DOI QR코드

DOI QR Code

Sigma-1 Receptor Antagonist BD1047 Reduces Allodynia and Spinal ERK Phosphorylation Following Chronic Compression of Dorsal Root Ganglion in Rats

  • Son, Ji-Seon (Department of Anesthesiology and Pain Medicine, Institute for Medical Science, Chonbuk National University Medical School) ;
  • Kwon, Young-Bae (Department of Pharmacology, Institute for Medical Science, Chonbuk National University Medical School)
  • Received : 2010.09.01
  • Accepted : 2010.10.14
  • Published : 2010.12.31

Abstract

Many therapeutic roles have been proposed for sigma-1 receptor (Sig-1R), but the involvement of Sig-1R in neuropathic pain has currently not been well explored. The present study aimed to evaluate the anti-nociceptive effect of Sig-1R antagonist (BD1047) in a rat model of chronic compression of the dorsal root ganglion (CCD), which is a model of human foraminal stenosis and radicular pain. When stainless steel rods were inserted into the intervertebral foramen of lumbar vertebrae 4 and 5, the CCD developed reliable mechanical (from 3 day) and cold allodynia (from 1 day) as compared with the sham operation group. The spinal expressions of Sig-1R and phosphorylation of extracellular signal-regulated kinase (pERK) were significantly increased from day 3 to day 14 after CCD surgery, as is consistent with the manifestation of allodynia. The BD 1047 (10, 30, 100 mg/kg) administered on postoperative days 0~5 dose-dependently suppressed both the induction of allodynia and the elevation of the spinal pERK expression in a manner comparable with that of gabapentin (100 mg/kg). At 7 days post-CCD surgery, BD1047 (10, 30, 100 mg/kg) administration also produced anti-nociceptive effects on the mechanical and cold allodynia similar with those of gabapentin (100 mg/kg). Therefore, this data suggested that Sig-1R may play an important role in both the development and maintenance of CCD-induced neuropathy.

Keywords

References

  1. Maurire T, Su TP. The pharmacology of sigma-1 receptors. Pharmacol Ther. 2009;124:195-206. https://doi.org/10.1016/j.pharmthera.2009.07.001
  2. Cendan CM, Pujalte JM, Portillo-Salido E, Montoliu L, Baeyens JM. Formalin-induced pain is reduced in sigma(1) receptor knockout mice. Eur J Pharmacol. 2005;511:73-74. https://doi.org/10.1016/j.ejphar.2005.01.036
  3. Kim HW, Kwon YB, Roh DH, Yoon SY, Han HJ, Kim KW, Beitz AJ, Lee JR. Intrathecal treatment with sigma 1 receptor antagonists reduces formalin-induced phosphorylation of NMDA receptor subunit 1 and the second phase of formalin test in mice. Br J Pharmacol. 2006;148:490-498.
  4. Kim HW, Roh DH, Yoon SY, Seo HS, Kwon YB, Han HJ, Kim KW, Beitz AJ, Lee JH. Activation of the spinal sigma-1 receptor enhances NMDA-induced pain via PKC- and PKA-dependent phosphorylation of the NR1 subunit in mice. Br J Pharmacol. 2008;154:1125-1134. https://doi.org/10.1038/bjp.2008.159
  5. Yoon SY, Roh DH, Seo HS, Rang SY, Han HJ, Beitz AJ, Lee JH. Intrathecal injection of the neurosteroid, DHEAS, produces mechanical allodynia in mice: involvement of spinal sigma-1 and GABA receptors. Br J Pharmacol. 2009;157:666-673. https://doi.org/10.1111/j.1476-5381.2009.00197.x
  6. Kibaly C, Meyer L, Patte-Mensah C, Mensah-Nyagan AG. Biochemical and functional evidence for the control of pain mechanisms by dehydroepiandrosterone endogenously synthesized in the spinal cord. FASEB J. 2008;22:93-104. https://doi.org/10.1096/fj.07-8930com
  7. de la Puente B, Nadal X, Portillo-Salido E, Sanchez-Arroyos R, Ovalle S, Palacios G, Muro A, Romero L, Entrena JM, Baeyens JM, Lopez-Garcia JA, Maldonado R, Zamanillo D, Vela JM. Sigma-1 receptors regulate activity-induced spinal sensitization and neuropathic pain after peripheral nerve injury. Pain. 2009;145:294-303. https://doi.org/10.1016/j.pain.2009.05.013
  8. Roh DH, Kim HW, Yoon SY, Seo HS, Kwon YB, Kim KW, Han HJ, Beitz AJ, Na HS, Lee JH. Intrathecal injection of the sigma(1) receptor antagonist BD1047 blocks both mechanical allodynia and increases in spinal NR1 expression during the induction phase of rodent neuropathic pain. Anesthesiology. 2008;109:879-889. https://doi.org/10.1097/ALN.0b013e3181895a83
  9. Huang ZJ, Song XJ. Differing alterations of sodium currents in small dorsal root ganglion neurons after ganglion compression and peripheral nerve injury. Mol Pain. 2008;4:20. https://doi.org/10.1186/1744-8069-4-20
  10. Ji RR, Gereau RW 4th, Malcangio M, Strichartz GR. MAP kinase and pain. Brain Res Rev. 2009;60:135-148. https://doi.org/10.1016/j.brainresrev.2008.12.011
  11. Ma W, Quirion R. Partial sciatic nerve ligation induces increase in the phosphorylation of extracellular signal-regulated kinase (ERK) and c-Jun N-terminal kinase (JNK) in astrocytes in the lumbar spinal dorsal horn and the gracile nucleus. Pain. 2002;99:175-184. https://doi.org/10.1016/S0304-3959(02)00097-0
  12. Ma C, LaMotte RH. Multiple sites for generation of ectopic spontaneous activity in neurons of the chronically compressed dorsal root ganglion. J Neurosci. 2007;27:14059-14068. https://doi.org/10.1523/JNEUROSCI.3699-07.2007
  13. Coderre TJ, Kumar N, Lefebvre CD, Yu JS. Evidence that gabapentin reduces neuropathic pain by inhibiting the spinal release of glutamate. J Neurochem. 2005;94:1131-1139. https://doi.org/10.1111/j.1471-4159.2005.03263.x
  14. Werner MF, Kassuya CA, Ferreira J, Zampronio AR, Calixto JB, Rae GA. Peripheral kinin B(1) and B(2) receptor-operated mechanisms are implicated in neuropathic nociception induced by spinal nerve ligation in rats. Neuropharmacology. 2007;53:48-57. https://doi.org/10.1016/j.neuropharm.2007.04.013
  15. Zhuang ZY, Gerner P, Woolf CJ, Ji RR. ERK is sequentially activated in neurons, microglia, and astrocytes by spinal nerve ligation and contributes to mechanical allodynia in this neuropathic pain model. Pain. 2005;114:149-159. https://doi.org/10.1016/j.pain.2004.12.022
  16. Ma W, Quirion R. The ERK/MAPK pathway, as a target for the treatment of neuropathic pain. Expert Opin Ther Targets. 2005;9:699-713. https://doi.org/10.1517/14728222.9.4.699
  17. Dubrovsky BO. Steroids, neuroactive steroids and neuro-steroids in psychopathology. Prog Neuropsychopharmacol Biol Psychiatry. 2005;29:169-192. https://doi.org/10.1016/j.pnpbp.2004.11.001
  18. Schaeffer V, Meyer L, Patte-Mensah C, Eckert A, Mensah-Nyagan AG. Sciatic nerve injury induces apoptosis of dorsal root ganglion satellite glial cells and selectively modifies neuro-steroidogenesis in sensory neurons. Glia. 2010;58:169-180. https://doi.org/10.1002/glia.20910
  19. Roh DH, Kim HW, Yoon SY, Seo HS, Kwon YB, Kim KW, Han HJ, Beitz AJ, Lee JH. Intrathecal administration of sigma-1 receptor agonists facilitates nociception: involvement of a protein kinase C-dependent pathway. J Neurosci Res. 2008;86:3644-3654. https://doi.org/10.1002/jnr.21802

Cited by

  1. Pharmacological properties of S1RA, a new sigma-1 receptor antagonist that inhibits neuropathic pain and activity-induced spinal sensitization : Antagonism of the σ1R inhibits pain sensitization vol.166, pp.8, 2010, https://doi.org/10.1111/j.1476-5381.2012.01942.x
  2. Sigma-1 receptor expression in sensory neurons and the effect of painful peripheral nerve injury vol.9, pp.None, 2010, https://doi.org/10.1186/1744-8069-9-47
  3. Selective sigma-1 receptor antagonists for the treatment of pain vol.6, pp.10, 2010, https://doi.org/10.4155/fmc.14.54
  4. Sigma-1 receptors and animal studies centered on pain and analgesia vol.10, pp.8, 2010, https://doi.org/10.1517/17460441.2015.1051961
  5. Investigational sigma-1 receptor antagonists for the treatment of pain vol.24, pp.7, 2010, https://doi.org/10.1517/13543784.2015.1048334
  6. Repeated Sigma-1 Receptor Antagonist MR309 Administration Modulates Central Neuropathic Pain Development After Spinal Cord Injury in Mice vol.10, pp.None, 2010, https://doi.org/10.3389/fphar.2019.00222
  7. Pharmacological stimulation of sigma-1 receptor promotes activation of astrocyte via ERK1/2 and GSK3β signaling pathway vol.392, pp.7, 2010, https://doi.org/10.1007/s00210-019-01632-3
  8. Antagonism of Sigma‐1 receptor blocks heavy alcohol drinking and associated hyperalgesia in male mice vol.45, pp.7, 2021, https://doi.org/10.1111/acer.14635
  9. The Peripheral Role of CCL2 in the Anti-Nociceptive Effect of Sigma-1 Receptor Antagonist BD1047 on Inflammatory Hyperalgesia in Rats vol.22, pp.21, 2010, https://doi.org/10.3390/ijms222111730