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High Resolution Functional MRI Investigation of Cortical Plasticity Following Peripheral Nerve Injury and Repair.

机译:周围神经损伤和修复后皮质可塑性的高分辨率功能MRI研究。

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摘要

Recent clinical and laboratory studies have demonstrated that significant cortical plasticity appears following peripheral nerve injury and repair. Treatment based on cortical plasticity has been applied clinically to utilize this phenomenon and ensure the best possible outcome for these patients.;The ultimate goals of this proposal are to provide insight into the neural mechanism of cortical plasticity following peripheral nerve injury and repair, to monitor this cortical plasticity with high spatial resolution on a survival animal model, and eventually to develop a noninvasive method that can be used to guide clinical practice.;First, to better understand the neurophysiological mechanism of cortical plasticity following nerve injury and repair, high field functional MRI (fMRI) was employed to detect activation induced by direct nerve trunk electrical stimulation on the peripheral nervous system (PNS) in an animal model. Two distinct cortical plasticity patterns were demonstrated following different degrees of functional deprivation. Numerous studies have shown the critical role of cortical plasticity in the functional recovery process. Therefore, it is suggested that different degrees of functional loss caused by initial injury may lead to different types of cortical plasticity.;Second, to monitor functional recovery after peripheral nerve repair, a survival animal model was employed with simple median nerve injury and instant repair. Compared with the results of the previous non-survival animal model, the motor cortex blood oxygen level dependent (BOLD) activation disappeared during the scan. Further study may suggest that BOLD activation in the motor cortex may involve only a minimum level of consciousness. In this study, the same rats were studied over a prolonged period of time. Both fMRI and behavior tests were performed throughout the process. Significant correlations between the fMRI results and the behavior test results were found. This is the first time this relationship has been systematically studied, which would not have been possible without this new survival animal model. Using the same data set, resting state functional connectivity MRI (fcMRI) was also studied. A comparison between the nerve repair and non-repair groups yielded significant difference early in the subacute stage following initial injury. This technique could potentially be used to monitor nerve repair clinically to help patients with an extremely undesirable outcome. The entire sensory recovery process following nerve repair was also demonstrated using the fMRI technique for the first time. Meanwhile, fcMRI in the insular cortex was also investigated and remains consistent across different time points and independent from the cortical sensorimotor network. It may serve as a reliable control for any survival animal study.;Furthermore, to investigate cortical plasticity caused by PNS injury and repair and to apply the methodologies developed above, brachial plexus injury and repair in an animal model was studied. Cervical nerve root No. 7 autograph (C7 transfer) was used to repair the brachial plexus injury. By following the same rats for the entire recovery period, the process of cortical plasticity was revealed. For the first time, this process was demonstrated and studied quantitatively in great detail. Because individual rats could be followed over a long period of time, inter-subject variation was also investigated. Given the fact that the outcome of C7 transfer surgery shows great diversity clinically, this study provides a way to correlate individual surgical outcome with cortical reorganization. It also provides the basis for further intervention study to improve surgical outcome.;Finally, to maximize the detection abilities of both fMRI and fcMRI for future study, high resolution functional imaging was developed. We employed a half-k-space gradient echo (GE) sequence and pseudo-randomized digit stimulation. fMRI and fcMRI were performed at the cortical-column level. Results demonstrated fMRI BOLD activation; cortical-column activation was shown to penetrate the entire five layers of the cortex. The partial-volume effect was greatly reduced. A more accurate and localized result was demonstrated compared to results with a conventional resolution. This technique provides a solid foundation to investigate the PNS cortical-layer-specific projection of different fiber types in the future.
机译:最近的临床和实验室研究表明,在周围神经损伤和修复后,皮质可塑性显着提高。临床上已经应用基于皮质可塑性的治疗方法来利用这种现象并确保这些患者获得最佳可能的结果。该建议的最终目标是深入了解周围神经损伤和修复后皮质可塑性的神经机制,以监测在生存动物模型上具有高空间分辨率的这种皮质可塑性,并最终开发出一种可用于指导临床实践的非侵入性方法。首先,为了更好地了解神经损伤和修复后皮质可塑性的神经生理机制,高视野功能MRI(fMRI)用于检测动物模型中直接神经干电刺激周围神经系统(PNS)引起的激活。在不同程度的功能丧失后,表现出两种不同的皮质可塑性模式。大量研究表明,皮质可塑性在功能恢复过程中起着至关重要的作用。因此,建议由初始损伤引起的不同程度的功能丧失可能导致不同类型的皮质可塑性。第二,为了监测周围神经修复后的功能恢复,采用了具有简单正中神经损伤和即刻修复的存活动物模型。与以前的非存活动物模型的结果相比,运动皮层血氧水平依赖性(BOLD)激活在扫描过程中消失了。进一步的研究可能表明运动皮层中的BOLD激活可能仅涉及最低意识水平。在这项研究中,对相同的大鼠进行了长时间的研究。在整个过程中都进行了功能磁共振成像和行为测试。功能磁共振成像结果与行为测试结果之间存在显着相关性。这是第一次对这种关系进行系统的研究,如果没有这种新的生存动物模型,这是不可能的。使用相同的数据集,还研究了静息状态功能连接性MRI(fcMRI)。神经修复组和非修复组之间的比较在初始损伤后的亚急性阶段早期产生了显着差异。该技术可能会潜在地用于临床监测神经修复,以帮助患者获得极为不良的结果。首次使用功能磁共振成像技术演示了神经修复后的整个感觉恢复过程。同时,还对岛状皮层中的fcMRI进行了研究,并在不同时间点保持一致,并且独立于皮层感觉运动网络。它可作为任何存活动物研究的可靠对照。此外,研究PNS损伤和修复引起的皮层可塑性并应用以上开发的方法,在动物模型中研究臂丛神经的损伤和修复。颈神经根7号亲笔签名(C7转移)用于修复臂丛神经损伤。通过跟踪整个恢复期的同一只大鼠,揭示了皮质可塑性的过程。这是首次对这一过程进行了详细的定量证明和研究。由于可以长时间跟踪单个大鼠,因此还研究了受试者间的差异。鉴于C7转移手术的结果在临床上显示出极大的多样性,这项研究提供了一种将单个手术结果与皮层重组相关的方法。最后,为进一步提高fMRI和fcMRI的检测能力以进行进一步的研究,开发了高分辨率的功能成像技术。我们采用了半k空间梯度回波(GE)序列和伪随机数字刺激。 fMRI和fcMRI在皮质柱水平进行。结果显示fMRI BOLD激活;皮质柱激活被证明穿透了皮质的整个五层。局部体积效应大大降低。与具有常规分辨率的结果相比,显示出了更加准确和本地化的结果。该技术为将来研究不同纤维类型的PNS皮层特定投影提供了坚实的基础。

著录项

  • 作者

    Li, Rupeng.;

  • 作者单位

    The Medical College of Wisconsin.;

  • 授予单位 The Medical College of Wisconsin.;
  • 学科 Health Sciences Medicine and Surgery.;Biophysics Medical.;Biophysics General.
  • 学位 Ph.D.
  • 年度 2011
  • 页码 246 p.
  • 总页数 246
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 高分子化学(高聚物);
  • 关键词

  • 入库时间 2022-08-17 11:44:18

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