奎尼酸调节海马神经发生:神经退行性疾病的治疗策略

IF 2.4 3区 医学 Q3 NEUROSCIENCES
Hippocampus Pub Date : 2024-08-06 DOI:10.1002/hipo.23630
Kanwal Iftikhar, Maryam Niaz, Maha Shahid, Sumbul Zehra, Taj Afzal, Shaheen Faizi, Shabana Usman Simjee
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引用次数: 0

摘要

神经祖细胞(NPCs)存在于大脑中,参与神经发生机制,使大脑能够生成增强认知能力和掌握新技能的基石。NPCs 在大脑中的存在为探索其治疗各种神经退行性疾病的潜力开辟了一个新的研究领域。本研究对奎尼酸(QA)调控神经元细胞增殖、成熟和分化的细胞内机制提供了新的见解。此外,这项研究可能有助于发现和开发先导分子,从而克服治疗神经退行性疾病的挑战。研究人员使用 MTT 试验研究了 QA 对生长的支持作用。分析了所选分子标记物 nestin、神经元特异性 III 类 beta-tubulin(Tuj-1)、神经元核蛋白(NeuN)、神经元分化 1(NeuroD1)、胶质纤维酸性蛋白(GFAP)、神经胶质蛋白(NLGN)和波形蛋白的基因和蛋白表达。QA诱导的海马祖细胞增殖和分化也伴随着祖细胞和未成熟神经元标志物、成熟神经元标志物和分化因子(即nestin、Tuj-1、NeuN和NeuroD1)的表达显著增加。另一方面,在 QA 处理后观察到波形蛋白下调和 GFAP 表达不变。此外,还利用体外氧葡萄糖剥夺(OGD)模型研究了 QA 对受压细胞恢复的影响。结果表明,海马细胞经 QA 处理后能从 OGD 中恢复。这些研究结果表明,QA 处理可通过促进 NPCs 的增殖和分化来促进海马神经发生,并使神经元从 OGD 引起的应激中恢复过来。因此,QA 的神经源潜力可用于治疗神经退行性疾病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hippocampal neurogenesis modulated by Quinic acid: A therapeutic strategy for the neurodegenerative disorders

Neural progenitor cells (NPCs) reside in the brain and participate in the mechanism of neurogenesis that permits the brain to generate the building blocks for enhancement of cognitive abilities and acquisition of new skills. The existence of NPCs in brain has opened a novel dimension of research to explore their potential for treatment of various neurodegenerative disorders. The present study provides novel insights into the intracellular mechanisms in neuronal cells proliferation, maturation and differentiation regulated by Quinic acid (QA). Furthermore, this study might help in discovery and development of lead molecule that can overcome the challenges in the treatment of neurodegenerative diseases. The growth supporting effect of QA was studied using MTT assay. For that purpose, hippocampal cell cultures of neonatal rats were treated with different concentrations of QA and incubated for 24, 48 and 72 h. Gene and protein expressions of the selected molecular markers nestin, neuron-specific class III beta-tubulin (Tuj-1), neuronal nuclear protein (NeuN), neuronal differentiation 1 (NeuroD1), glial fibrillary acidic protein (GFAP), neuroligin (NLGN) and vimentin were analyzed. QA-induced cell proliferation and differentiation of hippocampal progenitor cells was also accompanied by significantly increased expression of progenitor and immature neuronal marker, mature neuronal marker and differentiating factor, that is, nestin, Tuj-1, NeuN and NeuroD1, respectively. On the other hand, vimentin downregulation and constant GFAP expression were observed following QA treatment. Additionally, the effects of QA on the recovery of stressed cells was studied using in vitro model of oxygen glucose deprivation (OGD). It was observed that hippocampal cells were able to recover from OGD following the treatment with QA. These findings suggest that QA treatment promotes hippocampal neurogenesis by proliferating and differentiating of NPCs and recovers neurons from stress caused by OGD. Thus, the neurogenic potential of QA can be explored for the treatment of neurodegenerative disorders.

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来源期刊
Hippocampus
Hippocampus 医学-神经科学
CiteScore
5.80
自引率
5.70%
发文量
79
审稿时长
3-8 weeks
期刊介绍: Hippocampus provides a forum for the exchange of current information between investigators interested in the neurobiology of the hippocampal formation and related structures. While the relationships of submitted papers to the hippocampal formation will be evaluated liberally, the substance of appropriate papers should deal with the hippocampal formation per se or with the interaction between the hippocampal formation and other brain regions. The scope of Hippocampus is wide: single and multidisciplinary experimental studies from all fields of basic science, theoretical papers, papers dealing with hippocampal preparations as models for understanding the central nervous system, and clinical studies will be considered for publication. The Editor especially encourages the submission of papers that contribute to a functional understanding of the hippocampal formation.
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