IMAGING NERVES IN PAIN High-resolution magnetic resonance neurography provides excellent visualization of peripheral nerves and may be an integral component in evaluating nerve injuries, supplementing electrodiagnostic (ED) studies, such as electromyography, nerve conduction studies, and quantitative neurosensory testing.40 Structural imaging of nerve bundles, however, has Inhibitors,research,lifescience,medical been optimized to provide 3-dimensional high-resolution and high-contrast neurography. Diffusion-weighted magnetic resonance imaging (DWI) demonstrates the random diffusion of water. By evaluating water diffusion in multiple

directions, nerve fiber tracts, with their myelin sheath, may be visualized though tractography, as water diffuses Inhibitors,research,lifescience,medical along but not across the nerve bundles.41 Functional imaging of the nerves and nerve roots has, to the best of our knowledge, not yet been achieved. The utility of structural and diffusion imaging

of neuropathies is illustrated by a collection of prominent studies,42–45 reproduced in Figure 2. Figure 2 Examples Inhibitors,research,lifescience,medical of MRI Nerve Imaging. IMAGING NERVE ROOTS IN PAIN Primary afferent nerves in the GW9662 price dorsal root ganglia convey pain information to the central nervous system. Both peripheral inflammation and nerve damage can lead to alterations in anatomy and function of neurons within the ganglion, alterations that contribute to persistent pain states.46,47 While the dorsal roots are too small for standard neuroimaging approaches, the trigeminal ganglion serves an equivalent role for the trigeminal nerve. The trigeminal ganglion is located at the base of the brain in the posterior cranial

fossa across the superior border of the petrous temporal bone. It comprises Inhibitors,research,lifescience,medical Inhibitors,research,lifescience,medical sensory neurons from the ophthalmic (V1), maxillary (V2), and mandibular (V3) divisions of the trigeminal nerve. We have demonstrated that fMRI can be used to assess both sensory (brush) and noxious thermal activation of the ganglion. Activation occurred ipsilaterally and somatotopically, as predicted by the known anatomical segregation of the neurons comprising the V1, V2, and V3 divisions of the nerve (Figure 3).46 We have further demonstrated that sensory processing in patients with trigeminal neuropathic pain is associated with distinct activation patterns Dichloromethane dehalogenase consistent with sensitization within and outside of the primary sensory pathway,48 and, in a case study, we demonstrated trigeminal ganglion activation in photophobia.49 Using diffusion tensor imaging, we have further been able to segment the peripheral trigeminal circuitry, trigeminal nerve branches (ophthalmic, maxillary, and mandibular nerves), ganglion, and nerve root, and further segment the spinal trigeminal and trigeminal thalamic tracts, which, respectively, convey information to the spinal trigeminal nuclei and ventral thalamic regions.