Endoneurial injection of TNF-alpha produces neuropathic pain behaviors

被引:360
作者
Wagner, R
Myers, RR
机构
[1] UNIV CALIF SAN DIEGO,DEPT ANESTHESIOL,LA JOLLA,CA 92093
[2] UNIV CALIF SAN DIEGO,DEPT PATHOL NEUROPATHOL,LA JOLLA,CA 92093
[3] VET ADM MED CTR,LA JOLLA,CA 92093
关键词
degeneration; demyelination; hyperalgesia; neuropathic pain; neuropathy; TNF;
D O I
10.1097/00001756-199611250-00018
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
THE inflammatory component of peripheral nerve injury may affect the development of local neuropathologic changes as well as the onset of hyperalgesia, the characteristic features of experimental neuropathic pain states. The goal of this study was to determine whether local sciatic injection of the proinflammatory cytokine tumor necrosis factor (TNF)-alpha could reproduce the nociceptive behaviors and endoneurial pathology found following experimental nerve injuries. TNF injection caused significant thermal hyperalgesia and mechanical allodynia for 3 days post-injection in association with nerve edema, splitting of myelin lamellae with vacuolization, Schwann cell injury, fibroblast and macrophage activation, and phagocytosis of lipid debris. The data show that subperineurial injection of TNF proximal to peripheral sensory receptors generates the transient display of behaviors and endoneurial pathologies found in experimental painful nerve injury, and implicates local TNF in the pathologies of neuropathic pain.
引用
收藏
页码:2897 / 2901
页数:5
相关论文
共 23 条
  • [1] THE SPECTRUM OF FIBER LOSS IN A MODEL OF NEUROPATHIC PAIN IN THE RAT - AN ELECTRON-MICROSCOPIC STUDY
    BASBAUM, AI
    GAUTRON, M
    JAZAT, F
    MAYES, M
    GUILBAUD, G
    [J]. PAIN, 1991, 47 (03) : 359 - 367
  • [2] BENNETT GJ, 1988, PAIN, V33, P498
  • [3] BEUTLER B, 1989, ANNU REV IMMUNOL, V7, P625, DOI 10.1146/annurev.iy.07.040189.003205
  • [4] IS LARGE MYELINATED FIBER LOSS ASSOCIATED WITH HYPERALGESIA IN A MODEL OF EXPERIMENTAL PERIPHERAL NEUROPATHY IN THE RAT
    COGGESHALL, RE
    DOUGHERTY, PM
    POVER, CM
    CARLTON, SM
    [J]. PAIN, 1993, 52 (02) : 233 - 242
  • [5] CUNHA Q, 1992, BRIT J PHARMACOL, V107, P660
  • [6] HYPOXEMIA IN THE ABSENCE OF BLOOD-LOSS OR SIGNIFICANT HYPOTENSION CAUSES INFLAMMATORY CYTOKINE RELEASE
    ERTEL, W
    MORRISON, MH
    AYALA, A
    CHAUDRY, IH
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 1995, 269 (01) : R160 - R166
  • [7] A NEW AND SENSITIVE METHOD FOR MEASURING THERMAL NOCICEPTION IN CUTANEOUS HYPERALGESIA
    HARGREAVES, K
    DUBNER, R
    BROWN, F
    FLORES, C
    JORIS, J
    [J]. PAIN, 1988, 32 (01) : 77 - 88
  • [8] FORMATION OF ION-PERMEABLE CHANNELS BY TUMOR-NECROSIS-FACTOR-ALPHA
    KAGAN, BL
    BALDWIN, RL
    MUNOZ, D
    WISNIESKI, BJ
    [J]. SCIENCE, 1992, 255 (5050) : 1427 - 1430
  • [9] INHIBITION OF GAP JUNCTIONAL INTERCELLULAR COMMUNICATION BETWEEN PRIMARY HUMAN SMOOTH-MUSCLE CELLS BY TUMOR-NECROSIS-FACTOR-ALPHA
    MENSINK, A
    DEHAAN, LHJ
    LAKEMOND, CMM
    KOELMAN, CA
    KOEMAN, JH
    [J]. CARCINOGENESIS, 1995, 16 (09) : 2063 - 2067
  • [10] THE ROLE OF FOCAL NERVE ISCHEMIA AND WALLERIAN DEGENERATION IN PERIPHERAL-NERVE INJURY PRODUCING HYPERESTHESIA
    MYERS, RR
    YAMAMOTO, T
    YAKSH, TL
    POWELL, HC
    [J]. ANESTHESIOLOGY, 1993, 78 (02) : 308 - 316