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Noxious stimulation induces Trk receptor and downstream ERK phosphorylation in spinal dorsal horn


Reference:

Pezet, S., Malcangio, M., Lever, I. J., Perkinton, M. S., Thompson, S. W. N., Williams, R. J. and McMahon, S. B., 2002. Noxious stimulation induces Trk receptor and downstream ERK phosphorylation in spinal dorsal horn. Molecular and Cellular Neuroscience, 21 (4), pp. 684-95.

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Official URL:

http://dx.doi.org/10.1006/mcne.2002.1205

Abstract

Several lines of evidence suggest that the brain-derived neurotrophic factor (BDNF) acts as central pain neuromodulator. We examined the ability of different types of peripheral stimulation to activate the BDNF high-affinity receptor, TrkB, in the spinal cord. We found that noxious chemical, mechanical, or thermal stimuli, but not innocuous stimuli, caused Trk phosphorylation in the spinal cord. These changes were rapid and transient and restricted to somatotopically appropriate spinal segments. We observed, both in vitro and in vivo, that exogenous BDNF induced a rapid activation of ERK, a signaling kinase important in the development of acute pain. Finally, we found that sequestering BDNF in vivo with a TrkB-IgG fusion molecule significantly reduced the activation of ERK evoked by noxious stimulation. These data suggest that BDNF, once released with activity from primary afferent nociceptors, exerts a neuromodulatory role in pain processing through stimulation of postsynaptic TrkB receptors and subsequent activation of ERK.

Details

Item Type Articles
CreatorsPezet, S., Malcangio, M., Lever, I. J., Perkinton, M. S., Thompson, S. W. N., Williams, R. J. and McMahon, S. B.
DOI10.1006/mcne.2002.1205
DepartmentsFaculty of Science > Biology & Biochemistry
RefereedYes
StatusPublished
ID Code30545

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