摘要
Activity-dependent postsynaptic receptor trafficking is critical for long-term synaptic plasticity in the brain, but it is unclear whether this mechanism actually mediates the spinal cord dorsal hom central sensitization （a specific form of synaptic plasticity） that is associated with persistent pain. Recent studies have shown that peripheral inflammation drives changes in ct-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor （AMPAR） subunit trafficking in the dorsal horn and that such changes contribute to the hypersensitivity that underlies persistent pain. Here, we review current evi- dence to illustrate how spinal cord AMPARs participate in the dorsal hom central sensitization associated with persistent pain. Understanding these mechanisms may allow the development of novel therapeutic strategies for treating persistent pain.
Activity-dependent postsynaptic receptor trafficking is critical for long-term synaptic plasticity in the brain, but it is unclear whether this mechanism actually mediates the spinal cord dorsal hom central sensitization （a specific form of synaptic plasticity） that is associated with persistent pain. Recent studies have shown that peripheral inflammation drives changes in ct-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor （AMPAR） subunit trafficking in the dorsal horn and that such changes contribute to the hypersensitivity that underlies persistent pain. Here, we review current evi- dence to illustrate how spinal cord AMPARs participate in the dorsal hom central sensitization associated with persistent pain. Understanding these mechanisms may allow the development of novel therapeutic strategies for treating persistent pain.
基金
supported by grants from the National Institutes of Health (NS058886 and NS072206)
Rita Allen Foundation
Mr. David Koch and the Patrick C. Walsh Prostate Cancer Research Fund
the Blaustein Pain Research Fund
