Keep warm and get success: The role of postischemic temperature in the mouse middle cerebral artery occlusion model

被引:15
作者
Wu, Li [1 ]
Xu, Lili [1 ]
Xu, Xiaohui [1 ]
Fan, Xinying [1 ]
Xie, Yi [1 ]
Yang, Lian [1 ]
Lan, Wenya [1 ]
Zhu, Juehua [1 ]
Xu, Gelin [1 ]
Dai, Jianwu [2 ]
Jiang, Yongjun [1 ]
Liu, Xinfeng [1 ]
机构
[1] Nanjing Univ, Sch Med, Jinling Hosp, Dept Neurol, Nanjing 210008, Jiangsu, Peoples R China
[2] Chinese Acad Sci, Inst Genet & Dev Biol, Key Lab Mol Dev Biol, Beijing, Peoples R China
基金
美国国家科学基金会;
关键词
Stroke; Middle cerebral artery occlusion; Body temperature; Hypothermia; Success rate; Infarct volume; MILD HYPOTHERMIA; INFARCT VOLUME; GENE-EXPRESSION; ISCHEMIA; HYPERTHERMIA; NEUROPROTECTION; STROKE;
D O I
10.1016/j.brainresbull.2013.12.003
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Intraluminal suture middle cerebral artery occlusion (MCAO) model is the most frequently used model for ischemic stroke. However, the success rate of this model is variable among different research studies. This study aimed to investigate the effect of postischemic temperature on the success rate. A total of 100 C57BL/6 mice were randomized into two groups: control group (n=50), body temperature was allowed to self-regulate after MCAO; temperature-controlled group (n=50), mice were kept warm in an incubator for 12 h after MCAO. The body temperature of animals was measured before, during, and for 12 h after MCAO. Neurological deficits and infarct volumes were measured at 24 h after MCAO. There was significant difference (P<0.05) of the body temperature between the two groups from 0.5 h to 3.5 h post ischemia. Moreover, there was obvious difference between the success rates of the two groups (control group: 52%, temperature-controlled group: 84%, P<0.05). In the successful models, infarct volume was significantly (P<0.05) higher in temperature-controlled group (53.44% 9.83%, n=42) than control group (45.63% 10.24%, n=26). There was significant difference of the modified neurological severity scores (P<0.05), left adhesive tests (P<0.05) between the two groups. Our data demonstrated that postischemic warming contributed to the success of mouse MCAO model. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:12 / 17
页数:6
相关论文
共 35 条
[1]   Intra-Arterial Therapy for Acute Ischemic Stroke [J].
Abou-Chebl, Alex .
INTERVENTIONAL NEUROLOGY, 2012, 1 (02) :100-108
[2]   Hyperthermia up-regulates matrix metalloproteinases and accelerates basement membrane degradation in experimental stroke [J].
Alam, Mustafa ;
Mohammad, Askar ;
Rahman, Shakib ;
Todd, Kathryn ;
Shuaib, Ashfaq .
NEUROSCIENCE LETTERS, 2011, 495 (02) :135-139
[3]   Intraluminal Middle Cerebral Artery Occlusion (MCAO) Model for Ischemic Stroke with Laser Doppler Flowmetry Guidance in Mice [J].
Ansari, Saeed ;
Azari, Hassan ;
McConnell, Douglas J. ;
Afzal, Aqeela ;
Mocco, J. .
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS, 2011, (51)
[4]   Temperature-regulated model of focal ischemia in the mouse - A study with histopathological and behavioral outcomes [J].
Barber, PA ;
Hoyte, L ;
Colbourne, F ;
Buchan, AM .
STROKE, 2004, 35 (07) :1720-1725
[5]   Middle cerebral artery occlusion in the mouse by intraluminal suture coated with poly-L-lysine: neurological and histological validation [J].
Belayev, L ;
Busto, R ;
Zhao, WZ ;
Femandez, G ;
Ginsberg, MD .
BRAIN RESEARCH, 1999, 833 (02) :181-190
[6]   EFFECT OF MILD HYPOTHERMIA ON ISCHEMIA-INDUCED RELEASE OF NEUROTRANSMITTERS AND FREE FATTY-ACIDS IN RAT-BRAIN [J].
BUSTO, R ;
GLOBUS, MY ;
DIETRICH, WD ;
MARTINEZ, E ;
VALDES, I ;
GINSBERG, MD .
STROKE, 1989, 20 (07) :904-910
[7]  
Carmichael S Thomas, 2005, NeuroRx, V2, P396
[8]   The dual role of the neuroinflammatory response after ischemic stroke: modulatory effects of hypothermia [J].
Ceulemans, An-Gaelle ;
Zgavc, Tine ;
Kooijman, Ron ;
Hachimi-Idrissi, Said ;
Sarre, Sophie ;
Michotte, Yvette .
JOURNAL OF NEUROINFLAMMATION, 2010, 7
[9]   BRAIN INFARCTION IS NOT REDUCED IN SOD-1 TRANSGENIC MICE AFTER A PERMANENT FOCAL CEREBRAL-ISCHEMIA [J].
CHAN, PH ;
KAMII, H ;
YANG, GY ;
GAFNI, J ;
EPSTEIN, CJ ;
CARLSON, E ;
REOLA, L .
NEUROREPORT, 1993, 5 (03) :293-296
[10]   Therapeutic benefit of intravenous administration of bone marrow stromal cells after cerebral ischemia in rats [J].
Chen, JL ;
Li, Y ;
Wang, L ;
Zhang, ZG ;
Lu, DY ;
Lu, M ;
Chopp, M .
STROKE, 2001, 32 (04) :1005-1011