Cortical devascularization: quantitative diffusion weighted magnetic resonance imaging and histological findings

被引:13
作者
Bartnik, BL
Kendall, EJ
Obenaus, A
机构
[1] Univ Saskatchewan, Coll Med, Dept Anat & Cell Biol, Saskatoon, SK S7N 5E5, Canada
[2] Univ Saskatchewan, Coll Med, Acad Dept Med Imaging, Saskatoon, SK S7N 0W8, Canada
[3] Loma Linda Univ, Dept Radiat Med, Radiobiol Program, Loma Linda, CA 92354 USA
关键词
cortical devascularization; ischemia; rat; traumatic brain injury; diaschisis;
D O I
10.1016/S0006-8993(01)02805-0
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
This study investigates the development of a small focal cortical lesion produced in a model of brain injury. Two approaches were chosen: diffusion weighted magnetic resonance imaging (DWI) and histology. DW images were collected before devascularization and at 0.5, 1, 2, 3, 5, 7 and 14 days after treatment. Apparent diffusion coefficient (ADC) maps were calculated from the DW images to quantify lesion development. As a second measure of injury, tissue morphology was analyzed using cresyl violet histochemistry. A significant reduction in ADC values within the cortex below the injury site by 0.5 days after surgery was observed. Between 5 and 14 days the ADC values recovered to control levels. ADC changes were also observed in the contralateral cortex at 0.5, 1 and 5 days. The decrease in ADC observed at the early time points suggested cytotoxic edema, whereas the recovery to control levels at later time points suggested infarct formation. This model of brain injury resulted in progressive but relatively slow formation of a pan-necrotic infarct within 14 days. In particular, substantial amounts of cell death were not observed until 2 days after surgery.. Overall, the quantitative and histological measures of this lesion are consistent with those observed for an ischemic type of injury, however, the time course of these lesions' development are consistent with other models of traumatic brain injury. Our data demonstrates that DWI is a highly sensitive metric for ischemic-type damage that results from brain injury. (C) 2001 Elsevier Science BY. All rights reserved.
引用
收藏
页码:133 / 142
页数:10
相关论文
共 45 条
[1]   Diffusion and high resolution MRI of traumatic brain injury in rats: Time course and correlation with histology [J].
Albensi, BC ;
Knoblach, SM ;
Chew, BGM ;
O'Reilly, MP ;
Faden, AI ;
Pekar, JJ .
EXPERIMENTAL NEUROLOGY, 2000, 162 (01) :61-72
[2]   Detection of acute pathologic changes following experimental traumatic brain injury using diffusion-weighted magnetic resonance imaging [J].
Alsop, DC ;
Murai, H ;
Detre, JA ;
McIntosh, TK ;
Smith, DH .
JOURNAL OF NEUROTRAUMA, 1996, 13 (09) :515-521
[3]   TRANSHEMISPHERIC DIASCHISIS - A REVIEW AND COMMENT [J].
ANDREWS, RJ .
STROKE, 1991, 22 (07) :943-949
[4]  
[Anonymous], RAT BRAIN STEREOTAXI
[5]   Diffusion anisotropy measurements in ischaemic stroke of the human brain [J].
Armitage, P. A. ;
Bastin, M. E. ;
Marshall, I. ;
Wardlaw, J. M. ;
Cannon, J. .
MAGNETIC RESONANCE MATERIALS IN PHYSICS BIOLOGY AND MEDICINE, 1998, 6 (01) :28-36
[6]   Diffusion- and T-2-weighted MRI of closed-head injury in rats: A time course study and correlation with histology [J].
Assaf, Y ;
BeitYannai, E ;
Shohami, E ;
Berman, E ;
Cohen, Y .
MAGNETIC RESONANCE IMAGING, 1997, 15 (01) :77-85
[7]   Contribution of vasogenic and cellular edema to traumatic brain swelling measured by diffusion-weighted imaging [J].
Barzo, P ;
Marmarou, A ;
Fatouros, P ;
Hayasaki, K ;
Corwin, F .
JOURNAL OF NEUROSURGERY, 1997, 87 (06) :900-907
[8]   MECHANISM OF DETECTION OF ACUTE CEREBRAL-ISCHEMIA IN RATS BY DIFFUSION-WEIGHTED MAGNETIC-RESONANCE MICROSCOPY [J].
BENVENISTE, H ;
HEDLUND, LW ;
JOHNSON, GA .
STROKE, 1992, 23 (05) :746-754
[9]   Colony stimulating factor-1 potentiates neuronal survival in cerebral cortex ischemic lesion [J].
Berezovskaya, O ;
Maysinger, D ;
Fedoroff, S .
ACTA NEUROPATHOLOGICA, 1996, 92 (05) :479-486
[10]   DIFFUSION-WEIGHTED IMAGING STUDIES OF CEREBRAL-ISCHEMIA IN GERBILS - POTENTIAL RELEVANCE TO ENERGY FAILURE [J].
BUSZA, AL ;
ALLEN, KL ;
KING, MD ;
VANBRUGGEN, N ;
WILLIAMS, SR ;
GADIAN, DG .
STROKE, 1992, 23 (11) :1602-1612