Plasticity of α2-adrenergic spinal antinociception following nerve injury: Selective, bidirectional interaction with the delta opioid receptor-Reference-Cited by-同舟云学术

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Plasticity of α2-adrenergic spinal antinociception following nerve injury: Selective, bidirectional interaction with the delta opioid receptor

Published:2015-01 Issue: Volume:1594 Page:190-203
ISSN:0006-8993
Container-title:Brain Research
language:en
Short-container-title:Brain Research

Author:

Aira Zigor,Barrenetxea Teresa,Buesa Itsaso,Azkue Jon Jatsu

Funder

Government of the Basque Country

Ayudas a Grupos de Investigación del Sistema Universitario Vasco

University of the Basque Country

Publisher

Elsevier BV

Subject

Developmental Biology,Neurology (clinical),Molecular Biology,General Neuroscience

Reference105 articles.

1. Time-dependent cross talk between spinal serotonin 5-HT2A receptor and mGluR1 subserves spinal hyperexcitability and neuropathic pain after nerve injury;Aira;J. Neurosci.,2012

2. Transient, 5-HT2B receptor-mediated facilitation in neuropathic pain: up-regulation of PKCγ and engagement of the NMDA receptor in dorsal horn neurons;Aira;Pain,2013

3. Coupling of serotonergic input to NMDA receptor-phosphorylation following peripheral nerve injury via rapid, synaptic up-regulation of ND2;Aira;Exp. Neurol.,2014

4. The use of total protein stains as loading controls: an alternative to high-abundance single-protein controls in semi-quantitative immunoblotting;Aldridge;J. Neurosci. Methods,2008

5. Effect of resiniferatoxin on the noxious heat threshold temperature in the rat: a novel heat allodynia model sensitive to analgesics;Almási;Br. J. Pharmacol.,2003

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