Tumor necrosis factor-α increases in the brain after intracerebral hemorrhage and thrombin stimulation

被引:162
作者
Hua, Y
Wu, JM
Keep, RF
Nakamura, T
Hoff, JT
Xi, GH
机构
[1] Univ Michigan, Dept Neurosurg, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Physiol, Ann Arbor, MI 48109 USA
关键词
brain edema; intracerebral hemorrhage; preconditioning; thrombin; tumor necrosis factor-alpha;
D O I
10.1227/01.NEU.0000197333.55473.AD
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
OBJECTIVE: The goals of this study were 1) to determine the effects of intracerebral hemorrhage (ICH) on brain tumor necrosis factor (TNF)-alpha levels, which are still controversial; 2) to investigate the role of TNF-alpha in ICH-induced brain injury; 3) to examine the effects of thrombin on brain TNF-alpha levels; and 4) to elucidate the role of TNF-alpha in thrombin-induced neuroprotection. METHODS: Autologous whole blood and thrombin were injected into the right caudate of rats or mice. Brain TNF-alpha was then determined by enzyme-linked immunosorbent assay and immunohistochemistry. Brain edema and neurological deficits were also examined. RESULTS: Perihematomal TNF-alpha levels increased after ICH. ICH-induced brain edema was less in TNF-alpha knockout mice compared with wild-type mice (P < 0.05). Intracerebral infusion of thrombin also caused an increase in brain TNF-alpha levels. Thrombin preconditioning reduced thrombin-induced brain edema, but this effect was not blocked by a neutralizing TNF-alpha antibody. CONCLUSION: Increase of perihematomal TNF-alpha levels contributes to brain edema formation after ICH. Thrombin may be a major mediator of ICH-induced TNF-alpha production, but thrombin-induced brain tolerance may not be TNF-alpha mediated.
引用
收藏
页码:542 / 548
页数:7
相关论文
共 38 条
  • [1] Tumor necrosis factor-alpha - A mediator of focal ischemic brain injury
    Barone, FC
    Arvin, B
    White, RF
    Miller, A
    Webb, CL
    Willette, RN
    Lysko, PG
    Feuerstein, GZ
    [J]. STROKE, 1997, 28 (06) : 1233 - 1244
  • [2] Inflammatory mediators and stroke: New opportunities for novel therapeutics
    Barone, FC
    Feuerstein, GZ
    [J]. JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1999, 19 (08) : 819 - 834
  • [3] A metalloproteinase disintegrin that releases tumour-necrosis factor-alpha from cells
    Black, RA
    Rauch, CT
    Kozlosky, CJ
    Peschon, JJ
    Slack, JL
    Wolfson, MF
    Castner, BJ
    Stocking, KL
    Reddy, P
    Srinivasan, S
    Nelson, N
    Boiani, N
    Schooley, KA
    Gerhart, M
    Davis, R
    Fitzner, JN
    Johnson, RS
    Paxton, RJ
    March, CJ
    Cerretti, DP
    [J]. NATURE, 1997, 385 (6618) : 729 - 733
  • [4] Molecular signatures of brain injury after intracerebral hemorrhage
    Castillo, J
    Dávalos, A
    Alvarez-Sabín, J
    Pumar, JM
    Leira, R
    Silva, Y
    Montaner, J
    Kase, CS
    [J]. NEUROLOGY, 2002, 58 (04) : 624 - 629
  • [5] Thrombin signalling and protease-activated receptors
    Coughlin, SR
    [J]. NATURE, 2000, 407 (6801) : 258 - 264
  • [6] Cognitive and behavioral assessment in experimental stroke research: will it prove useful?
    DeVries, AC
    Nelson, RJ
    Traystman, RJ
    Hurn, PD
    [J]. NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 2001, 25 (04) : 325 - 342
  • [7] Acute inflammatory reaction following experimental intracerebral hemorrhage in rat
    Gong, C
    Hoff, JT
    Keep, RF
    [J]. BRAIN RESEARCH, 2000, 871 (01) : 57 - 65
  • [8] The many faces of tumor necrosis factor in stroke
    Hallenbeck, JM
    [J]. NATURE MEDICINE, 2002, 8 (12) : 1363 - 1368
  • [9] Hua Y, 2003, ACT NEUR S, V86, P163
  • [10] Behavioral tests after intracerebral hemorrhage in the rat
    Hua, Y
    Schallert, T
    Keep, RF
    Wu, JM
    Hoff, JT
    Xi, GH
    [J]. STROKE, 2002, 33 (10) : 2478 - 2484