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脊椎动物神经系统中髓鞘变化的体内定量分析。

In vivo quantification of myelin changes in the vertebrate nervous system.

作者信息

Wang Yanming, Wu Chunying, Caprariello Andrew V, Somoza Eduardo, Zhu Wenxia, Wang Changning, Miller Robert H

机构信息

Division of Radiopharmaceutical Science, Case Center for Imaging Research, Department of Radiology, and Department of Neurosciences, Case Western Reserve University, Cleveland, Ohio 44106, USA.

出版信息

J Neurosci. 2009 Nov 18;29(46):14663-9. doi: 10.1523/JNEUROSCI.4082-08.2009.

DOI:10.1523/JNEUROSCI.4082-08.2009
PMID:19923299
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2896044/
Abstract

Destruction or changes associated with myelin membranes in the CNS play a key role in the pathogenesis of multiple sclerosis and other related neurodegenerative disorders. A long-standing goal has been to detect and quantify myelin content in vivo. For this reason, we have developed a myelin-imaging technique based on positron emission tomography (PET). PET is a quantitative imaging modality that has been widely used in clinical settings for direct assessment of biological processes at the molecular level. However, lack of myelin-imaging probes has hampered the use of PET for imaging of myelination in the CNS. Here, we report a myelin-imaging agent, termed Case Imaging Compound (CIC) that readily penetrates the blood-brain barrier and preferentially localizes to myelinated regions of the brain. After radiolabeling with positron-emitting carbon-11, [(11)C]CIC-PET was conducted in longitudinal studies using a lysolethicin-induced rat model of focal demyelination and subsequent remyelination. Quantitative analysis showed that the retention of [(11)C]CIC correlates with the level of demyelination/remyelination. These studies indicate that, for the first time, [(11)C]CIC-PET can be used as an imaging marker of myelination, which has the potential to be translated into clinical studies in multiple sclerosis and other myelin-related diseases for early diagnosis, subtyping, and efficacy evaluation of therapeutic treatments aimed at myelin repair.

摘要

中枢神经系统中与髓鞘膜相关的破坏或变化在多发性硬化症和其他相关神经退行性疾病的发病机制中起关键作用。长期以来的目标是在体内检测和量化髓鞘含量。因此,我们开发了一种基于正电子发射断层扫描(PET)的髓鞘成像技术。PET是一种定量成像方式,已在临床环境中广泛用于在分子水平直接评估生物过程。然而,缺乏髓鞘成像探针阻碍了PET用于中枢神经系统髓鞘形成的成像。在此,我们报告一种髓鞘成像剂,称为病例成像化合物(CIC),它能轻易穿透血脑屏障并优先定位于脑的髓鞘化区域。用发射正电子的碳-11进行放射性标记后,[(11)C]CIC-PET在使用溶血卵磷脂诱导的局灶性脱髓鞘和随后再髓鞘化的大鼠模型的纵向研究中进行。定量分析表明,[(11)C]CIC的滞留与脱髓鞘/再髓鞘化水平相关。这些研究表明,[(11)C]CIC-PET首次可作为髓鞘形成的成像标志物,有可能转化为多发性硬化症和其他髓鞘相关疾病的临床研究,用于早期诊断、分型以及针对髓鞘修复的治疗疗效评估。

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