Deficits in novelty exploration after controlled cortical impact

被引:34
作者
Wagner, Amy K.
Postal, Brett A.
Darrah, Shaun D.
Chen, Xiangbai
Khan, Amina S.
机构
[1] Univ Pittsburgh, Dept Phys Med & Rehabil, Pittsburgh, PA 15260 USA
[2] Univ Pittsburgh, Safar Ctr Resuscitat Res, Pittsburgh, PA USA
关键词
exploratory behavior; novelty; open field; traumatic brain injury; Y-maze;
D O I
10.1089/neu.2007.0274
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Experimental models of traumatic brain injury (TBI) have been utilized to characterize the behavioral derangements associated with brain trauma. Several studies exist characterizing motor function in the controlled cortical impact (CCI) injury model of TBI, but less research has focused on how CCI affects exploratory behavior. The goal of this study was to characterize deficits in three novelty exploration tasks after the CCI. Under anesthesia, 37 adult male Sprague Dawley rats received CCI (2.7 mm and 2.9 mm; 4 m/sec) over the right parietal cortex or sham surgery. For days 1-6 post-surgery, the beam balance and beam walking tasks were used to assess motor deficits. The Open Field, Y-Maze, and Free Choice Novelty (FCN) tasks were used to measure exploratory deficits from days 7-14 post-surgery. Injured rats displayed a significant, but transient, deficit on each motor task (p < 0.0001). Open Field results showed that injured rats had lower activity levels than shams (p < 0.0001), displayed less habituation to the task, and had more anxiety related behaviors ( thigmotaxis) across days (p < 0.0001). Y-maze results suggest that injured rats spent less time in the novel arm versus the familiar arms when compared to shams (p < 0.0001). For FCN, injured rats were less active (p < 0.05) and spent less time and had fewer interactions with objects in the novel environment compared to shams (p < 0.05). These results suggest that several ethological factors contribute to exploratory deficits after CCI and can be effectively characterized with the behavioral tasks described. Future work will utilize these tasks to evaluate the neural substrates underlying exploratory deficits after TBI.
引用
收藏
页码:1308 / 1320
页数:13
相关论文
共 78 条
[1]   Motivational deficits after brain injury: A neuropsychological approach using new assessment techniques [J].
Al-Adawi, S ;
Powell, JH ;
Greenwood, RJ .
NEUROPSYCHOLOGY, 1998, 12 (01) :115-124
[2]   Attentional and processing skills following traumatic brain injury in early childhood [J].
Anderson, V ;
Catroppa, C ;
Morse, S ;
Haritou, F ;
Rosenfeld, J .
BRAIN INJURY, 2005, 19 (09) :699-710
[3]   INTRAVENTRICULAR NOREPINEPHRINE FACILITATES MOTOR RECOVERY FOLLOWING SENSORIMOTOR CORTEX INJURY [J].
BOYESON, MG ;
FEENEY, DM .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1990, 35 (03) :497-501
[4]   POSTTRAUMATIC BRAIN HYPOTHERMIA PROVIDES PROTECTION FROM SENSORIMOTOR AND COGNITIVE-BEHAVIORAL DEFICITS [J].
BRAMLETT, HM ;
GREEN, EJ ;
DIETRICH, WD ;
BUSTO, R ;
GLOBUS, MYT ;
GINSBERG, MD .
JOURNAL OF NEUROTRAUMA, 1995, 12 (03) :289-298
[5]   Hippocampally dependent and independent chronic spatial navigational deficits following parasagittal fluid percussion brain injury in the rat [J].
Bramlett, HM ;
Green, EJ ;
Dietrich, WD .
BRAIN RESEARCH, 1997, 762 (1-2) :195-202
[6]   Is dopamine required for natural reward? [J].
Cannon, CM ;
Bseikri, MR .
PHYSIOLOGY & BEHAVIOR, 2004, 81 (05) :741-748
[7]   Elevated cholecystokininergic tone constitutes an important molecular/neuronal mechanism for the expression of anxiety in the mouse [J].
Chen, Q ;
Nakajima, A ;
Meacham, C ;
Tang, YP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (10) :3881-3886
[8]   A detailed ethological analysis of the mouse open field test: effects of diazepam, chlordiazepoxide and an extremely low frequency pulsed magnetic field [J].
Choleris, E ;
Thomas, AW ;
Kavaliers, M ;
Prato, FS .
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 2001, 25 (03) :235-260
[9]  
COLBOURNE F, 1995, J NEUROSCI, V15, P7250
[10]   Tapered progesterone withdrawal enhances behavioral and molecular recovery after traumatic brain injury [J].
Cutler, SM ;
Pettus, EH ;
Hoffman, SW ;
Stein, DG .
EXPERIMENTAL NEUROLOGY, 2005, 195 (02) :423-429