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

Q3 Medicine
Anbang Zhang, Xiuqi Sun, Bo Pang, Yuanhua Wu, Jingyu Shi, Ning Zhang, Tao Ye
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引用次数: 0

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.

[电针预处理通过肠脑轴和Nrf2/HO-1信号通路抑制铁下沉,减轻大鼠脑缺血再灌注损伤]。
目的:探讨电针(EA)预处理对肠道菌群调节、Nrf2/HO-1通路激活和抑制铁下沉介导的脑缺血再灌注损伤(CIRI)的神经保护作用。方法:将成年雄性SD大鼠分为假手术组、CIRI模型组和EA预处理组。后两组采用大脑中动脉闭塞法(MCAO)建立大鼠CIRI模型,EA预处理组在造模前在百会(DU20)和足三里(ST36)处应用EA 3 d。采用行为学测试、TTC染色、Nissl和HE染色评估大鼠神经功能缺损、脑梗死和海马病理变化,分析氧化应激标志物(MDA、ROS、SOD)、凋亡/铁中毒相关蛋白(Bax、Bcl-2、GPX4、SLC7A11)和肠道菌群变化。结果:EA预处理显著减少MCAO大鼠神经功能缺损,减少梗死体积,促进海马神经元存活,改善海马神经元结构完整性。EA预处理还能显著降低大鼠海马组织MDA、ROS、SOD水平,上调Bcl-2、GPX4、SLC7A11表达,下调Bax表达,激活Nrf2/HO-1信号,改善肠道菌群组成。结论:EA预处理可通过抑制铁凋亡、激活Nrf2/HO-1信号通路增强抗氧化防御能力、调节肠脑轴等途径减轻大鼠CIRI。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
南方医科大学学报杂志
南方医科大学学报杂志 Medicine-Medicine (all)
CiteScore
1.50
自引率
0.00%
发文量
208
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