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超声增强分子成像和治疗剂在阿尔茨海默病小鼠模型中的递送

Ultrasound enhanced delivery of molecular imaging and therapeutic agents in Alzheimer's disease mouse models.

作者信息

Raymond Scott B, Treat Lisa H, Dewey Jonathan D, McDannold Nathan J, Hynynen Kullervo, Bacskai Brian J

机构信息

The Harvard-MIT Division of Health Sciences and Technology, Cambridge, Massachusetts, United States of America.

出版信息

PLoS One. 2008 May 14;3(5):e2175. doi: 10.1371/journal.pone.0002175.

Abstract

Alzheimer's disease is a neurodegenerative disorder typified by the accumulation of a small protein, beta-amyloid, which aggregates and is the primary component of amyloid plaques. Many new therapeutic and diagnostic agents for reducing amyloid plaques have limited efficacy in vivo because of poor transport across the blood-brain barrier. Here we demonstrate that low-intensity focused ultrasound with a microbubble contrast agent may be used to transiently disrupt the blood-brain barrier, allowing non-invasive, localized delivery of imaging fluorophores and immunotherapeutics directly to amyloid plaques. We administered intravenous Trypan blue, an amyloid staining red fluorophore, and anti-amyloid antibodies, concurrently with focused ultrasound therapy in plaque-bearing, transgenic mouse models of Alzheimer's disease with amyloid pathology. MRI guidance permitted selective treatment and monitoring of plaque-heavy anatomical regions, such as the hippocampus. Treated brain regions exhibited 16.5+/-5.4-fold increase in Trypan blue fluorescence and 2.7+/-1.2-fold increase in anti-amyloid antibodies that localized to amyloid plaques. Ultrasound-enhanced delivery was consistently reproduced in two different transgenic strains (APPswe:PSEN1dE9, PDAPP), across a large age range (9-26 months), with and without MR guidance, and with little or no tissue damage. Ultrasound-mediated, transient blood-brain barrier disruption allows the delivery of both therapeutic and molecular imaging agents in Alzheimer's mouse models, which should aid pre-clinical drug screening and imaging probe development. Furthermore, this technique may be used to deliver a wide variety of small and large molecules to the brain for imaging and therapy in other neurodegenerative diseases.

摘要

阿尔茨海默病是一种神经退行性疾病,其典型特征是一种小蛋白质β-淀粉样蛋白的积累,该蛋白聚集并成为淀粉样斑块的主要成分。由于难以穿过血脑屏障,许多用于减少淀粉样斑块的新型治疗和诊断药物在体内的疗效有限。在此,我们证明,低强度聚焦超声联合微泡造影剂可用于短暂破坏血脑屏障,从而实现将成像荧光团和免疫治疗药物直接无创、局部地递送至淀粉样斑块。在患有淀粉样病变的阿尔茨海默病转基因小鼠模型中,我们在进行聚焦超声治疗的同时静脉注射台盼蓝(一种淀粉样染色红色荧光团)和抗淀粉样抗体。磁共振成像(MRI)引导允许对诸如海马体等富含斑块的解剖区域进行选择性治疗和监测。经治疗的脑区中,台盼蓝荧光增加了16.5±5.4倍,定位于淀粉样斑块的抗淀粉样抗体增加了2.7±1.2倍。在两种不同的转基因品系(APPswe:PSEN1dE9、PDAPP)中,在较大年龄范围(9 - 26个月)内,无论有无MRI引导,均能持续再现超声增强递送效果,且几乎没有组织损伤。超声介导的短暂血脑屏障破坏能够在阿尔茨海默病小鼠模型中递送治疗药物和分子成像剂,这将有助于临床前药物筛选和成像探针开发。此外,该技术可用于向大脑递送各种大小分子,以用于其他神经退行性疾病的成像和治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e352/2364662/c078712f1c1c/pone.0002175.g001.jpg

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