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长期血管通路作为一种在啮齿类 fMRI 生存模型中给予镇静剂的方式。

Long-term vascular access ports as a means of sedative administration in a rodent fMRI survival model.

机构信息

Department of Plastic Surgery, 8700 Watertown Plank Road, Medical College of Wisconsin, Milwaukee, WI 53226, USA.

出版信息

J Neurosci Methods. 2011 Sep 15;200(2):106-12. doi: 10.1016/j.jneumeth.2011.06.018. Epub 2011 Jun 24.

DOI:10.1016/j.jneumeth.2011.06.018
PMID:21726581
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3156352/
Abstract

The purpose of this study is to develop a rodent functional magnetic resonance imaging (fMRI) survival model with the use of heparin-coated vascular access devices. Such a model would ease the administration of sedative agents, reduce the number of animals required in survival experiments and eliminate animal-to-animal variability seen in previous designs. Seven male Sprague-Dawley rats underwent surgical placement of an MRI-compatible vascular access port, followed by implantable electrode placement on the right median nerve. Functional MRI during nerve stimulation and resting-state functional connectivity MRI (fcMRI) were performed at times 0, 2, 4, 8 and 12 weeks postoperatively using a 9.4T scanner. Anesthesia was maintained using intravenous dexmedetomidine and reversed using atipamezole. There were no fatalities or infectious complications during this study. All vascular access ports remained patent. Blood oxygen level dependent (BOLD) activation by electrical stimulation of the median nerve using implanted electrodes was seen within the forelimb sensory region (S1FL) for all animals at all time points. The number of activated voxels decreased at time points 4 and 8 weeks, returning to a normal level at 12 weeks, which is attributed to scar tissue formation and resolution around the embedded electrode. The applications of this experiment extend far beyond the scope of peripheral nerve experimentation. These vascular access ports can be applied to any survival MRI study requiring repeated medication administration, intravenous contrast, or blood sampling.

摘要

本研究旨在开发一种使用肝素涂层血管接入装置的啮齿动物功能磁共振成像(fMRI)存活模型。这种模型将便于镇静剂的给药,减少存活实验所需的动物数量,并消除之前设计中观察到的动物间变异性。七只雄性 Sprague-Dawley 大鼠接受了 MRI 兼容血管接入端口的手术放置,随后在右侧正中神经上进行了可植入电极的放置。在手术后 0、2、4、8 和 12 周,使用 9.4T 扫描仪进行神经刺激时的功能 MRI 和静息状态功能连接 MRI(fcMRI)。使用静脉内右美托咪定维持麻醉,并使用阿替美唑逆转。在这项研究中没有发生死亡或感染并发症。所有血管接入端口均保持通畅。所有动物在所有时间点都在植入电极刺激正中神经时在前肢感觉区(S1FL)中看到了血氧水平依赖(BOLD)激活。在第 4 和 8 周时,激活的体素数量减少,在第 12 周时恢复正常水平,这归因于围绕嵌入式电极的疤痕组织形成和溶解。这项实验的应用远远超出了周围神经实验的范围。这些血管接入端口可应用于任何需要重复给药、静脉内对比剂或采血的存活 MRI 研究。

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