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Protein Drug Targets of Lavandula angustifolia on treatment of Rat Alzheimers Disease

机译:薰衣草的蛋白药物靶向治疗大鼠阿尔茨海默氏病

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摘要

Different treatment strategies of Alzheimer's disease (AD) are being studied for treating or slowing the progression of AD. Many pharmaceutically important regulation systems operate through proteins as drug targets. Here, we investigate the drug target proteins in beta-amyloid (Aβ) injected rat hippocampus treated with Lavandula angustifolia (LA) by proteomics techniques. The reported study showed that lavender extract (LE) improves the spatial performance in AD animal model by diminishing Aβ production in histopathology of hippocampus, so in this study neuroprotective proteins expressed in Aβ injected rats treated with LE were scrutinized. Rats were divided into three groups including normal, Aβ injected, and Aβ injected that was treated with LE. Protein expression profiles of hippocampus tissue were determined by two-dimensional electrophoresis (2DE) method and dysregulated proteins such as Snca, NF-L, Hspa5, Prdx2, Apoa1, and Atp5a1were identified by MALDI-TOF/TOF. KEGG pathway and gene ontology (GO) categories were used by searching DAVID Bioinformatics Resources. All detected protein spots were used to determine predictedinteractions with other proteins in STRING online database. Different isoforms of important protein, Snca that exhibited neuroprotective effects by anti-apoptotic properties were expressed. NF-L involved in the maintenance of neuronal caliber. Hspa5 likewise Prdx2 displays as anti-apoptotic protein that Prdx2 also involved in the neurotrophic effects. Apoa1 has anti-inflammatory activity and Atp5a1, produces ATP from ADP. To sum up, these proteins as potential drug targets were expressed in hippocampus in response to effective components in LA may have therapeutic properties for the treatment of AD and other neurodegenerative diseases.
机译:为了治疗或减缓AD的发展,正在研究阿尔茨海默氏病(AD)的不同治疗策略。许多药学上重要的调节系统通过蛋白质作为药物靶标起作用。在这里,我们通过蛋白质组学技术研究用薰衣草(LA)处理过的大鼠海马中注射β-淀粉样蛋白(Aβ)的药物靶蛋白。报道的研究表明,薰衣草提取物(LE)可通过减少海马组织病理学中的Aβ产生来改善AD动物模型的空间性能,因此本研究中对经LE处理的Aβ注射大鼠中表达的神经保护蛋白进行了研究。将大鼠分成三组,包括正常,注射Aβ和用LE治疗的注射Aβ。通过二维电泳(2DE)方法确定海马组织的蛋白表达谱,并通过MALDI-TOF / TOF鉴定失调的蛋白,例如Snca,NF-L,Hspa5,Prdx2,Apoa1和Apt5a1。通过搜索DAVID Bioinformatics Resources,使用了KEGG途径和基因本体论(GO)类别。在STRING在线数据库中,所有检测到的蛋白质斑点均用于确定与其他蛋白质的预测相互作用。表达了重要蛋白Snca的不同同工型,这些蛋白通过抗凋亡特性表现出神经保护作用。 NF-L参与神经元口径的维持。 Hspa5同样将Prdx2显示为抗凋亡蛋白,而Prdx2也参与了神经营养作用。 Apoa1具有抗炎活性,而Atp5a1具有ADP产生的ATP。综上所述,这些蛋白质作为潜在的药物靶点,是响应于LA中的有效成分而在海马中表达的,可能具有治疗AD和其他神经退行性疾病的治疗特性。

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