Abstract | BACKGROUND: 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: RESULTS: CONCLUSIONS: Our findings indicated that ephrinB/EphB signalling is involved in RIH. EphrinB/EphB signalling might be the upstream of NMDA receptor.
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Authors | W S Xia, Y N Peng, L H Tang, L S Jiang, L N Yu, X L Zhou, F J Zhang, M Yan |
Journal | European journal of pain (London, England)
(Eur J Pain)
Vol. 18
Issue 9
Pg. 1231-9
(Oct 2014)
ISSN: 1532-2149 [Electronic] England |
PMID | 24737575
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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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
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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)
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