Multimodal beneficial effects of BNN27, a nerve growth factor synthetic mimetic, in the 5xFAD mouse model of Alzheimer’s disease

IF 9.6 1区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecular Psychiatry Pub Date : 2024-11-25 DOI:10.1038/s41380-024-02833-w
Maria Kokkali, Kanelina Karali, Evangelia Thanou, Maria Anna Papadopoulou, Ioanna Zota, Alexandros Tsimpolis, Paschalis Efstathopoulos, Theodora Calogeropoulou, Ka Wan Li, Kyriaki Sidiropoulou, Achille Gravanis, Ioannis Charalampopoulos
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Abstract

Alzheimer’s Disease (AD) is an incurable and debilitating progressive, neurodegenerative disorder which is the leading cause of dementia worldwide. Neuropathologically, AD is characterized by the accumulation of Aβ amyloid plaques in the microenvironment of brain cells and neurovascular walls, chronic neuroinflammation, resulting in neuronal and synaptic loss, myelin and axonal failure, as well as significant reduction in adult hippocampal neurogenesis. The hippocampal formation is particularly vulnerable to this degenerative process, due to early dysfunction of the cholinergic circuit. Neurotrophic factors consist major regulatory molecules and their decline in AD is considered as an important cause of disease onset and progression. Novel pharmacological approaches are targeting the downstream pathways controlled by neurotrophins, such as nerve growth factor (NGF) receptors, TrkA and p75NTR, which enhance hippocampal neurogenic capacity and neuroprotective mechanisms, and potentially counteract the neurotoxic effects of amyloid deposition. BNN27 is a non-toxic, newly developed 17-spiro-steroid analog, penetrating the blood-brain-barrier (BBB) and mimicking the neuroprotective effects of NGF, acting as selective activator of its receptors, both TrkA and p75NTR, thus promoting survival of various neuronal cell types. Our present research aims at determining whether and which aspects of the AD-related pathology, BNN27 is able to alleviate, exploring the cellular and molecular AD components and link these changes with improvements in the cognitive performance of an animal AD model, the 5xFAD mice. Our results clearly indicate that BNN27 administration significantly reduced amyloid-β load in whole brain of the animals, enhanced adult hippocampal neurogenesis, restored cholinergic function and synaptogenesis, reducing inflammatory activation and leading to significant restoration of cognitive functions. BNN27 may represent a new lead multimodal molecule with neuroprotective, neurogenic and anti-neuroinflammatory actions for developing druggable anti-Alzheimeric agents. Proteomics data are available via ProteomeXchange with the identifier PXD044699.

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神经生长因子合成模拟物 BNN27 在 5xFAD 阿尔茨海默病小鼠模型中的多模式有益效应
阿尔茨海默病(AD)是一种无法治愈且使人衰弱的进行性神经退行性疾病,是全球痴呆症的主要病因。从神经病理学角度看,阿尔茨海默病的特征是 Aβ 淀粉样蛋白斑块在脑细胞和神经血管壁的微环境中积累、慢性神经炎症,从而导致神经元和突触丢失、髓鞘和轴突衰竭,以及成年海马神经发生显著减少。由于胆碱能回路的早期功能障碍,海马体尤其容易受到这种退化过程的影响。神经营养因子是主要的调节分子,它们在 AD 中的减少被认为是疾病发生和发展的重要原因。新的药理学方法以神经营养素控制的下游通路为靶点,如神经生长因子(NGF)受体、TrkA 和 p75NTR,可增强海马神经源能力和神经保护机制,并有可能抵消淀粉样蛋白沉积的神经毒性效应。BNN27 是一种新开发的无毒 17-螺类固醇类似物,可穿透血脑屏障(BBB),模拟 NGF 的神经保护作用,作为其受体(TrkA 和 p75NTR)的选择性激活剂,从而促进各种神经细胞类型的存活。我们目前的研究旨在确定 BNN27 是否能够缓解注意力缺失症相关病理的哪些方面,探索注意力缺失症的细胞和分子成分,并将这些变化与注意力缺失症动物模型--5xFAD 小鼠认知能力的改善联系起来。我们的研究结果清楚地表明,服用 BNN27 能显著降低动物全脑中的淀粉样蛋白-β负荷,增强成年海马的神经发生,恢复胆碱能功能和突触生成,减少炎症激活,从而显著恢复认知功能。BNN27 可能代表了一种新的多模式先导分子,具有神经保护、神经源和抗神经炎症作用,可用于开发可入药的抗阿尔茨海默病药物。蛋白质组学数据可通过 ProteomeXchange 获取,标识符为 PXD044699。
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来源期刊
Molecular Psychiatry
Molecular Psychiatry 医学-精神病学
CiteScore
20.50
自引率
4.50%
发文量
459
审稿时长
4-8 weeks
期刊介绍: Molecular Psychiatry focuses on publishing research that aims to uncover the biological mechanisms behind psychiatric disorders and their treatment. The journal emphasizes studies that bridge pre-clinical and clinical research, covering cellular, molecular, integrative, clinical, imaging, and psychopharmacology levels.
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