Further characterisation of a thromboembolic model of stroke in the rat

被引:19
作者
Beech, JS
Williams, SCR
Campbell, CA
Bath, PMW
Parsons, AA
Hunter, AJ
Menon, DK
机构
[1] Univ Cambridge, Addenbrookes Hosp, Dept Med, Div Anaesthesia, Cambridge CB2 2QQ, England
[2] Inst Psychiat, London SE5 8AF, England
[3] Smithkline Beecham, Neurosci Res, Harlow CM19 5AW, Essex, England
[4] Univ Nottingham, Div Stroke Med, Nottingham NG5 1PB, England
基金
英国医学研究理事会;
关键词
ischaemia; magnetic resonance imaging; thromboemolic stroke; models;
D O I
10.1016/S0006-8993(00)03331-X
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We have used magnetic resonance imaging (MRI) techniques to characterise a rat model of thromboembolic stroke. The consequences of acute perfusion deficit associated with a middle cerebral artery occlusion (MCAo) by a newly formed thrombus was mapped by interrogation of the tissue oxygenation status using gradient echo methods and production of T2* maps. Final infarct size was subsequently assessed at 24-h post-ischaemia by histology with 2,3,5-triphenyltetrazolium chloride (TTC) staining. Animals displayed an infarct volume of 178.7 +/- 84.2 mm(3) (mean +/-S.D.) with a large coefficient of variation (47%) and range of values (85.6-265.5 mm(3)). This variability provided us with an opportunity to assess the relationships between early imaging observations and eventual infarct size. For a single cerebral slice, at the centre of the MCA territory, a relationship between the area of reduced T2* at 1 and 2 h post MCAo correlated highly with final lesion area (Spearman rank correlation, r=0.98. P<0.01. n=9). Lesion volumes in the thromboembolic MCAo model were compared with a 120-min occlusion. 22-h reperfusion protocol using an intraluminal thread MCAo approach. For the thromboembolic model. the total lesion volume was found to be smaller (178.7<plus/minus>84.2 vs. 243.3 +/- 50.1 mm(3), mean +/-S.D., Student's t-test P=0.046) and showed a greater variability (coefficient of variations: 47% vs. 21%). These data underline the relative variability of this embolic model and provide important preliminary information regarding the value of early changes in T2* in predicting eventual infarct size. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:18 / 24
页数:7
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