Premium
Sensory neuronal phenotype in galanin receptor 2 knockout mice: focus on dorsal root ganglion neurone development and pain behaviour
Author(s) -
Shi TieJun Sten,
Hua Xiaoying,
Lu Xiaoying,
Malkmus Shelle,
Kinney Jeff,
Holmberg Kristina,
Wirz Sebastian,
Ceccatelli Sandra,
Yaksh Tony,
Bartfai Tamas,
Hökfelt Tomas
Publication year - 2006
Publication title -
european journal of neuroscience
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.346
H-Index - 206
eISSN - 1460-9568
pISSN - 0953-816X
DOI - 10.1111/j.1460-9568.2006.04593.x
Subject(s) - galanin , axotomy , dorsal root ganglion , galanin receptor , sciatic nerve , endocrinology , medicine , spinal cord , receptor , neuropeptide , knockout mouse , central nervous system , allodynia , nerve injury , neuroscience , hyperalgesia , biology , nociception
Galanin is a 29‐amino‐acid peptide expressed in dorsal root ganglion (DRG) neurones and spinal dorsal horn neurones. It affects pain threshold and has developmental and trophic effects. Galanin acts at three G‐protein‐coupled receptors, galanin receptors (GalR1–3), each expressed in the DRGs as suggested by in situ hybridization and/or reverse transcriptase‐polymerase chain reaction. The GalR2 knockout (–/–) mice permit studies on the contributions of this receptor subtype to the role of galanin at the spinal level. At 1 week after sciatic nerve transection (axotomy), there were 16–20% fewer neurones in intact and contralateral DRGs of –/– mice as compared with wild‐type (WT) mice. In addition, a significant neurone loss (26% reduction) was found in the ipsilateral DRGs of WT mice, whereas no further neurone loss was seen in –/– mice. Expression of several peptides has been examined after axotomy, including galanin, neuropeptide Y and two of its receptors as well as substance P, and no significant differences were found between –/– and WT mice in either ipsi‐ or contralateral DRGs, respectively. After thermal injury and spinal nerve ligation, onset and duration of hyperalgesia in the injured paw were similar in GalR2–/– and WT animals. Recovery from spinal nerve ligation‐caused allodynia had the same kinetics in –/– and WT animals. These data are in line with earlier observations from the peripheral and central nervous system, suggesting that galanin actions mediated by GalR2 subtype are of importance in neurodevelopment and neuroprotection.