Mechanical hyperalgesia after an L5 spinal nerve lesion in the rat is not dependent on input from injured nerve fibers

被引:233
作者
Li, YB
Dorsi, MJ
Meyer, RA
Belzberg, AJ
机构
[1] Johns Hopkins Univ, Sch Med, Dept Neurosurg, Baltimore, MD 21287 USA
[2] Johns Hopkins Univ, Appl Phys Lab, Laurel, MD USA
关键词
mechanical hyperalgesia; L5; ligation; dorsal rhizotomy; dermatome; neuropathic pain; wallerian degeneration;
D O I
10.1016/S0304-3959(00)00250-5
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
An injury to a peripheral nerve in animals often leads to signs of neuropathic pain including hyperalgesia to heat, cold and mechanical stimuli. The role of injured and intact nerve fibers in mechanical hyperalgesia was evaluated in rats subjected to an L5 spinal nerve ligation-and-cut ('modified SNL lesion'). To assess the contribution of injured afferents, an L5 dorsal rhizotomy was performed immediately before, or 7 days after the modified SNL lesion. To study the role of adjacent intact spinal nerves, an L4 dorsal rhizotomy was performed 7 days after the modified SNL lesion. The up-down method of Dixon (Dixon WJ, Annu Rev Pharmacol Toxicol 1980;20:441-462) was used to measure the paw withdrawal threshold to mechanical stimuli at three sites on the rat hindpaw corresponding to the L3, L4, and L5 dermatomes. We found that the modified SNL lesion produced a significant, lasting (>20 days) decrease of the mechanical withdrawal threshold. The severity and duration of mechanical hyperalgesia varied across testing sites. The L5 and JA dermatome test sites developed the most severe and lasting mechanical hyperalgesia. In contrast, the L3 testing site developed significantly less severe and shorter lasting mechanical hyperalgesia. L5 dorsal rhizotomy, by itself, produced a transient decrease in mechanical withdrawal thresholds. L5 dorsal rhizotomy performed before, or 7 days after, the modified SNL lesion did not prevent or resolve the observed decrease in mechanical withdrawal thresholds. L4 dorsal rhizotomy performed 7 days after the modified SNL lesion resulted in an immediate reversal of mechanical withdrawal thresholds back to baseline values. These results suggest that, after L5 spinal nerve ligation-and-cut, mechanical hyperalgesia develops and persists independent of input from injured afferents. We propose that the Wallerian degeneration that develops after a nerve injury leads to interactions between the degenerating fibers of the injured spinal nerve and the intact fibers of adjacent spinal nerves. This leads to changes in the intact fibers that play a critical role for both initiation and maintenance of mechanical hyperalgesia. (C) 2000 International Association for the Study of Pain. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:493 / 502
页数:10
相关论文
共 42 条
  • [1] Uninjured C-fiber nociceptors develop spontaneous activity and α-adrenergic sensitivity following L6 spinal nerve ligation in monkey
    Ali, Z
    Ringkamp, M
    Hartke, TV
    Chien, HF
    Flavahan, NA
    Campbell, JN
    Meyer, RA
    [J]. JOURNAL OF NEUROPHYSIOLOGY, 1999, 81 (02) : 455 - 466
  • [2] SKIN VASCULAR REACTIVITY TO THE NEUROPEPTIDE SUBSTANCE-P IN RATS WITH PERIPHERAL MONONEUROPATHY
    BASILE, S
    KHALIL, Z
    HELME, RD
    [J]. PAIN, 1993, 52 (02) : 217 - 222
  • [3] Nerve growth factor induced hyperalgesia in the rat hind paw is dependent on circulating neutrophils
    Bennett, G
    al-Rashed, S
    Hoult, JRS
    Brain, SD
    [J]. PAIN, 1998, 77 (03) : 315 - 322
  • [4] A PERIPHERAL MONONEUROPATHY IN RAT THAT PRODUCES DISORDERS OF PAIN SENSATION LIKE THOSE SEEN IN MAN
    BENNETT, GJ
    XIE, YK
    [J]. PAIN, 1988, 33 (01) : 87 - 107
  • [5] Nerve growth factor evokes hyperalgesia in mice lacking the low-affinity neurotrophin receptor p75
    Bergmann, I
    Reiter, R
    Toyka, KV
    Koltzenburg, M
    [J]. NEUROSCIENCE LETTERS, 1998, 255 (02) : 87 - 90
  • [6] DISCHARGE PATTERN OF AFFERENT-FIBERS FROM A NEUROMA
    BLUMBERG, H
    JANIG, W
    [J]. PAIN, 1984, 20 (04) : 335 - 353
  • [7] The effect of site and type of nerve injury on spinal glial activation and neuropathic pain behavior
    Colburn, RW
    Rickman, AJ
    DeLeo, JA
    [J]. EXPERIMENTAL NEUROLOGY, 1999, 157 (02) : 289 - 304
  • [8] Devor M., 1999, TXB PAIN, V4th, P129
  • [9] EFFICIENT ANALYSIS OF EXPERIMENTAL-OBSERVATIONS
    DIXON, WJ
    [J]. ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 1980, 20 : 441 - 462
  • [10] HILLMAN P, 1969, EXP BRAIN RES, V9, P284