通过激活 PI3K/Akt 信号通路促进脊髓损伤后的轴突再生和运动功能恢复

IF 3.5 3区 医学 Q2 NEUROSCIENCES
Yunyun Wang, Jiachun Lu, Hua Xiao, Lijuan Ding, Yongzhi He, Cong Chang, Wenchun Wang
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引用次数: 0

摘要

缬草(Valeriana jatamansi Jones,VJJ)在中国传统中药和民族医药中具有悠久的历史,常用于缓解脘腹胀痛、积食、泄泻、痢疾等肠胃不适以及失眠等疾病。此外,从 Valeriana jatamansi Jones 提取的富含铱化物的馏分(IRFV)在促进脊髓损伤(SCI)后的运动功能恢复方面也有疗效。本研究旨在探讨 IRFV 对 SCI 的治疗效果及其内在机制。首先,研究人员建立了脊髓损伤大鼠模型,以评估 IRFV 对轴突再生的影响。随后,利用 PC12 细胞氧化损伤模型,使用磷酸肌醇-3-激酶(PI3K)/蛋白激酶 B(Akt)信号通路抑制剂 LY294002 探索 IRFV 在促进轴突再生中的作用和机制。最后,给SCI大鼠注射了相同的抑制剂,以确认IRFV通过激活PI3K/Akt信号通路促进轴突再生的分子机制。结果表明,IRFV能显著增强SCI大鼠的运动功能恢复,减少病理损伤,促进轴突再生。体外实验显示,IRFV能提高PC12细胞的活力,促进轴突再生,并激活PI3K/Akt信号通路。值得注意的是,抑制这一途径会抵消 IRFV 对 SCI 大鼠的治疗效果。总之,IRFV可通过激活PI3K/Akt信号通路促进轴突再生,并促进脊髓损伤后运动功能的恢复。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Iridoids rich fraction from Valeriana jatamansi Jones promotes axonal regeneration and motor functional recovery after spinal cord injury through activation of the PI3K/Akt signaling pathway
Valeriana jatamansi Jones (VJJ), renowned for its extensive history in traditional Chinese medicine and ethnomedicine within China, is prevalently utilized to alleviate ailments such as epigastric distension and pain, gastrointestinal disturbances including food accumulation, diarrhea, and dysentery, as well as insomnia and other diseases. Moreover, the Iridoid-rich fraction derived from Valeriana jatamansi Jones (IRFV) has demonstrated efficacy in facilitating the recuperation of motor functions after spinal cord injury (SCI). This study is aimed to investigate the therapeutic effect of IRFV on SCI and its underlying mechanism. Initially, a rat model of SCI was developed to assess the impact of IRFV on axonal regeneration. Subsequently, employing the PC12 cell model of oxidative damage, the role and mechanism of IRFV in enhancing axonal regeneration were explored using the phosphoinositide-3-kinase (PI3K)/protein kinase B (Akt) signaling pathway inhibitor LY294002. Ultimately, the same inhibitor was administered to SCI rats to confirm the molecular mechanism through which IRFV promotes axonal regeneration by activating the PI3K/Akt signaling pathway. The results showed that IRFV significantly enhanced motor function recovery, reduced pathological injury, and facilitated axonal regeneration in SCI rats. In vitro experiments revealed that IRFV improved PC12 cell viability, augmented axonal regeneration, and activated the PI3K/Akt signaling pathway. Notably, the inhibition of this pathway negated the therapeutic benefits of IRFV in SCI rats. In conclusion, IRFV promote promotes axonal regeneration and recovery of motor function after SCI through activation of the PI3K/Akt signaling pathway.
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来源期刊
CiteScore
5.70
自引率
2.10%
发文量
669
审稿时长
14 weeks
期刊介绍: Frontiers in Molecular Neuroscience is a first-tier electronic journal devoted to identifying key molecules, as well as their functions and interactions, that underlie the structure, design and function of the brain across all levels. The scope of our journal encompasses synaptic and cellular proteins, coding and non-coding RNA, and molecular mechanisms regulating cellular and dendritic RNA translation. In recent years, a plethora of new cellular and synaptic players have been identified from reduced systems, such as neuronal cultures, but the relevance of these molecules in terms of cellular and synaptic function and plasticity in the living brain and its circuits has not been validated. The effects of spine growth and density observed using gene products identified from in vitro work are frequently not reproduced in vivo. Our journal is particularly interested in studies on genetically engineered model organisms (C. elegans, Drosophila, mouse), in which alterations in key molecules underlying cellular and synaptic function and plasticity produce defined anatomical, physiological and behavioral changes. In the mouse, genetic alterations limited to particular neural circuits (olfactory bulb, motor cortex, cortical layers, hippocampal subfields, cerebellum), preferably regulated in time and on demand, are of special interest, as they sidestep potential compensatory developmental effects.
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