Diffusion tensor imaging of the injured spinal cord

受损脊髓的弥散张量成像

• 批准号: 8668988
• 负责人: Shekar N. Kurpad
• 金额: --
• 依托单位: CLEMENT J. ZABLOCKI VA MEDICAL CENTER
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-10-01 至 2012-09-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8668988
• 关键词: Animals; Behavioral; Caring; Cell physiology; Cells; Cervical; Chest; Chronic; Clinical Research; Contusions; Data; Development; Diagnostic; Diagnostic tests; Diffusion; Diffusion Magnetic Resonance Imaging; Distant; Dorsal; Effectiveness; Engineering; Evoked Potentials; Family; Fiber; Flexor; Forelimb; Future; Goals; Healthcare; Hindlimb; Histologic; Histology; Human; Image; Image Analysis; Imaging Techniques; Implant; Injury; Intervention; Joints; Length; Lesion; Location; Magnetic Resonance Imaging; Manuscripts; Measurement; Measures; Mentorship; Military Personnel; Modeling; Monitor; Morphology; Motor Evoked Potentials; Natural regeneration; Nature; Neurons; Pain; Pathology; Patients; Pattern; Permeability; Persons; Physical therapy; Pilot Projects; Population; Postdoctoral Fellow; Process; Program Reviews; Property; Publications; Rattus; Recovery; Reflex action; Rehabilitation therapy; Research; Research Support; Resolution; Scanning; Sensorimotor functions; Services; Severities; Site; Somatosensory Evoked Potentials; Spinal; Spinal Cord; Spinal cord injury; Stem cells; Structure; Testing; Thoracic spinal cord structure; Time; Tissues; Translating; Transplantation; United States; Validation; Veterans; Work; allodynia; base; clinical care; dorsal horn; experience; functional status; graduate student; gray matter; in vivo; injured; interest; meetings; morphometry; non-invasive imaging; novel; prognostic; regenerative; regenerative therapy; research and development; research study; response; sciatic nerve; spinal tract; tool

DESCRIPTION (provided by applicant): ABSTRACT Hypothesis: We hypothesize the diffusion properties and microstructure change across the entire length of the spinal cord during recovery from SCI. Also, we postulate that diffusion measurements and tissue sparing can be used to estimate sensorimotor function. In addition, we hypothesize that DTI is sensitive to regenerative interventions. Preliminary Data: Pilot studies have demonstrated the feasibility of obtaining DTI images of the injured and non-injured rat spinal cord using a high field (9.4T) small animal magnet. DTI images appear to follow expected patterns predicted by images obtained in chronic human SCI, with changes in diffusivity both at the injury site and in regions distant from the injury. Of particular note, reductions in diffusion appear in regions o fthe spinal cord distant from the injury site that correlate with histological data indicating cellular responses in neurons ofthe corresponding gray matter. Further, pilot data indicate that diffusion patterns are related to functional connectivity of the spinal cord, evidenced by correlations with spinal somatosensory evoked potentials (SSEPs). In separate studies, we have also demonstrated specific structural changes in the cervical dorsal hom of the rat spinal cord subjected to thoracic contusion injury and treated with stem cell grafts. These structural changes correlated with increased proliferation of pain fibers, which functionally resulted in the development of forelimb allodynia. We propose using this treatment paradigm, with well documented structural and functional changes, to test the diagnostic and prognostic abilities of DTI. Research Objectives: The overall goal of this project is to determine whether DTI can provide a non invasive imaging correlate of spinal cord structure and function following injury and regenerative therapies in a rat model of SCI. We plan to pursue this goal through three specific objectives. (1) Characterize region-specific changes in diffusivity during recovery from SCI. (2) Characterize functional correlates to DTI in the spinal cord during recovery from SCI. (3) Determine the sensitivity ofDTI to neuronal stem cell treatments following SCI. Our approach will use in vivo and ex vivo OTI to detemi.ine histological correlates during recovery from SCI. We will then determine the behavioral and electrophysiological functional correlates to DTI to histology and axonal morphometry. Lastly, we will determine the sensitivity of DTI to regeneration interventions with known changes in structure and function. The translational nature of this project is reflected by direct future application in humans if DTI is found to be able to detect histologically verifiable changes in morphology in the injured spinal cord.

描述（由申请人提供）： 抽象假设：我们假设脊髓损伤恢复过程中，整个脊髓的扩散特性和微观结构发生了变化。此外，我们假设扩散测量和组织保留可以用来估计感觉运动功能。此外，我们假设DTI对再生干预敏感。初步数据：初步研究已经证明了使用高场（9.4T）小动物磁体获得损伤和未损伤大鼠脊髓的DTI图像的可行性。DTI图像似乎遵循在慢性人类SCI中获得的图像预测的预期模式，在损伤部位和远离损伤的区域中的扩散率都发生变化。特别值得注意的是，扩散减少出现在脊髓远离损伤部位的区域，这与组织学数据相关，表明相应灰质神经元的细胞反应。此外，试点数据表明，扩散模式与脊髓的功能连接，证明了与脊髓体感诱发电位（SSEP）的相关性。在单独的研究中，我们也证明了特定的结构变化，在大鼠脊髓颈后角受到胸部挫伤和干细胞移植治疗。这些结构变化与疼痛纤维的增殖增加相关，这在功能上导致前肢异常性疼痛的发展。我们建议使用这种治疗模式，与有据可查的结构和功能的变化，以测试的诊断和预后能力的DTI。研究目的：本项目的总体目标是确定DTI是否可以在大鼠SCI模型中提供损伤和再生治疗后脊髓结构和功能的非侵入性成像相关性。我们计划通过三个具体目标来实现这一目标。(1)表征SCI恢复期间扩散率的区域特定变化。(2)描述SCI恢复期间脊髓中与DTI相关的功能。(3)确定SCI后DTI对神经干细胞治疗的敏感性。我们的方法将使用体内和离体OTI来确定SCI恢复过程中的组织学相关性。然后，我们将确定行为和电生理功能相关的DTI组织学和轴突形态。最后，我们将确定DTI对已知结构和功能变化的再生干预的敏感性。如果发现DTI能够检测到损伤脊髓形态学的组织学可证实的变化，则该项目的翻译性质将通过未来在人类中的直接应用而得到反映。