Standardized induction of subarachnoid hemorrhage in mice by intracranial pressure monitoring

被引:75
作者
Feiler, Sergej
Friedrich, Benjamin
Schoeller, Karsten
Thal, Serge C.
Plesnila, Nikolaus
机构
[1] Univ Munich, Inst Surg Res, Med Ctr Grosshadern, D-81377 Munich, Germany
[2] Univ Munich, Dept Neurosurg, Med Ctr Grosshadern, D-81377 Munich, Germany
关键词
Subarachnoid hemorrhage; Mouse; Model; Intracranial pressure; Neuronal cell death; Functional outcome; CUZN-SUPEROXIDE DISMUTASE; CEREBRAL VASOSPASM; MURINE MODEL; RAT; ARTERIES; SYNTHASE; STROKE;
D O I
10.1016/j.jneumeth.2010.05.005
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background and purpose: Subarachnoid hemorrhage (SAH) is the subtype of stroke with the most unfavorable outcome but the least well investigated molecular pathophysiology. Among others, not sufficiently well standardized in vivo models suitable for the use with transgenic animals may be responsible for this situation. Therefore the aim of the current study was to detect suitable intra-operative parameters for the controlled and standardized induction of SAH in mice and to characterize the long-term functional and histopathological outcome of mice subjected to this procedure. Methods: Experimental study in mice using the intraluminal Circle of Willis perforation (CWp) model of SAH. Results: SAH induced a sharp increase of intracranial pressure (ICP) from 5.1 +/- 1.2 to 78.5 +/- 9.3 mmHg (mean +/- SD; p <0.05), a concomitant drop of cerebral blood flow (rCBF) by 81 +/- 4% (p <0.05), and a significant Cushing reflex response (p <0.05). rCBF measurements alone could not reliably detect SAH. SAH resulted in significant brain edema formation (brain water content increase at 72 h: 2.9 +/- 0.9%; p <0.05), loss of hippocampal neurons (CA1: -56%, CA2: -55%; CA3: -72%; 7 days; p < 0.05), severe neurological dysfunction over 7 days, and a mortality of 30%. Conclusions: Our results indicate that CWp in mice can be standardized by intra-operative ICP monitoring. CWp leads to prolonged intracranial hypertension, selective neuronal cell death in the hippocampus, and severe neurological dysfunction. CWp in mice with ICP monitoring may therefore become a valuable tool for future investigations of the molecular pathophysiology of SAH. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:164 / 170
页数:7
相关论文
共 27 条
[1]  
ALTAY T, 2009, J NEUROSCI METHODS
[2]   SMALL ANIMAL-MODEL FOR INVESTIGATION OF SUBARACHNOID HEMORRHAGE AND CEREBRAL VASOSPASM [J].
BARRY, KJ ;
GOGJIAN, MA ;
STEIN, BM .
STROKE, 1979, 10 (05) :538-541
[3]   CORTICAL BLOOD-FLOW AND CEREBRAL PERFUSION-PRESSURE IN A NEW NONCRANIOTOMY MODEL OF SUBARACHNOID HEMORRHAGE IN THE RAT [J].
BEDERSON, JB ;
GERMANO, IM ;
GUARINO, L .
STROKE, 1995, 26 (06) :1086-1091
[4]   Hypertonic fluid resuscitation from subarachnoid hemorrhage in rats: A comparison between small volume resuscitation and mannitol [J].
Bermueller, C ;
Thal, SC ;
Plesnila, N ;
Schmid-Elsaesser, R ;
Kreimeier, U ;
Zausinger, S .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 2006, 241 (1-2) :73-82
[5]   INITIAL AND RECURRENT BLEEDING ARE THE MAJOR CAUSES OF DEATH FOLLOWING SUBARACHNOID HEMORRHAGE [J].
BRODERICK, JP ;
BROTT, TG ;
DULDNER, JE ;
TOMSICK, T ;
LEACH, A .
STROKE, 1994, 25 (07) :1342-1347
[6]   Subarachnoid Hemorrhage Is It Time for a New Direction? [J].
Cahill, Julian ;
Zhang, John H. .
STROKE, 2009, 40 (03) :S86-S87
[7]   Global cerebral edema after subarachnoid hemorrhage - Frequency, predictors, and impact on outcome [J].
Claassen, J ;
Carhuapoma, JR ;
Kreiter, KT ;
Du, EY ;
Connolly, ES ;
Mayer, SA .
STROKE, 2002, 33 (05) :1225-1232
[8]   SUBARACHNOID HEMORRHAGE IN THE RAT - ANGIOGRAPHY AND FLUORESCENCE MICROSCOPY OF THE MAJOR CEREBRAL-ARTERIES [J].
DELGADO, TJ ;
BRISMAR, J ;
SVENDGAARD, NA .
STROKE, 1985, 16 (04) :595-602
[9]  
DORSCH N, 1989, Neurological Research, V11, P201
[10]   A novel apoE-derived therapeutic reduces vasospasm and improves outcome in a murine model of subarachnoid hemorrhage [J].
Gao, Junling ;
Wang, Haichen ;
Sheng, Huaxin ;
Lynch, John R. ;
Warner, David S. ;
Durham, Lori ;
Vitek, Michael P. ;
Laskowitz, Daniel T. .
NEUROCRITICAL CARE, 2006, 4 (01) :25-31