/JCI171166.
5
Saikosaponin A and D attenuate skeletal muscle atrophy in chronic kidney disease by reducing oxidative stress through activation of PI3K/AKT/Nrf2 pathway.柴胡皂苷 A 和 D 通过激活 PI3K/AKT/Nrf2 通路减少氧化应激从而减轻慢性肾脏病骨骼肌萎缩。
Phytomedicine. 2023 Jun;114:154766. doi: 10.1016/j.phymed.2023.154766. Epub 2023 Mar 21.
6
Electroacupuncture and human iPSC-derived small extracellular vesicles regulate the gut microbiota in ischemic stroke the brain-gut axis.电针和人诱导多能干细胞衍生的小细胞外囊泡调节缺血性脑卒中的肠道微生物群-脑肠轴。
Front Immunol. 2023 Jan 20;14:1107559. doi: 10.3389/fimmu.2023.1107559. eCollection 2023.
7
Angong Niuhuang Pill ameliorates cerebral ischemia/reperfusion injury in mice partly by restoring gut microbiota dysbiosis.安宫牛黄丸部分通过恢复肠道微生物群失调来改善小鼠脑缺血/再灌注损伤。
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8
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9
Silencing lncRNA SLC16A1-AS1 Induced Ferroptosis in Renal Cell Carcinoma Through miR-143-3p/SLC7A11 Signaling.沉默长链非编码 RNA SLC16A1-AS1 通过 miR-143-3p/SLC7A11 信号通路诱导肾细胞癌发生铁死亡。
Technol Cancer Res Treat. 2022 Jan-Dec;21:15330338221077803. doi: 10.1177/15330338221077803.
10
Dexmedetomidine exerts cerebral protective effects against cerebral ischemic injury by promoting the polarization of M2 microglia via the Nrf2/HO-1/NLRP3 pathway.右美托咪定通过 Nrf2/HO-1/NLRP3 通路促进 M2 小胶质细胞极化,发挥对脑缺血损伤的脑保护作用。
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[电针预处理通过肠-脑轴和Nrf2/HO-1信号通路抑制铁死亡减轻大鼠脑缺血再灌注损伤]

[Electroacupuncture pretreatment alleviates cerebral ischemia-reperfusion injury in rats by inhibiting ferroptosis through the gut-brain axis and the Nrf2/HO-1 signaling pathway].

作者信息

Zhang Anbang, Sun Xiuqi, Pang Bo, Wu Yuanhua, Shi Jingyu, Zhang Ning, Ye Tao

机构信息

Department of Neurology, First Affiliated Hospital of Guizhou University of Traditional Chinese Medicine, Guiyang 550001, China.

Department of Pharmacy, First Affiliated Hospital of Guizhou University of Traditional Chinese Medicine, Guiyang 550001, China.

出版信息

Nan Fang Yi Ke Da Xue Xue Bao. 2025 May 20;45(5):911-920. doi: 10.12122/j.issn.1673-4254.2025.05.03.

DOI:10.12122/j.issn.1673-4254.2025.05.03
PMID:40415422
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12104739/
Abstract

OBJECTIVES

To investigate the neuroprotective effects of electroacupuncture (EA) preconditioning against cerebral ischemia-reperfusion injury (CIRI) mediated by gut microbiota modulation, Nrf2/HO-1 pathway activation, and ferroptosis suppression.

METHODS

Adult male SD rats were divided into sham operation group, CIRI model group, and EA preconditioning group. In the latter two groups, rat models of CIRI were established by middle cerebral artery occlusion (MCAO), and in EA preconditioning group, EA was applied at Baihui (DU20) and Zusanli (ST36) for 3 days before modeling. Neurological deficits, cerebral infarction, and hippocampal pathology of the rats were evaluated using behavioral tests, TTC staining, and Nissl and HE staining, and the oxidative stress markers (MDA, ROS, and SOD), apoptosis/ferroptosis-related proteins (Bax, Bcl-2, GPX4, and SLC7A11), and changes in gut microbiota were analyzed.

RESULTS

EA preconditioning significantly reduced neurological deficits, decreased infarct volume, promoted hippocampal neuronal survival, and improved structural integrity of the hippocampal neurons in MCAO rats. EA preconditioning also significantly lowered MDA and ROS and increased SOD levels, upregulated Bcl-2, GPX4, and SLC7A11 expressions, and downregulated Bax expression in the hippocampal tissue of the rats, causing also activation of Nrf2/HO-1 signaling and improvement of gut microbiota composition.

CONCLUSIONS

EA preconditioning alleviates CIRI in rats by suppressing ferroptosis and apoptosis, enhancing antioxidant defenses via activating Nrf2/HO-1 signaling, and regulating the gut-brain axis.

摘要

目的

探讨电针预处理通过调节肠道菌群、激活Nrf2/HO-1通路和抑制铁死亡介导的对脑缺血再灌注损伤(CIRI)的神经保护作用。

方法

成年雄性SD大鼠分为假手术组、CIRI模型组和电针预处理组。后两组采用大脑中动脉闭塞(MCAO)法建立CIRI大鼠模型,电针预处理组在造模前3天于百会(DU20)和足三里(ST36)施加电针。采用行为学测试、TTC染色以及尼氏染色和苏木精-伊红染色评估大鼠的神经功能缺损、脑梗死和海马病理情况,并分析氧化应激标志物(丙二醛、活性氧和超氧化物歧化酶)、凋亡/铁死亡相关蛋白(Bax、Bcl-2、谷胱甘肽过氧化物酶4和溶质载体家族7成员11)以及肠道菌群的变化。

结果

电针预处理显著降低了MCAO大鼠的神经功能缺损,减小了梗死体积,促进了海马神经元存活,并改善了海马神经元的结构完整性。电针预处理还显著降低了大鼠海马组织中的丙二醛和活性氧水平,提高了超氧化物歧化酶水平,上调了Bcl-2、谷胱甘肽过氧化物酶4和溶质载体家族7成员11的表达,下调了Bax表达,同时还激活了Nrf2/HO-1信号通路并改善了肠道菌群组成。

结论

电针预处理通过抑制铁死亡和凋亡、激活Nrf2/HO-1信号通路增强抗氧化防御以及调节肠-脑轴来减轻大鼠的CIRI。