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在体大鼠海马区区域性增强递送钆标记白蛋白。

Regional convection-enhanced delivery of gadolinium-labeled albumin in the rat hippocampus in vivo.

机构信息

Department of Biomedical Engineering, University of Florida, Gainesville, FL, United States.

出版信息

J Neurosci Methods. 2010 Mar 15;187(1):129-37. doi: 10.1016/j.jneumeth.2010.01.002. Epub 2010 Jan 11.

DOI:10.1016/j.jneumeth.2010.01.002
PMID:20067808
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2938958/
Abstract

Convection-enhanced delivery (CED) has emerged as a promising method of targeted drug delivery for treating central nervous system (CNS) disorders, but the influence of brain structure on infusate distribution is unclear. We have utilized this approach to study extracellular transport and distribution of a contrast agent in the hippocampus, a complex structure susceptible to CNS disorders. The magnetic resonance (MR) contrast agent diethylene triamene penta-acetic acid chelated gadolinium-labeled albumin (Gd-albumin), tagged with Evans blue dye, was directly infused (V(i)=5 microl) into the dorsal and ventral hippocampus of seven male Sprague-Dawley rats. The final distribution profile of the contrast agent, a product of CED and limited diffusion, was observed in vivo using high-resolution T1-weighted MR imaging at 11.1T. Dense cell layers, such as the granule cell layer of the dentate gyrus and the pyramidal cell layer of CA1, appeared to be barriers to transport of the tracer. Three-dimensional distribution shape and volume (V(d)) differences, between the dorsal and ventral hippocampus infusions, were determined from the MR images using a semi-automatic segmentation routine (dorsal V(d)=23.4+/-1.8 microl, ventral V(d)=36.4+/-5.1 microl). Finer structural detail of the hippocampus was obtained using a combination of histological analysis and fluorescence imaging. This study demonstrates that CED has the potential to target all regions of the hippocampus and that tracer distribution is influenced by infusion site, underlying structure and circuitry, and extent of backflow. Therefore, CED, combined with high-resolution MR imaging, may be a useful strategy for delivering therapeutics for the treatment of CNS disorders affecting the hippocampus.

摘要

脑室内输注(CED)已成为治疗中枢神经系统(CNS)疾病的一种有前途的靶向药物递送方法,但脑结构对输注物分布的影响尚不清楚。我们利用这种方法研究了磁共振(MR)造影剂二乙烯三胺五乙酸螯合钆标记白蛋白(Gd-白蛋白)在海马体中的细胞外转运和分布情况,海马体是一种易受 CNS 疾病影响的复杂结构。带 Evans 蓝染料的 Gd-白蛋白通过 CED 直接输注(V(i)=5 微升)到 7 只雄性 Sprague-Dawley 大鼠的背侧和腹侧海马体。使用 11.1T 高分辨率 T1 加权 MR 成像,在体内观察到 CED 和扩散受限的造影剂的最终分布图谱。高密度细胞层,如齿状回颗粒细胞层和 CA1 锥体细胞层,似乎是示踪剂转运的障碍。使用半自动分割程序(背侧 V(d)=23.4+/-1.8 微升,腹侧 V(d)=36.4+/-5.1 微升)从 MR 图像确定背侧和腹侧海马体输注之间的三维分布形状和体积(V(d))差异。使用组织学分析和荧光成像的组合获得了海马体更精细的结构细节。这项研究表明,CED 有可能靶向海马体的所有区域,并且示踪剂的分布受到输注部位、基础结构和电路以及回流程度的影响。因此,CED 结合高分辨率 MR 成像可能是治疗影响海马体的 CNS 疾病的一种有用策略。

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