Partial sciatic nerve transection as a model of neuropathic pain: a qualitative and quantitative neuropathological study

被引:88
作者
Lindenlaub, T [1 ]
Sommer, C [1 ]
机构
[1] Univ Wurzburg, Neurol Klin, D-97080 Wurzburg, Germany
关键词
chronic constriction injury; epineurial inflammation; neuroma; pain-related behavior; partial sciatic transection;
D O I
10.1016/S0304-3959(00)00354-7
中图分类号
R614 [麻醉学];
学科分类号
100217 [麻醉学];
摘要
One of the most commonly used experimental animal models for neuropathic pain is the chronic constriction injury (CCI) where four loose ligatures are tied around the sciatic nerve. One disadvantage of this model is the introduction of foreign material into the wound, which causes a local inflammatory reaction. Thus the distinction between the neuropathic and the inflammatory component of pain is difficult in this model. In order to produce a pure nerve lesion, we performed a partial sciatic nerve transection (PST; a modification of the Seltzer model) in female Sprague-Dawley rats and compared behavior and nerve pathology. These rats developed thermal hyperalgesia and mechanical allodynia comparable to the CCI model. Recovery of these symptoms was found between days 40 and 60 after the nerve lesion. Som-animals still showed symptoms on day 101, which was associated with a neuroma formation. The main pathological findings in the endoneurium in nerve segments distal to the lesion were edema, loss of myelinated fibers and increase in endoneurial cells, especially macrophages. In the epineuriurn the number of macrophages was strikingly increased after CCI compared with PST, indicating that the response of the immune system is different in a structural lesion with and without foreign material. In conclusion, PST is a pure nerve injury model without an epineurial inflammatory component due to foreign material and is therefore well suited for studying the role of local endoneurial processes in the development and maintenance of neuropathic pain. Also, the importance of regeneration in the termination of hyperalgesia can convincingly be shown in this model. (C) 2000 International Association for the Study of Pain. Published by Elsevier Science B.V. All nights reserved.
引用
收藏
页码:97 / 106
页数:10
相关论文
共 36 条
[1]
PAINFUL NEUROPATHY - C-NOCICEPTOR ACTIVITY MAY NOT BE NECESSARY TO MAINTAIN CENTRAL MECHANISMS ACCOUNTING FOR DYNAMIC-MECHANICAL ALLODYNIA [J].
BARON, R ;
MAIER, C .
CLINICAL JOURNAL OF PAIN, 1995, 11 (01) :63-69
[2]
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
[3]
Bove GM, 1997, PAIN FORUM, V6, P181
[4]
Influence of physical parameters of nerve chambers on peripheral nerve regeneration and reinnervation [J].
Buti, M ;
Verdu, E ;
Labrador, RO ;
Vilches, JJ ;
Fores, J ;
Navarro, X .
EXPERIMENTAL NEUROLOGY, 1996, 137 (01) :26-33
[5]
ROLE OF PERI-AXONAL INFLAMMATION IN THE DEVELOPMENT OF THERMAL HYPERALGESIA AND GUARDING BEHAVIOR IN A RAT MODEL OF NEUROPATHIC PAIN [J].
CLATWORTHY, AL ;
ILLICH, PA ;
CASTRO, GA ;
WALTERS, ET .
NEUROSCIENCE LETTERS, 1995, 184 (01) :5-8
[6]
IS LARGE MYELINATED FIBER LOSS ASSOCIATED WITH HYPERALGESIA IN A MODEL OF EXPERIMENTAL PERIPHERAL NEUROPATHY IN THE RAT [J].
COGGESHALL, RE ;
DOUGHERTY, PM ;
POVER, CM ;
CARLTON, SM .
PAIN, 1993, 52 (02) :233-242
[7]
The effect of site and type of nerve injury on spinal glial activation and neuropathic pain behavior [J].
Colburn, RW ;
Rickman, AJ ;
DeLeo, JA .
EXPERIMENTAL NEUROLOGY, 1999, 157 (02) :289-304
[8]
PERIOPERATIVE NERVE LESIONS [J].
DAWSON, DM ;
KRARUP, C .
ARCHIVES OF NEUROLOGY, 1989, 46 (12) :1355-1360
[9]
DEVOR M, 1993, J NEUROSCI, V13, P1976
[10]
THE UP-AND-DOWN METHOD FOR SMALL SAMPLES [J].
DIXON, WJ .
JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION, 1965, 60 (312) :967-978