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