Superparamagnetic Iron Oxide-Enhanced Magnetic Resonance Imaging of Neuroinflammation in a Rat Model of Radicular Pain

被引:16
|
作者
Thorek, Daniel L. J. [1 ]
Weisshaar, Christine L. [1 ]
Czupryna, Julie C. [1 ]
Winkelstein, Beth A. [1 ]
Tsourkas, Andrew [1 ]
机构
[1] Univ Penn, Dept Bioengn, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
SPINAL GLIAL ACTIVATION; DORSAL-ROOT GANGLION; CYTOKINE MESSENGER-RNA; SOFT-TISSUE INFECTION; IN-VIVO; MACROPHAGE INFILTRATION; ASYMPTOMATIC SUBJECTS; NEUROPATHIC PAIN; NERVE INJURY; CERVICAL RADICULOPATHY;
D O I
10.2310/7290.2010.00042
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In many clinical cases of radicular pain, no noticeable neuropathology is detected by conventional medical imaging strategies. Superparamagnetic iron oxide (SPIO) nanoparticles were evaluated as magnetic resonance contrast agents to specifically detect neuroinflammation at sites of painful injury in a rat model of cervical nerve root compression. Two separate groups of rats were used: an injury group that underwent controlled transient compression of the dorsal root and a sham group that received the same surgical procedures but no injury. Precontrast magnetic resonance imaging (MRI) was performed 6 days after surgery, followed by administration of SPIO via tail vein injection. After 24 hours, T(2)*-weighted imaging at the site of root injury revealed a postcontrast enhancement of 72.9 +/- 3 1%. This was significantly greater than that of injured animals prior to SPIO administration (5.3 +/- 12.9%). SPIO did not generate any significant postcontrast enhancement in the nerve roots of the sham group. Histology confirmed colocalization of SPIO with macrophage at the injury site. These findings suggest that SPIO-enhanced MRI may be a valuable tool to identify otherwise undetectable nerve root compression and enable improved patient management.
引用
收藏
页码:206 / 214
页数:9
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