Behavioral Deficits After Distal Focal Cerebral Ischemia in Mice: Usefulness of Adhesive Removal Test

被引:88
作者
Freret, Thomas [1 ,2 ]
Bouet, Valentine [1 ,2 ]
Leconte, Claire [1 ,2 ]
Roussel, Simon [2 ]
Chazalviel, Laurent [2 ]
Divoux, Didier [2 ]
Schumann-Bard, Pascale [1 ,2 ]
Boulouard, Michel [1 ]
机构
[1] Univ Caen, Grp Memoire & Plasticite Comportementale, UFR Sci Pharmaceut, UPRES EA 4259, F-14032 Caen, France
[2] Univ Paris 05, Univ Caen Basse Normandie,UMR 6232, CERVOxy Team Hypoxia & Cerebrovasc Pathophysiol, Unite Mixte Rech CEA,CNRS,CI NAPS, Caen, France
关键词
sticky label test; stroke; functional recovery; sensorimotor deficits; MOTOR CORTEX STROKE; FUNCTIONAL RECOVERY; ARTERY OCCLUSION; STAIRCASE TEST; MUS-MUSCULUS; END-POINT; RATS; SENSORIMOTOR; BRAIN; MOUSE;
D O I
10.1037/a0014157
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Distal occlusion of the middle cerebral artery (dMCAo), which closely mimics human stroke, is one of the most used animal models. However, although assessment of histological and functional outcome is increasingly recommended for preclinical studies, the latter is often excluded because of the high difficulties to estimate, especially in mice, behavioral impairments. The aim of our study was to deeply screen functional consequences of distal permanent MCAo in mice to target relevant behaviors for future studies. A set of sensorimotor and cognitive tests were performed during 3 weeks postsurgery in 2 groups of mice. Afterward, brain infarctions were estimated by histological staining or magnetic resonance imaging. Overall, while no long-term functional impairments could be detected, the adhesive removal was the only test showing a deficit. Interestingly, this sensorimotor impairment was correlated to cortical damage 3 weeks after surgery. In conclusion, despite the fact that dMCAo-induced deficits could not be evidenced by most of our behavioral tests, the authors showed that the adhesive removal test was the only one, sensitive enough, to highlight a long-term deficit. This result suggests therefore that this mouse model of ischemia is relevant to efficiently assess therapeutic strategies with histological but also behavioral analysis, provided that relevant tests are used.
引用
收藏
页码:224 / 230
页数:7
相关论文
共 48 条
[41]   Sensorimotor impairments in Wistar Kyoto rats with cerebral infarction, induced by unilateral occlusion of the middle cerebral artery: Recovery of function [J].
vanderStaay, FJ ;
Augstein, KH ;
Horvath, E .
BRAIN RESEARCH, 1996, 715 (1-2) :180-188
[42]   EFFECT OF LACTACIDOSIS ON PYRIDINE-NUCLEOTIDE STABILITY DURING ISCHEMIA IN MOUSE-BRAIN [J].
WELSH, FA ;
SAKAMOTO, T ;
MCKEE, AE ;
SIMS, RE .
JOURNAL OF NEUROCHEMISTRY, 1987, 49 (03) :846-851
[43]   PROXIMAL AND DISTAL IMPAIRMENTS IN RAT FORELIMB USE IN REACHING FOLLOW UNILATERAL PYRAMIDAL TRACT LESIONS [J].
WHISHAW, IQ ;
PELLIS, SM ;
GORNY, B ;
KOLB, B ;
TETZLAFF, W .
BEHAVIOURAL BRAIN RESEARCH, 1993, 56 (01) :59-76
[44]   THE IMPAIRMENTS IN REACHING AND THE MOVEMENTS OF COMPENSATION IN RATS WITH MOTOR CORTEX LESIONS - AN END-POINT, VIDEORECORDING, AND MOVEMENT NOTATION ANALYSIS [J].
WHISHAW, IQ ;
PELLIS, SM ;
GORNY, BP ;
PELLIS, VC .
BEHAVIOURAL BRAIN RESEARCH, 1991, 42 (01) :77-91
[45]   An endpoint, descriptive, and kinematic comparison of skilled reaching in mice (Mus musculus) with rats (Rattus norvegicus) [J].
Whishaw, IQ .
BEHAVIOURAL BRAIN RESEARCH, 1996, 78 (02) :101-111
[46]   Dysexecutive syndrome after mild cerebral ischemia? Mice learn normally but have deficits in strategy switching [J].
Winter, B ;
Bert, B ;
Fink, H ;
Dirnagl, U ;
Endres, M .
STROKE, 2004, 35 (01) :191-195
[47]   Spatial cognitive performance after chronic focal cerebral ischemia in rats [J].
Yonemori, F ;
Yamaguchi, T ;
Yamada, H ;
Tamura, A .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1999, 19 (05) :483-494
[48]   A test for detecting long-term sensorimotor dysfunction in the mouse after focal cerebral ischemia [J].
Zhang, L ;
Schallert, T ;
Zhang, ZG ;
Jiang, Q ;
Arniego, P ;
Li, QJ ;
Lu, M ;
Chopp, M .
JOURNAL OF NEUROSCIENCE METHODS, 2002, 117 (02) :207-214