The expression of tumor necrosis factor-alpha in the rat brain after fluid percussive injury

被引:31
作者
Kita, T [1 ]
Liu, L [1 ]
Tanaka, N [1 ]
Kinoshita, Y [1 ]
机构
[1] UNIV OCCUPAT & ENVIRONM HLTH,SCH MED,DEPT NEUROSURG,KITAKYUSHU,FUKUOKA 807,JAPAN
关键词
traumatic head injury; tumor necrosis factor-alpha; blood-brain barrier; fluid percussion device; microglial cell;
D O I
10.1007/s004140050093
中图分类号
DF [法律]; D9 [法律]; R [医药、卫生];
学科分类号
0301 ; 10 ;
摘要
To investigate the role of tumor necrosis factor-alpha (TNF alpha) after traumatic head injury in rats, moderate brain injury of 1000 mmHg was generated by an original fluid percussion injury device, TNF alpha levels in cerebrospinal fluid (CSF) gradually increased during the first 1 h, rose to a maximal elevation at 3 h and 6 h and returned to basal values by 24 h. Horseradish peroxidase tracer experiments revealed that primary microvascular damage appeared as early as 15 min after impact, but rapidly recovered and 1 h after impact secondary microvascular damage occurred in the hippocampus and parasagittal cortex. By immunoelectron microscopy, TNF alpha reactions were detected in the lysosomes of microglia accumulated at the impact site of the cortex 30 min after impact, and 1 h after impact these reactions were mainly detected at the glial cells (such as microglia and astrocytes) in the hippocampus and parasagittal cortex. Therefore the delayed microvascular damage observed in sites remote from the impact may be induced by TNF alpha which is synthesized mainly by glial cells, The present study suggests that TNF alpha conveyed from the microglial cells is one cofactor contributing to the fluid percussive brain edema formation after moderate brain injury.
引用
收藏
页码:305 / 311
页数:7
相关论文
共 39 条
  • [1] ALTERED IMMUNOEXPRESSION OF MICROGLIA AND MACROPHAGES AFTER MILD HEAD-INJURY
    AIHARA, N
    HALL, JJ
    PITTS, LH
    FUKUDA, K
    NOBLE, LJ
    [J]. JOURNAL OF NEUROTRAUMA, 1995, 12 (01) : 53 - 63
  • [2] TUMOR-NECROSIS-FACTOR-ALPHA MEDIATES THE RELEASE OF BIOACTIVE TRANSFORMING GROWTH-FACTOR-BETA IN MURINE MICROGLIAL CELL-CULTURES
    CHAO, CC
    HU, SX
    SHENG, WS
    TSANG, M
    PETERSON, PK
    [J]. CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1995, 77 (03): : 358 - 365
  • [3] EARLY MICROVASCULAR AND NEURONAL CONSEQUENCES OF TRAUMATIC BRAIN INJURY - A LIGHT AND ELECTRON-MICROSCOPIC STUDY IN RATS
    DIETRICH, WD
    ALONSO, O
    HALLEY, M
    [J]. JOURNAL OF NEUROTRAUMA, 1994, 11 (03) : 289 - 301
  • [4] A FLUID PERCUSSION MODEL OF EXPERIMENTAL BRAIN INJURY IN THE RAT
    DIXON, CE
    LYETH, BG
    POVLISHOCK, JT
    FINDLING, RL
    HAMM, RJ
    MARMAROU, A
    YOUNG, HF
    HAYES, RL
    [J]. JOURNAL OF NEUROSURGERY, 1987, 67 (01) : 110 - 119
  • [5] BRAIN KININOGEN FOLLOWING EXPERIMENTAL BRAIN INJURY - EVIDENCE FOR A SECONDARY EVENT
    ELLIS, EF
    CHAO, J
    HEIZER, ML
    [J]. JOURNAL OF NEUROSURGERY, 1989, 71 (03) : 437 - 442
  • [6] Experimental brain injury induces differential expression of tumor necrosis factor-alpha mRNA in the CNS
    Fan, L
    Young, PR
    Barone, FC
    Feuerstein, GZ
    Smith, DH
    McIntosh, TK
    [J]. MOLECULAR BRAIN RESEARCH, 1996, 36 (02): : 287 - 291
  • [7] FEUERSTEIN GZ, 1994, CEREBROVAS BRAIN MET, V6, P341
  • [8] FUKUDA K, 1993, NEUROTRAUMA, V16, P19
  • [9] GOODMAN JC, 1990, J NEUROIMMUNOL, V30, P213
  • [10] CNTF REGULATION OF ASTROGLIOSIS AND THE ACTIVATION OF MICROGLIA IN THE DEVELOPING RAT CENTRAL-NERVOUS-SYSTEM
    KAHN, MA
    ELLISON, JA
    SPEIGHT, GJ
    DEVELLIS, J
    [J]. BRAIN RESEARCH, 1995, 685 (1-2) : 55 - 67