Effect of early and delayed decompressive craniectomy on secondary brain damage after controlled cortical impact in mice

被引:133
|
作者
Zweckberger, Klaus
Eroes, Christian
Zimmermann, Ricarda
Kim, Seong-Woong
Engel, Doortje
Plesnila, Nikolaus
机构
[1] Univ Munich, Med Ctr, Lab Expt Neurosurg, Dept Neurosurg, Munich, Germany
[2] Univ Munich, Med Ctr, Inst Surg Res, Munich, Germany
[3] Erasmus Univ, Med Ctr, Dept Neurosci, Rotterdam, Netherlands
关键词
brain edema; craniectomy; early craniectomy; mice; neuroprotection controlled cortical impact; secondary brain damage; traumatic brain injury;
D O I
10.1089/neu.2006.23.1083
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
The timing of decompressive craniectomy for the treatment of increased intracranial pressure (ICP) after traumatic brain injury (TBI) is a widely discussed clinical issue. Although we showed recently that early decompression is beneficial following experimental TBI, it remains unclear to what degree decompression craniectomy reduces secondary brain damage and if craniectomy is still beneficial when it is delayed by several hours as often inevitable during daily clinical practice. The aim of the current study was therefore to investigate the influence of craniectomy on secondary contusion expansion and brain edema formation and to determine the therapeutic window of craniectomy. Male C57/B16 mice were subjected to controlled cortical impact injury. Contusion volume, brain edema formation, and opening of the blood-brain barrier were investigated 2, 6, 12, and 24 h and 7 days after trauma. The effect of decompression craniectomy on secondary brain damage was studied in control mice (closed skull) and in animals craniotomized immediately or with a delay of 1, 3, or 8 It after trauma. Twenty-four hours after trauma:, the time point of maximal lesion expansion (+60% vs. 15 min after trauma) and brain edema formation (+3.0% water content vs. sham), contusion volume in craniotomized mice did not show any secondary expansion; that is, contusion volume was similar to that observed in mice sacrificed immediately after trauma (18.3 +/- 5.3 vs. 22.2 +/- 1.4 mm(3)). Furthermore, brain edema formation was reduced by 52% in craniotomized animals. The beneficial effect of craniectomy was still present even when treatment was delayed by up to 3 h after trauma (p < 0.05). The current study clearly demonstrates that early craniectomy prevents secondary brain damage and significantly reduces brain edema formation after experimental TBI. Evaluation of early craniectomy as a therapeutic option after TBI in humans may therefore be indicated.
引用
收藏
页码:1083 / 1093
页数:11
相关论文
共 50 条
  • [41] Cerebral metabolism after early decompression craniotomy following controlled cortical impact injury in rats
    Zweckberger, Klaus
    Hackenberg, Katharina
    Jung, Carla S.
    Hertle, Daniel N.
    Kiening, Karl L.
    Unterberg, Andreas W.
    Sakowitz, Oliver W.
    NEUROLOGICAL RESEARCH, 2011, 33 (08) : 875 - 880
  • [42] Neutrophils do not mediate blood-brain barrier permeability early after controlled cortical impact in rats
    Whalen, MJ
    Carlos, TM
    Kochanek, PM
    Clark, RSB
    Heineman, S
    Schiding, JK
    Franicola, D
    Memarzadeh, F
    Lo, W
    Marion, DW
    Dekosky, ST
    JOURNAL OF NEUROTRAUMA, 1999, 16 (07) : 583 - 594
  • [43] Inhaled nitric oxide reduces secondary brain damage after traumatic brain injury in mice
    Terpolilli, Nicole A.
    Kim, Seong-Woong
    Thal, Serge C.
    Kuebler, Wolfgang M.
    Plesnila, Nikolaus
    JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2013, 33 (02) : 311 - 318
  • [44] Necrostatin-1 reduces histopathology and improves functional outcome after controlled cortical impact in mice
    You, Zerong
    Savitz, Sean I.
    Yang, Jinsheng
    Degterev, Alexei
    Yuan, Junying
    Cuny, Gregory D.
    Moskowitz, Michael A.
    Whalen, Michael J.
    JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2008, 28 (09) : 1564 - 1573
  • [45] Fourteen-Day Mortality in Pediatric Patients with Traumatic Brain Injury After Early Decompressive Craniectomy: A Single-Center Retrospective Study
    Tang, Zhiji
    Huang, Qianliang
    Zhang, Jinshi
    Yang, Ruijin
    Wei, Wenjin
    Liu, Hongyi
    WORLD NEUROSURGERY, 2018, 119 : E389 - E394
  • [46] Fibronectin and laminin increase in the mouse brain after controlled cortical impact injury
    Tate, Ciara C.
    Tate, Matthew C.
    LaPlaca, Michelle C.
    JOURNAL OF NEUROTRAUMA, 2007, 24 (01) : 226 - 230
  • [47] Delayed inhibition of angiotensin II receptor type 1 reduces secondary brain damage and improves functional recovery after experimental brain trauma
    Timaru-Kast, Ralph
    Wyschkon, Sebastian
    Luh, Clara
    Schaible, Eva-Verena
    Lehmann, Florian
    Merk, Philipp
    Werner, Christian
    Engelhard, Kristin
    Thal, Serge C.
    CRITICAL CARE MEDICINE, 2012, 40 (03) : 935 - 944
  • [48] The Effect of Ubiquitin on Immune Response After Controlled Cortical Impact Injury
    Goelz, Leonie
    Casalis, Pablo A.
    Thomale, Ulrich-W.
    Misch, Martin
    JOURNAL OF TRAUMA-INJURY INFECTION AND CRITICAL CARE, 2011, 70 (05): : 1104 - 1111
  • [49] Influence of norepinephrine and dopamine on cortical perfusion, EEG activity, extracellular glutamate, and brain edema in rats after controlled cortical impact injury
    Kroppenstedt, SN
    Sakowitz, OW
    Thomale, UW
    Unterberg, AW
    Stover, JF
    JOURNAL OF NEUROTRAUMA, 2002, 19 (11) : 1421 - 1432
  • [50] Brain remodeling due to neuronal and astrocytic proliferation after controlled cortical injury in mice
    Kernie, SG
    Erwin, TM
    Parada, LF
    JOURNAL OF NEUROSCIENCE RESEARCH, 2001, 66 (03) : 317 - 326