Mouse model of subarachnoid hemorrhage associated cerebral vasospasm: Methodological analysis

被引:89
作者
Parra, A
McGirt, MJ
Sheng, HX
Laskowitz, DT
Pearlstein, RD
Warner, DS
机构
[1] Duke Univ, Med Ctr, Dept Anesthesiol, Durham, NC 27710 USA
[2] Duke Univ, Med Ctr, Dept Med Neurol, Durham, NC 27710 USA
[3] Duke Univ, Med Ctr, Dept Surg Neurosurg, Durham, NC 27710 USA
[4] Duke Univ, Sch Med, Durham, NC 27706 USA
关键词
mouse; brain; subarachnoid hemorrhage; vasospasm;
D O I
10.1179/016164102101200276
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The transgenic mouse has been used to study subarachnoid hemorrhage (SAH) induced delayed cerebral vasospasm (DCV). Methodological parameters have not been analyzed to validate this model and associated neurological deficits have not been described. We introduce a technique to quantify DCV and associated neurological deficits. C57BL/6J mice were subjected to SAH or sham surgery. Seventy-two hours later, the vasculature was cast in situ with India ink/gelatin at perfusion pressures of 40-60, 60-80, or 100-120 mmHg. Mice were perfused with and without microfiltration. Additional mice underwent grading of SAH size, measurement of vascular diameters, and neurological examination (score range 5-27; 27 = normal). When cast at 60-80 mmHg, SAH was associated with an intraluminal cross-sectional diameter reduction in 3 of 7 ipsilateral vascular segments. At 40-60 mmHg, the diameter of only one segment was reduced. No changes were observed at 100-120 mmHg. Emboli prevented adequate perfusion of vascular segments in the absence of microfiltration. Median (interquartile range) neurologic score was reduced after SAH (sham, 27 (27); SAH 11 (7-17)). Deficits correlated with middle cerebral artery (MCA) diameter and SAH grade. MCA diameter also correlated with SAH grade. Only when utilizing microfiltration, controlling for hemorrhage size, and casting at perfusion pressures of 60-80 mmHg does India ink/gelatin vascular casting demonstrate consistent DCV that correspnds to neurological deficits. This allows measurement of both anatomical and clinical DCV in the mouse.
引用
收藏
页码:510 / 516
页数:7
相关论文
共 17 条
[1]   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
[2]  
CRAWLEY J, 2000, WHATS WRONG MY MOUSE, V1, P31
[3]   Molecular keys to the problems of cerebral vasospasm [J].
Dietrich, HH ;
Dacey, RG Jr .
NEUROSURGERY, 2000, 46 (03) :517-530
[4]   RELATION OF CEREBRAL VASOSPASM TO SUBARACHNOID HEMORRHAGE VISUALIZED BY COMPUTERIZED TOMOGRAPHIC SCANNING [J].
FISHER, CM ;
KISTLER, JP ;
DAVIS, JM .
NEUROSURGERY, 1980, 6 (01) :1-9
[5]   NEUROLOGICAL DEFICIT AND EXTENT OF NEURONAL NECROSIS ATTRIBUTABLE TO MIDDLE CEREBRAL-ARTERY OCCLUSION IN RATS - STATISTICAL VALIDATION [J].
GARCIA, JH ;
WAGNER, S ;
LIU, KF ;
HU, XJ .
STROKE, 1995, 26 (04) :627-634
[6]   PREDICTION OF DELAYED NEUROLOGICAL DEFICIT AFTER SUBARACHNOID HEMORRHAGE - A CT BLOOD LOAD AND DOPPLER VELOCITY APPROACH [J].
GROSSET, DG ;
MCDONALD, I ;
COCKBURN, M ;
STRAITON, J ;
BULLOCK, RR .
NEURORADIOLOGY, 1994, 36 (06) :418-421
[7]   EFFECTS OF CEREBRAL-ISCHEMIA IN MICE DEFICIENT IN NEURONAL NITRIC-OXIDE SYNTHASE [J].
HUANG, ZH ;
HUANG, PL ;
PANAHIAN, N ;
DALKARA, T ;
FISHMAN, MC ;
MOSKOWITZ, MA .
SCIENCE, 1994, 265 (5180) :1883-1885
[8]   TRANSIENT APPEARANCE OF NO-REFLOW PHENOMENON IN MONGOLIAN GERBILS [J].
ITO, U ;
OHNO, K ;
YAMAGUCHI, T ;
TOMITA, H ;
INABA, Y ;
KASHIMA, M .
STROKE, 1980, 11 (05) :517-521
[9]   Amelioration of vasospasm after subarachnoid hemorrhage in transgenic mice overexpressing CuZn-superoxide dismutase [J].
Kamii, H ;
Kato, I ;
Kinouchi, H ;
Chan, PH ;
Epstein, CJ ;
Akabane, A ;
Okamoto, H ;
Yoshimoto, T .
STROKE, 1999, 30 (04) :867-871
[10]   Systemic administration of the potassium channel activator cromakalim attenuates cerebral vasospasm after experimental subarachnoid hemorrhage [J].
Kwan, AL ;
Lin, CL ;
Yanamoto, H ;
Howng, SL ;
Kassell, NF ;
Lee, KS .
NEUROSURGERY, 1998, 42 (02) :347-350