四氢小檗碱激活Nrf2信号通路抑制铁下垂并促进脊髓损伤后功能恢复。

IF 4.6 2区 医学 Q1 NEUROSCIENCES
Molecular Neurobiology Pub Date : 2025-07-01 Epub Date: 2025-02-26 DOI:10.1007/s12035-025-04791-y
Xiang Li, Heng Yu, Rongjie Liu, Jiansen Miao, Junlei Lv, Shu Yang, Yuxuan Zhu, Yan Chen, Keyu Lu, Chongan Huang, Xiangyang Wang
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引用次数: 0

摘要

最近的研究发现,铁上吊是一种新发现的程序性细胞死亡形式,是脊髓损伤(SCI)的一个重要因素。四氢小檗碱(Tetrahydroberberine, THB)是一种四氢异喹啉生物碱,从罂粟科植物延胡索的块茎中提取,具有抗氧化和神经保护作用。尽管有这些特性,THB对脊髓损伤的潜在保护作用仍有待深入研究。因此,本研究的目的是阐明THB对脊髓损伤的保护作用及其作用机制。采用小鼠脊髓损伤模型进行体内实验。使用Basso小鼠评分(BMS)、足迹分析、苏木精和伊红(HE)、马松三色和尼索尔染色来评估功能恢复。脂质过氧化用丙二醛(MDA)、谷胱甘肽(GSH)和超氧化物歧化酶(SOD)进行定量。采用western blot (WB)和免疫荧光(IF)染色分析核因子-红细胞2相关因子2 (Nrf2)信号通路和铁凋亡标志物的表达水平。为了进一步阐明THB抑制铁下垂的机制,我们利用已知的铁下垂激活剂RSL3在PC12细胞中建立了体外铁下垂模型。四氢大麻酚显著改善脊髓损伤后小鼠的组织和运动功能恢复,与对照组相比,BMS评分提高了约50%。脂质过氧化实验显示THB显著降低MDA水平,增加GSH和SOD水平。体内和体外实验均表明,THB可显著激活Nrf2通路,抑制小鼠和PC12细胞的铁下垂。这种保护作用被Nrf2抑制剂ML385逆转,这可以通过抑制Nrf2途径、增加脂质过氧化和提高铁下垂水平来证明。我们的体内和体外实验表明,THB通过激活Nrf2信号通路促进脊髓损伤后的功能恢复,从而减轻脂质过氧化,抑制铁质凋亡,从而促进神经元存活。我们的研究结果有助于更全面地了解THB如何在脊髓损伤中发挥其恢复作用,并证明THB作为脊髓损伤临床治疗的新治疗策略的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Activation of the Nrf2 Signaling Pathway by Tetrahydroberberine Suppresses Ferroptosis and Enhances Functional Recovery Following Spinal Cord Injury.

Recent research has identified ferroptosis, a newly recognized form of programmed cell death, is a crucial factor in spinal cord injury (SCI). Tetrahydroberberine (THB) is a tetrahydroisoquinoline alkaloid derived from the tuber of the poppy family plant, Corydalis, which is recognized for its antioxidant and neuroprotective properties. Despite these attributes, the potential protective effects of THB against SCI are yet to be thoroughly investigated. Therefore, the aim of this study was to elucidate the protective effects and underlying mechanisms of action of THB in SCI. A mouse model of SCI was used for the in vivo experiments. Functional recovery was evaluated using the Basso Mouse Scale (BMS), footprint analysis, and hematoxylin and eosin (HE), Masson's trichrome, and Nissl staining. Lipid peroxidation was quantified using malondialdehyde (MDA), glutathione (GSH), and superoxide dismutase (SOD). The expression levels of the nuclear factor erythroid 2-related factor 2 (Nrf2) signaling pathway and ferroptosis markers were analyzed using western blot (WB) and immunofluorescence (IF) staining. To further elucidate the mechanism through which THB inhibits ferroptosis, an in vitro ferroptosis model was established in PC12 cells using RSL3, a known ferroptosis activator. THB markedly improved tissue and motor function restoration in mice post-SCI, with the BMS score increasing by approximately 50% compared with that in the control group. Lipid peroxidation assays revealed that THB significantly reduced MDA levels and increased GSH and SOD levels. Both in vivo and in vitro experiments demonstrated that THB significantly activated the Nrf2 pathway and inhibited ferroptosis in mice and in PC12 cells. This protective effect was reversed by the Nrf2 inhibitor, ML385, as evidenced by suppression of the Nrf2 pathway, increased lipid peroxidation, and elevated ferroptosis levels. Our in vivo and in vitro experiments indicate that THB promotes functional recovery after SCI by activating the Nrf2 signaling pathway, which attenuates lipid peroxidation and suppresses ferroptosis, thereby contributing to neuronal survival. Our findings contribute to a more comprehensive understanding of how THB exerts its recovery effects in SCI and demonstrate the potential of THB as a novel therapeutic strategy for the clinical management of SCI.

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来源期刊
Molecular Neurobiology
Molecular Neurobiology 医学-神经科学
CiteScore
9.00
自引率
2.00%
发文量
480
审稿时长
1 months
期刊介绍: Molecular Neurobiology is an exciting journal for neuroscientists needing to stay in close touch with progress at the forefront of molecular brain research today. It is an especially important periodical for graduate students and "postdocs," specifically designed to synthesize and critically assess research trends for all neuroscientists hoping to stay active at the cutting edge of this dramatically developing area. This journal has proven to be crucial in departmental libraries, serving as essential reading for every committed neuroscientist who is striving to keep abreast of all rapid developments in a forefront field. Most recent significant advances in experimental and clinical neuroscience have been occurring at the molecular level. Until now, there has been no journal devoted to looking closely at this fragmented literature in a critical, coherent fashion. Each submission is thoroughly analyzed by scientists and clinicians internationally renowned for their special competence in the areas treated.
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