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This article is part of the supplement: Proceedings of the 8th Global Arthritis Research Network (GARN) Meeting and 1st Bio-Rheumatology International Congress (BRIC)

Oral presentation

Recent advances in understanding of various chronic pain mechanisms through lysophosphatidic acid (LPA) receptor signaling

Hiroshi Ueda

  • Correspondence: Hiroshi Ueda

Author affiliations

Division of Molecular Pharmacology and Neuroscience, Nagasaki University Graduate School Biomedical Sciences, Nagasaki 852-8521, Japan

Citation and License

Arthritis Research & Therapy 2012, 14(Suppl 1):O6  doi:10.1186/ar3561

The electronic version of this article is the complete one and can be found online at: http://arthritis-research.com/content/14/S1/O6


Published:9 February 2012

© 2012 Ueda; licensee BioMed Central Ltd.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Oral presentation

Lysophosphatidic acid (LPA) receptor (LPA1) signaling plays the key role in initiation of nerve injury-induced neuropathic pain [1-4]. LPA, which is produced in the spinal cord following the sciatic nerve injury causes a calpain-mediated demyelination of dorsal root fibers and sprouting through LPA1 receptor, leading to an induction of synaptic reorganization underlying allodynia. The LPA1 signaling also initiates the up-regulation of Cavα2δ1 in DRG, leading to an enhancement of spinal pain transmission underlying hyperalgesia. Similar LPA1-mediated chronic abnormal pain and underlying mechanisms are observed in mouse models with Meth-A sarcoma surrounding sciatic nerve (cancer model) or with chemotherapy (paclitaxel). Central neuropathic pain following spinal nerve injury is now recently found to include the LPA1-mediated mechanisms. In contrast, (arthritic) inflammatory pain following Complete Freund Adjuvant treatment fails to show the involvement of LPA1 signaling. Thus it seems that many models of neuropathic pain, but not inflammatory pain model include LPA1-mediated mechanisms.

Recent studies revealed that another subtype LPA3 receptor plays a crucial role in neuropathic pain mechanisms in terms of LPA biosynthesis. Nerve injury and intrathecal administration of LPA increased the levels of lysophosphatidylcholine (LPC) and LPA in the spinal dorsal horn and dorsal root with peaks at 1 - 2 h. We obtained the evidence for in vitro LPA biosynthesis in spinal dorsal horn and dorsal root as well as in vivo one. In these studies we successfully identified the species of LPC and LPA molecules by use of Mass Spectrometery. Major species are the molecules with lipid chain 16:0, 18:0 or 18:1, and their contents were all time-dependently increased by nerve injury. Interestingly, there was an LPA-induced amplification of LPA biosynthesis through an activation of LPA3 receptor and microglia. The microglial involvement was found to play key roles as an initiation of neuropathic pain mechanisms including LPA3-mediated amplification of LPA biosynthesis.

References

  1. Inoue M, Rashid MH, Fujita R, Contos JJ, Chun J, Ueda H: Initiation of neuropathic pain requires lysophosphatidic acid receptor signaling.

    Nat Med 2004, 10:712-718. PubMed Abstract | Publisher Full Text OpenURL

  2. Ueda H: Molecular mechanisms of neuropathic pain-phenotypic switch and initiation mechanisms.

    Pharmacol Ther 2006, 109:57-77.

    Review

    PubMed Abstract | Publisher Full Text OpenURL

  3. Ueda H: Peripheral mechanisms of neuropathic pain - involvement of lysophosphatidic acid receptor-mediated demyelination.

    Mol Pain 2008, 4:11.

    Review

    PubMed Abstract | BioMed Central Full Text | PubMed Central Full Text OpenURL

  4. Ueda H: Lysophosphatidic acid as the initiator of neuropathic pain.

    Biol Pharm Bull 2011, 34:1154-1158.

    Review

    PubMed Abstract | Publisher Full Text OpenURL