Liu Ji, Han Ying, Wu Zhiyun, Chen Manli, Wu Wenwen, Zhao Zijun, Yuan Jinjin, Zheng Zhijian, Lin Qiang, Liu Nan, Chen Hongbin
Department of Neurology, Fujian Medical University Union Hospital, Fuzhou, China; Department of Rehabilitation, Fujian Medical University Union Hospital, Fuzhou, China; Fujian Key Laboratory of Molecular Neurology, Fujian Medical University, Fuzhou, China; Institute of Clinical Neurology, Fujian Medical University, Fuzhou, China.
Department of Geriatrics, Fujian Medical University Union Hospital, Fuzhou, China.
Phytomedicine. 2025 Jan;136:156328. doi: 10.1016/j.phymed.2024.156328. Epub 2024 Dec 15.
Perilladehyde, an extract of perillae in the Labiatae family, can produce significant anti-inflammatory and antioxidant effects. Although literature evidences the favorable effect of perillaldehyde on ischemic stroke, the exact mechanism remains blurred.
This study attempted to explore the impact of perillaldehyde on cerebral ischemia-reperfusion injury and the related action mechanism.
The rat tMCAO and neuronal OGD/R models were established to simulate cerebral ischemia-reperfusion injury. Lentiviruses were used to interfere with the expression of Nrf2 and Trx2 in neurons. The effects and action mechanisms of perillaldehyde were explored by various experimental methods, including chromatin immunoprecipitation assay, Western Blot, flow cytometry, dual-luciferase reporter gene assay, transmission electron microscopy, MRI, RNA-seq, and immunofluorescence staining.
Perillaldehyde pretreatment effectively mitigated the tMCAO-induced brain injury in rats by reducing cerebral infarction, improving neuromotor function, and attenuating cell apoptosis in the ischemic penumbra. In vitro, perillaldehyde pretreatment alleviated cell death and excessive oxidative stress, preserved the mitochondrial membrane integrity, enhanced mitochondrial energy metabolism, and facilitated the restoration of mitochondrial ultrastructure after OGD/R. The mechanism probe revealed that perillaldehyde activated the Nrf2/Keap1/Trx2 signaling axis, thus promoting the transcription of Trx2 and improving mitochondrial structure and function. The aforementioned impacts of perillaldehyde were somewhat counteracted by disrupting the expression of Nrf2 and Trx2, suggesting that the neuroprotection of perillaldehyde partially involves the activation of the Nrf2/Keap1/Trx2 axis.
This study firstly demonstrates the existence of the Nrf2/Keap1/Trx2 signaling axis in cerebral ischemia-reperfusion injury and evidences that perillaldehyde pretreatment can promote the restoration of neuronal mitochondrial structure and function by activating the Nrf2/Keap1/Trx2 axis after cerebral ischemia-reperfusion injury. These findings signify that perillaldehyde holds great promises for clinical management of ischemic stroke.
紫苏醛是唇形科紫苏属植物的提取物,具有显著的抗炎和抗氧化作用。尽管文献证实了紫苏醛对缺血性中风有有益作用,但其确切机制仍不清楚。
本研究旨在探讨紫苏醛对脑缺血再灌注损伤的影响及其相关作用机制。
建立大鼠大脑中动脉闭塞(tMCAO)和神经元氧糖剥夺/复氧(OGD/R)模型以模拟脑缺血再灌注损伤。利用慢病毒干扰神经元中Nrf2和Trx2的表达。通过多种实验方法,包括染色质免疫沉淀分析、蛋白质免疫印迹法、流式细胞术、双荧光素酶报告基因检测、透射电子显微镜、磁共振成像、RNA测序和免疫荧光染色,探讨紫苏醛的作用及其机制。
紫苏醛预处理通过减少脑梗死、改善神经运动功能和减轻缺血半暗带细胞凋亡,有效减轻了tMCAO诱导的大鼠脑损伤。在体外,紫苏醛预处理减轻了细胞死亡和过度氧化应激,维持了线粒体膜的完整性,增强了线粒体能量代谢,并促进了OGD/R后线粒体超微结构的恢复。机制研究表明,紫苏醛激活了Nrf2/Keap1/Trx2信号轴,从而促进Trx2的转录,改善线粒体结构和功能。干扰Nrf2和Trx2的表达部分抵消了紫苏醛的上述作用,表明紫苏醛的神经保护作用部分涉及Nrf2/Keap1/Trx2轴的激活。
本研究首次证明了脑缺血再灌注损伤中存在Nrf2/Keap1/Trx2信号轴,并证实紫苏醛预处理可通过激活脑缺血再灌注损伤后的Nrf2/Keap1/Trx2轴促进神经元线粒体结构和功能的恢复。这些发现表明紫苏醛在缺血性中风的临床治疗中具有很大的应用前景。