猴面包树通过影响与白细胞介素 4、13 和阿尔茨海默病细胞外基质组织相关的信号通路来提供神经保护:基于蛋白质组学的视角

IF 4.4 3区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Neurochemistry international Pub Date : 2024-09-29 DOI:10.1016/j.neuint.2024.105864
Akhina Palollathil , Mohd Altaf Najar , S. Amrutha , Ravishankar Pervaje , Prashant Kumar Modi , Thottethodi Subrahmanya Keshava Prasad
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引用次数: 0

摘要

阿尔茨海默病是一种普遍存在于老年人中的神经退行性疾病,其特征是老年斑和神经纤维缠结的累积,引发氧化应激、神经炎症和神经元凋亡。目前的疗法侧重于对症治疗,而不是针对潜在的疾病改变分子机制,而且往往会产生严重的副作用。百服宁(Bacopa monnieri)是一种传统的印度草药,具有神经营养特性,自古以来就显示出治疗神经系统疾病的前景。然而,它在阿尔茨海默病中的作用机制仍然难以捉摸。在这项研究中,通过用β-淀粉样蛋白1-42肽(Aβ42)处理分化的IMR-32细胞,建立了阿尔茨海默病的细胞模型。此外,还通过与百忧解联合处理建立了一个恢复模型,以探索其保护机制。通过减少细胞凋亡和活性氧的产生,联合使用百服宁提取物可恢复 Aβ42 诱导的损伤。基于质谱的定量蛋白质组分析鉴定出了 21674 个肽段,对应于阿尔茨海默病模型中的 3626 个蛋白质。Aβ42调控失调的蛋白质与细胞功能有关,如细胞增殖负调控和微管细胞骨架组织。富集的途径包括细胞外基质组织以及白细胞介素-4和白细胞介素-13信号转导。百服宁联合治疗显示,Aβ42改变的蛋白质,包括FOSL1和TDO2,得到了显著的恢复。通过对单叶枯草恢复蛋白的蛋白-蛋白相互作用网络分析,确定了阿尔茨海默病的枢纽基因。这项研究的发现可能会为阿尔茨海默病的创新治疗方法开辟新的途径。
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Bacopa monnieri confers neuroprotection by influencing signaling pathways associated with interleukin 4, 13 and extracellular matrix organization in Alzheimer's disease: A proteomics-based perspective
Alzheimer's disease, a prevalent neurodegenerative disorder in the elderly, is characterized by the accumulation of senile plaques and neurofibrillary tangles, triggering oxidative stress, neuroinflammation, and neuronal apoptosis. Current therapies focus on symptomatic treatment rather than targeting the underlying disease-modifying molecular mechanisms and are often associated with significant side effects. Bacopa monnieri, a traditional Indian herb with nootropic properties, has shown promise in neurological disorder treatment from ancient times. However, its mechanisms of action in Alzheimer's disease remain elusive. In this study, a cellular model for Alzheimer's disease was created by treating differentiated IMR-32 cells with beta-amyloid, 1–42 peptide (Aβ42). Additionally, a recovery model was established through co-treatment with Bacopa monnieri to explore its protective mechanism. Co-treatment with Bacopa monnieri extract recovered Aβ42 induced damage as evidenced by the decreased apoptosis and reduced reactive oxygen species production. Mass spectrometry-based quantitative proteomic analysis identified 21,674 peptides, corresponding to 3626 proteins from the Alzheimer's disease model. The proteins dysregulated by Aβ42 were implicated in cellular functions, such as negative regulation of cell proliferation and microtubule cytoskeleton organization. The enriched pathways include extracellular matrix organization and interleukin-4 and interleukin-13 signaling. Bacopa monnieri co-treatment showed remarkable restoration of Aβ42 altered proteins, including FOSL1, and TDO2. The protein-protein interaction network analysis of Bacopa monnieri restored proteins identified the hub gene involved in Alzheimer's disease. The findings from this study may open up new avenues for creating innovative therapeutic approaches for Alzheimer's disease.
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来源期刊
Neurochemistry international
Neurochemistry international 医学-神经科学
CiteScore
8.40
自引率
2.40%
发文量
128
审稿时长
37 days
期刊介绍: Neurochemistry International is devoted to the rapid publication of outstanding original articles and timely reviews in neurochemistry. Manuscripts on a broad range of topics will be considered, including molecular and cellular neurochemistry, neuropharmacology and genetic aspects of CNS function, neuroimmunology, metabolism as well as the neurochemistry of neurological and psychiatric disorders of the CNS.
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