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扫描超声清除淀粉样蛋白-β并恢复阿尔茨海默病小鼠模型的记忆。

Scanning ultrasound removes amyloid-β and restores memory in an Alzheimer's disease mouse model.

机构信息

Clem Jones Centre for Ageing Dementia Research, Queensland Brain Institute, The University of Queensland, St Lucia Campus, Brisbane, Queensland 4072, Australia.

出版信息

Sci Transl Med. 2015 Mar 11;7(278):278ra33. doi: 10.1126/scitranslmed.aaa2512.

Abstract

Amyloid-β (Aβ) peptide has been implicated in the pathogenesis of Alzheimer's disease (AD). We present a nonpharmacological approach for removing Aβ and restoring memory function in a mouse model of AD in which Aβ is deposited in the brain. We used repeated scanning ultrasound (SUS) treatments of the mouse brain to remove Aβ, without the need for any additional therapeutic agent such as anti-Aβ antibody. Spinning disk confocal microscopy and high-resolution three-dimensional reconstruction revealed extensive internalization of Aβ into the lysosomes of activated microglia in mouse brains subjected to SUS, with no concomitant increase observed in the number of microglia. Plaque burden was reduced in SUS-treated AD mice compared to sham-treated animals, and cleared plaques were observed in 75% of SUS-treated mice. Treated AD mice also displayed improved performance on three memory tasks: the Y-maze, the novel object recognition test, and the active place avoidance task. Our findings suggest that repeated SUS is useful for removing Aβ in the mouse brain without causing overt damage, and should be explored further as a noninvasive method with therapeutic potential in AD.

摘要

淀粉样蛋白-β(Aβ)肽与阿尔茨海默病(AD)的发病机制有关。我们提出了一种非药物方法,用于去除 Aβ 并恢复 AD 小鼠模型中的记忆功能,其中 Aβ 在大脑中沉积。我们使用重复的扫描超声(SUS)治疗小鼠大脑以去除 Aβ,而无需任何其他治疗剂,如抗 Aβ 抗体。旋转盘共聚焦显微镜和高分辨率三维重建显示,SUS 处理后的小鼠大脑中的 Aβ 被大量内化到活化的小胶质细胞的溶酶体中,而小胶质细胞的数量没有观察到相应增加。与假处理动物相比,SUS 处理的 AD 小鼠的斑块负担减少,并且在 75%的 SUS 处理的小鼠中观察到清除的斑块。经治疗的 AD 小鼠在三个记忆任务中的表现也得到了改善:Y 迷宫、新物体识别测试和主动回避任务。我们的研究结果表明,重复的 SUS 有助于去除小鼠大脑中的 Aβ,而不会造成明显的损伤,并且应该作为一种具有治疗潜力的非侵入性方法在 AD 中进一步探索。

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