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脑穿透性和疾病部位靶向性二氧化锰-聚合物-脂质杂化纳米颗粒通过调节多种病理途径重塑阿尔茨海默病微环境。

Brain-Penetrating and Disease Site-Targeting Manganese Dioxide-Polymer-Lipid Hybrid Nanoparticles Remodel Microenvironment of Alzheimer's Disease by Regulating Multiple Pathological Pathways.

作者信息

Park Elliya, Li Lily Yi, He Chunsheng, Abbasi Azhar Z, Ahmed Taksim, Foltz Warren D, O'Flaherty Regan, Zain Maham, Bonin Robert P, Rauth Andrew M, Fraser Paul E, Henderson Jeffrey T, Wu Xiao Yu

机构信息

Leslie Dan Faculty of Pharmacy, University of Toronto, 144 College St, Toronto, ON, M5S 3M2, Canada.

Department of Radiation Oncology, University Health Network, 149 College St, Toronto, ON, M5T 1P5, Canada.

出版信息

Adv Sci (Weinh). 2023 Apr;10(12):e2207238. doi: 10.1002/advs.202207238. Epub 2023 Feb 19.

Abstract

Finding effective disease-modifying treatment for Alzheimer's disease remains challenging due to an array of factors contributing to the loss of neural function. The current study demonstrates a new strategy, using multitargeted bioactive nanoparticles to modify the brain microenvironment to achieve therapeutic benefits in a well-characterized mouse model of Alzheimer's disease. The application of brain-penetrating manganese dioxide nanoparticles significantly reduces hypoxia, neuroinflammation, and oxidative stress; ultimately reducing levels of amyloid β plaques within the neocortex. Analyses of molecular biomarkers and magnetic resonance imaging-based functional studies indicate that these effects improve microvessel integrity, cerebral blood flow, and cerebral lymphatic clearance of amyloid β. These changes collectively shift the brain microenvironment toward conditions more favorable to continued neural function as demonstrated by improved cognitive function following treatment. Such multimodal disease-modifying treatment may bridge critical gaps in the therapeutic treatment of neurodegenerative disease.

摘要

由于一系列导致神经功能丧失的因素,寻找治疗阿尔茨海默病的有效疾病修饰疗法仍然具有挑战性。当前的研究展示了一种新策略,即使用多靶点生物活性纳米颗粒来改变大脑微环境,从而在一个特征明确的阿尔茨海默病小鼠模型中实现治疗效果。穿透大脑的二氧化锰纳米颗粒的应用显著降低了缺氧、神经炎症和氧化应激;最终降低了新皮质内β淀粉样蛋白斑的水平。分子生物标志物分析和基于磁共振成像的功能研究表明,这些作用改善了微血管完整性、脑血流量以及β淀粉样蛋白的脑淋巴清除率。这些变化共同将大脑微环境转变为更有利于持续神经功能的状态,治疗后认知功能的改善就证明了这一点。这种多模式疾病修饰疗法可能填补神经退行性疾病治疗中的关键空白。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76c0/10131868/681f8e65ea7d/ADVS-10-2207238-g005.jpg

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