HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Spinal ephrinB/EphB signalling contributed to remifentanil-induced hyperalgesia via NMDA receptor.

AbstractBACKGROUND:
One of the major unresolved issues in treating pain is the paradoxical hyperalgesia produced by opiates, and accumulating evidence implicate that EphBs receptors and ephrinBs ligands are involved in mediation of spinal nociceptive information and central sensitization, but the manner in which ephrinB/EphB signalling acts on spinal nociceptive information networks to produce hyperalgesia remains enigmatic. The objective of this research was to investigate the role of ephrinB/EphB signalling in remifentanil-induced hyperalgesia (RIH) and its downstream effector.
METHODS:
We characterized the remifentanil-induced pain behaviours by evaluating thermal hyperalgesia and mechanical allodynia in a rat hind paw incisional model. Protein expression of EphB1 receptor and ephrinB1 ligand in spinal dorsal horn cord was determined by Western blotting, and Fos was determined by immunohistochemistry assay, respectively. To figure out the manner in which ephrinB/EphB signalling acts with N-methyl-d-aspartic acid (NMDA) receptor, we used MK-801, an antagonist of NMDA receptor, trying to suppressed the hyperalgesia induced by ephrinB1-Fc, an agonist of ephrinB/EphB.
RESULTS:
Continuing infusion of remifentanil produced a thermal hyperalgesia and mechanical allodynia, which was accompanied with increased protein expression of spinal-level EphB1 receptor, ephrinB1 ligand and Fos; what appeared above was suppressed by pretreatment with EphB1-Fc, an antagonist of ephrinB/EphB or MK-801, and increased pain behaviours induced by intrathecal injection of ephrinB1-Fc, an agonist of ephrinB/EphB, were suppressed by MK-801.
CONCLUSIONS:
Our findings indicated that ephrinB/EphB signalling is involved in RIH. EphrinB/EphB signalling might be the upstream of NMDA receptor.
AuthorsW S Xia, Y N Peng, L H Tang, L S Jiang, L N Yu, X L Zhou, F J Zhang, M Yan
JournalEuropean journal of pain (London, England) (Eur J Pain) Vol. 18 Issue 9 Pg. 1231-9 (Oct 2014) ISSN: 1532-2149 [Electronic] England
PMID24737575 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Copyright© 2014 The Authors. European Journal of Pain published by John Wiley & Sons Ltd on behalf of European Pain Federation - EFIC®.
Chemical References
  • Analgesics, Opioid
  • Ephrin-B1
  • Excitatory Amino Acid Antagonists
  • Piperidines
  • Receptors, N-Methyl-D-Aspartate
  • Dizocilpine Maleate
  • Receptor, EphB1
  • Remifentanil
Topics
  • Analgesics, Opioid (adverse effects, pharmacology)
  • Animals
  • Disease Models, Animal
  • Dizocilpine Maleate (pharmacology)
  • Ephrin-B1 (agonists, antagonists & inhibitors, metabolism)
  • Excitatory Amino Acid Antagonists (pharmacology)
  • Hyperalgesia (chemically induced)
  • Male
  • Piperidines (adverse effects, pharmacology)
  • Rats
  • Rats, Sprague-Dawley
  • Receptor, EphB1 (agonists, antagonists & inhibitors, metabolism)
  • Receptors, N-Methyl-D-Aspartate (antagonists & inhibitors, metabolism)
  • Remifentanil
  • Signal Transduction (physiology)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: