Dynamic changes in brain glucose and lactate in pericontusional areas of the human cerebral cortex, monitored with rapid sampling on-line microdialysis: relationship with depolarisation-like events

被引:110
作者
Parkin, MC
Hopwood, SE
Jones, DA
Hashemi, P
Landolt, H
Fabricius, M
Lauritzen, M
Boutelle, MG
Strong, AJ
机构
[1] Kings Coll Hosp London, Dept Neurosurg, London SE5 9RS, England
[2] Kings Coll Hosp London, Dept Chem, London SE5 9RS, England
[3] Kantonsspital Aarau, Dept Neurosurg, Aarau, Switzerland
[4] Glostrup Univ Hosp, Dept Clin Neurophysiol, Copenhagen, Denmark
关键词
brain-trauma; electroencephalogram; glucose; human; lactate; microdialysis; spreading-cortical-depression;
D O I
10.1038/sj.jcbfm.9600051
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The pathophysiology of peri-lesion boundary zones in acute brain injury is highly dynamic, and it is now clear that spreading-depression-like events occur frequently in areas of cerebral cortex adjacent to contusions in the injured human brain. An automated method to assay microdialysate from peri-lesion cerebral cortex in 11 patients with intracranial haematomas requiring surgery was used. Perfusate (2 mu L/min) flowed directly into a flow-injection system for assay of glucose and lactate at intervals typically of 30 secs each. Four channels of electrocorticogram (ECoG) were recorded from a subdural strip adjacent to the catheter. Several patterns of change in metabolites were identified in different time domains. Overall, the number of transient lactate events was significantly correlated with the number of glucose events (r(2) = 0.48, P= 0.027, n = 10). Progressive reduction in dialysate glucose was very closely correlated with the aggregate number of ECoG events (r(2) = 0.76, P = 0.0004, n = 11). It is proposed that the recently documented adverse impact of low dialysate glucose on clinical outcome may be because of recurrent, spontaneous spreading-depression-like events in the perilesion cortex.
引用
收藏
页码:402 / 413
页数:12
相关论文
共 46 条
[1]   Striking differences in glucose and lactate levels between brain extracellular fluid and plasma in conscious human subjects: Effects of hyperglycemia and hypoglycemia [J].
Abi-Saab, WM ;
Maggs, DG ;
Jones, T ;
Jacob, R ;
Srihari, V ;
Thompson, J ;
Kerr, D ;
Leone, P ;
Krystal, JH ;
Spencer, DD ;
During, MJ ;
Sherwin, RS .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2002, 22 (03) :271-279
[2]   Induction of spreading depression in the ischemic hemisphere following experimental middle cerebral artery occlusion: Effect on infarct morphology [J].
Back, T ;
Ginsberg, MD ;
Dietrich, WD ;
Watson, BD .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1996, 16 (02) :202-213
[3]   BRAIN MICRODIALYSIS [J].
BENVENISTE, H .
JOURNAL OF NEUROCHEMISTRY, 1989, 52 (06) :1667-1679
[4]   Cerebral hyperglycolysis following severe traumatic brain injury in humans: A positron emission tomography study [J].
Bergsneider, M ;
Hovda, DA ;
Shalmon, E ;
Kelly, DF ;
Vespa, PM ;
Martin, NA ;
Phelps, ME ;
McArthur, DL ;
Caron, MJ ;
Kraus, JF ;
Becker, DP .
JOURNAL OF NEUROSURGERY, 1997, 86 (02) :241-251
[5]   KINETICS OF UNIDIRECTIONAL GLUCOSE TRANSPORT INTO ISOLATED DOG BRAIN [J].
BETZ, AL ;
GILBOE, DD ;
YUDILEVICH, DL ;
DREWES, LR .
AMERICAN JOURNAL OF PHYSIOLOGY, 1973, 225 (03) :586-592
[6]  
Boutelle MG, 1996, ACT NEUR S, V67, P13
[7]   EXTRACELLULAR POTASSIUM ACTIVITY, EVOKED-POTENTIAL AND TISSUE BLOOD-FLOW - RELATIONSHIPS DURING PROGRESSIVE ISCHEMIA IN BABOON CEREBRAL-CORTEX [J].
BRANSTON, NM ;
STRONG, AJ ;
SYMON, L .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1977, 32 (03) :305-321
[8]   STEADY-STATE THEORY FOR QUANTITATIVE MICRODIALYSIS OF SOLUTES AND WATER INVIVO AND INVITRO [J].
BUNGAY, PM ;
MORRISON, PF ;
DEDRICK, RL .
LIFE SCIENCES, 1990, 46 (02) :105-119
[9]  
BUNGAY PM, 2001, INT C IN VIV METH MO, P91
[10]   Potassium-induced cortical spreading depressions during focal cerebral ischemia in rats: Contribution to lesion growth assessed by diffusion-weighted NMR and biochemical imaging [J].
Busch, E ;
Gyngell, ML ;
Eis, M ;
HoehnBerlage, M ;
Hossmann, KA .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1996, 16 (06) :1090-1099