The ontogeny of neuropathic pain: Postnatal onset of mechanical allodynia in rat spared nerve injury (SNI) and chronic constriction injury (CCI) models

被引:95
作者
Howard, RF
Walker, SM
Mota, PM
Fitzgerald, M
机构
[1] Great Ormond St Hosp Sick Children, Dept Anaesthesia, London WC1N 2JH, England
[2] Inst Child Hlth, London WC1N 2JH, England
[3] UCL, Dept Anat & Dev Biol, London WC1E 6BT, England
关键词
neuropathic pain; mechanical allodynia; postnatal development;
D O I
10.1016/j.pain.2005.03.016
中图分类号
R614 [麻醉学];
学科分类号
100217 [麻醉学];
摘要
Neuropathic pain is known to occur in children but remains Poorly understood and treated. The aim here was to establish a model of neuropathic pain in neonatal and young rodents. In the adult the spared nerve injury (SNI) model produced robust mechanical allodynia measured as a fall in cutaneous sensory threshold to 1617( of controls. within one postoperative day and lasting at least 29 days. In contrast, animals aged 3, 10 and 21 days at the time of surgery did not display equivalent allodynia at any time tip to 29 days later. A small, transient bilateral increased cutaneous sensitivity was observed at day 7 in P10 and P21 animals hill this had gone by 14 days. SNI performed at 33 days led to a significant and persistent allodynia with the threshold falling to 5514 of control values, A similar lack or neuropathic pain behaviour in younger animals was observed using the chronic constriction injury (CCI) model, which production a clear allodynia in adult rats but no change in hindpaw sensitivity when performed at 10 days of age. Mechanical allodynia, can be evoked in very young animals with inflammatory pain, so this developmental profile is selective for peripheral neuropathic pain and suggests a remarkable ability in young animals to compensate for the sensory consequences of nerve injury. The results are consistent with neonatal responses to nerve injury: further study of underlying mechanisms are likely to yield important information about the pathogenesis and treatment of neuropathic pain. (c) 2005 International Association for the Study of Pain. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:382 / 389
页数:8
相关论文
共 46 条
[1]
Restoration of sensory function and lack of longterm chronic pain syndromes after brachial plexus injury in human neonates [J].
Anand, P ;
Birch, R .
BRAIN, 2002, 125 :113-122
[2]
The postnatal reorganization of primary afferent input and dorsal horn cell receptive fields in the rat spinal cord is an activity-dependent process [J].
Beggs, S ;
Torsney, C ;
Drew, LJ ;
Fitzgerald, M .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2002, 16 (07) :1249-1258
[3]
A PERIPHERAL MONONEUROPATHY IN RAT THAT PRODUCES DISORDERS OF PAIN SENSATION LIKE THOSE SEEN IN MAN [J].
BENNETT, GJ ;
XIE, YK .
PAIN, 1988, 33 (01) :87-107
[4]
BERDE CB, 2003, NEUROPATHIC PAIN CHI, P621
[5]
Pain following human brachial plexus injury with spinal cord root avulsion and the effect of surgery [J].
Berman, JS ;
Birch, R ;
Anand, P .
PAIN, 1998, 75 (2-3) :199-207
[6]
The onset of diffuse noxious inhibitory controls in postnatal rat pups: a C-Fos study [J].
Boucher, T ;
Jennings, E ;
Fitzgerald, M .
NEUROSCIENCE LETTERS, 1998, 257 (01) :9-12
[7]
Mechanism in neuropathic pain [J].
Bridges, D ;
Thompson, SWN ;
Rice, ASC .
BRITISH JOURNAL OF ANAESTHESIA, 2001, 87 (01) :12-26
[8]
Management of chronic pain in children [J].
Chalkiadis, GA .
MEDICAL JOURNAL OF AUSTRALIA, 2001, 175 (09) :476-+
[9]
Decosterd I, 2004, ANESTH ANALG, V99, P457
[10]
Spared nerve injury: an animal model of persistent peripheral neuropathic pain [J].
Decosterd, I ;
Woolf, CJ .
PAIN, 2000, 87 (02) :149-158