The development and modulation of nociceptive circuitry
- PMID: 16828278
- DOI: 10.1016/j.conb.2006.06.002
The development and modulation of nociceptive circuitry
Abstract
Nociceptive circuitry processes the signals evoked by activating specialized peripheral sensory receptors for pain perception. Recent studies show that the neuronal phenotypes in the dorsal root ganglia and spinal dorsal horn are determined by distinct sets of transcription factors during development. Anatomical analyses with genetic approaches demonstrate that each subset of nociceptive sensory neurons has topographically distinct circuits at both spinal and brain levels. Moreover, the sensitivity of primary afferents can be rapidly regulated not only by phosphorylation of receptors, ion channels and associated regulatory proteins but also by stimulus-induced cell surface expression of G-protein-coupled receptors. In chronic pain states the molecular characteristics of spinal nociceptive circuits are altered, enabling normal peripheral stimuli to induce pain hypersensitivity.
Similar articles
-
Hyperpolarization-activated and cyclic nucleotide-gated cation channel subunit 2 ion channels modulate synaptic transmission from nociceptive primary afferents containing substance P to secondary sensory neurons in laminae I-IIo of the rodent spinal dorsal horn.Eur J Neurosci. 2006 Sep;24(5):1341-52. doi: 10.1111/j.1460-9568.2006.05013.x. Eur J Neurosci. 2006. PMID: 16987220
-
Spinal dorsal horn neurone targets for nociceptive primary afferents: do single neurone morphological characteristics suggest how nociceptive information is processed at the spinal level.Brain Res Brain Res Rev. 2004 Oct;46(2):173-90. doi: 10.1016/j.brainresrev.2004.07.002. Brain Res Brain Res Rev. 2004. PMID: 15464206 Review.
-
Synaptic modulation in pain pathways.Rev Physiol Biochem Pharmacol. 2005;154:73-100. doi: 10.1007/s10254-005-0043-y. Rev Physiol Biochem Pharmacol. 2005. PMID: 16059718 Review.
-
Runx1 determines nociceptive sensory neuron phenotype and is required for thermal and neuropathic pain.Neuron. 2006 Feb 2;49(3):365-77. doi: 10.1016/j.neuron.2005.10.036. Neuron. 2006. PMID: 16446141
-
Sex differences in the responses of spinal wide-dynamic range neurons to subcutaneous formalin and in the effects of different frequencies of conditioning electrical stimulation.Neuroscience. 2006;138(4):1299-307. doi: 10.1016/j.neuroscience.2005.11.060. Epub 2006 Jan 19. Neuroscience. 2006. PMID: 16426769
Cited by
-
Increases in mRNA and DREAM protein expression in the rat spinal cord after formalin induced pain.Neurochem Res. 2011 Mar;36(3):533-9. doi: 10.1007/s11064-010-0375-0. Epub 2010 Dec 25. Neurochem Res. 2011. PMID: 21188515
-
An in vitro assay system for studying synapse formation between nociceptive dorsal root ganglion and dorsal horn neurons.J Neurosci Methods. 2010 Jun 15;189(2):197-204. doi: 10.1016/j.jneumeth.2010.04.002. Epub 2010 Apr 10. J Neurosci Methods. 2010. PMID: 20385165 Free PMC article.
-
Towards an Effective and Safe Treatment of Inflammatory Pain: A Delphi-Guided Expert Consensus.Adv Ther. 2019 Oct;36(10):2618-2637. doi: 10.1007/s12325-019-01053-x. Epub 2019 Aug 16. Adv Ther. 2019. PMID: 31485978 Free PMC article.
-
Synaptic connections of the neurokinin 1 receptor-like immunoreactive neurons in the rat medullary dorsal horn.PLoS One. 2011;6(8):e23275. doi: 10.1371/journal.pone.0023275. Epub 2011 Aug 17. PLoS One. 2011. PMID: 21858052 Free PMC article.
-
Brn3a regulates neuronal subtype specification in the trigeminal ganglion by promoting Runx expression during sensory differentiation.Neural Dev. 2010 Jan 22;5:3. doi: 10.1186/1749-8104-5-3. Neural Dev. 2010. PMID: 20096094 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical