Evidence for biological effects of exogenous LPA on rat primary afferent and spinal cord neurons - PubMed (original) (raw)
Comparative Study
Evidence for biological effects of exogenous LPA on rat primary afferent and spinal cord neurons
Steven J R Elmes et al. Brain Res. 2004.
Abstract
There is growing behavioural evidence that the phospholipid growth factor lysophosphatidic acid (LPA) modulates nociceptive responses in vivo. The present study investigated further the effects of LPA on peripheral nociceptive processing. Effects of intraplantar injection of LPA on ongoing and peripheral mechanically evoked responses of spinal neurons were studied in vivo. In addition, LPA-evoked responses of adult rat dorsal root ganglion (DRG) neurons were studied with calcium imaging. To determine whether LPA may also act at the level of the spinal cord, LPA receptor G-protein coupling in lumbar spinal cord sections was studied with in vitro autoradiography of guanylyl 5'-[g-[(35)S]thio]triphosphate ([(35)S]GTPgammaS) binding. Intraplantar injection of LPA (5 microg/5 microl) significantly increased the duration (P<0.001) and frequency of spinal neuronal firing (P<0.01), compared to vehicle. Intraplantar injection of LPA (1 microg/5 microl) did not significantly alter innocuous and noxious mechanically evoked responses of spinal neurons, but a higher dose of LPA (5 microg) significantly (P<0.05) attenuated mechanically evoked responses of spinal neurons. Calcium imaging studies demonstrated that LPA (0.001-3 microM) increases intracellular calcium concentration in adult DRG neurons, suggesting that LPA can produce direct effects on. Incubation of spinal cord sections with LPA (1 microM) significantly (P<0.001) increased [(35)S]GTPgammaS binding in the superficial laminae of the dorsal horn of the spinal cord, suggesting that LPA may also have biological effects at this level. These data provide further evidence that exogenous LPA can modulate nociceptive processing and suggest that this may be mediated by a direct effect on primary afferent nociceptors.
Similar articles
- Loss of TRPV1-expressing sensory neurons reduces spinal mu opioid receptors but paradoxically potentiates opioid analgesia.
Chen SR, Pan HL. Chen SR, et al. J Neurophysiol. 2006 May;95(5):3086-96. doi: 10.1152/jn.01343.2005. Epub 2006 Feb 8. J Neurophysiol. 2006. PMID: 16467418 - TRPV1 and CB(1) receptor-mediated effects of the endovanilloid/endocannabinoid N-arachidonoyl-dopamine on primary afferent fibre and spinal cord neuronal responses in the rat.
Sagar DR, Smith PA, Millns PJ, Smart D, Kendall DA, Chapman V. Sagar DR, et al. Eur J Neurosci. 2004 Jul;20(1):175-84. doi: 10.1111/j.1460-9568.2004.03481.x. Eur J Neurosci. 2004. PMID: 15245490 - Inflammation enhances Y1 receptor signaling, neuropeptide Y-mediated inhibition of hyperalgesia, and substance P release from primary afferent neurons.
Taylor BK, Fu W, Kuphal KE, Stiller CO, Winter MK, Chen W, Corder GF, Urban JH, McCarson KE, Marvizon JC. Taylor BK, et al. Neuroscience. 2014 Jan 3;256:178-94. doi: 10.1016/j.neuroscience.2013.10.054. Epub 2013 Oct 31. Neuroscience. 2014. PMID: 24184981 Free PMC article. - Lysophosphatidic acid: chemical signature of neuropathic pain.
Ueda H, Matsunaga H, Olaposi OI, Nagai J. Ueda H, et al. Biochim Biophys Acta. 2013 Jan;1831(1):61-73. doi: 10.1016/j.bbalip.2012.08.014. Epub 2012 Aug 29. Biochim Biophys Acta. 2013. PMID: 22960381 Review. - Investigation of Pain Mechanisms by Calcium Imaging Approaches.
Anderson M, Zheng Q, Dong X. Anderson M, et al. Neurosci Bull. 2018 Feb;34(1):194-199. doi: 10.1007/s12264-017-0139-9. Epub 2017 May 13. Neurosci Bull. 2018. PMID: 28501905 Free PMC article. Review.
Cited by
- Mechanism and role of the intra-axonal Calreticulin translation in response to axonal injury.
Pacheco A, Merianda TT, Twiss JL, Gallo G. Pacheco A, et al. Exp Neurol. 2020 Jan;323:113072. doi: 10.1016/j.expneurol.2019.113072. Epub 2019 Oct 25. Exp Neurol. 2020. PMID: 31669485 Free PMC article. - Lysophospholipids and Their G-Coupled Protein Signaling in Alzheimer's Disease: From Physiological Performance to Pathological Impairment.
Hao Y, Guo M, Feng Y, Dong Q, Cui M. Hao Y, et al. Front Mol Neurosci. 2020 Apr 15;13:58. doi: 10.3389/fnmol.2020.00058. eCollection 2020. Front Mol Neurosci. 2020. PMID: 32351364 Free PMC article. - Role of PAF receptor in proinflammatory cytokine expression in the dorsal root ganglion and tactile allodynia in a rodent model of neuropathic pain.
Hasegawa S, Kohro Y, Shiratori M, Ishii S, Shimizu T, Tsuda M, Inoue K. Hasegawa S, et al. PLoS One. 2010 May 3;5(5):e10467. doi: 10.1371/journal.pone.0010467. PLoS One. 2010. PMID: 20454616 Free PMC article. - Involvement of lysophosphatidic acid in bone cancer pain by potentiation of TRPV1 via PKCε pathway in dorsal root ganglion neurons.
Pan HL, Zhang YQ, Zhao ZQ. Pan HL, et al. Mol Pain. 2010 Dec 1;6:85. doi: 10.1186/1744-8069-6-85. Mol Pain. 2010. PMID: 21118579 Free PMC article. - Functional significance of M-type potassium channels in nociceptive cutaneous sensory endings.
Passmore GM, Reilly JM, Thakur M, Keasberry VN, Marsh SJ, Dickenson AH, Brown DA. Passmore GM, et al. Front Mol Neurosci. 2012 May 14;5:63. doi: 10.3389/fnmol.2012.00063. eCollection 2012. Front Mol Neurosci. 2012. PMID: 22593734 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Miscellaneous