Evaluation of cage leaving behaviour in rats as a free choice paradigm

被引:8
作者
Bert, B. [1 ]
Schmidt, N. [1 ]
Voigt, J. P. [2 ]
Fink, H. [1 ]
Rex, A. [3 ]
机构
[1] Free Univ Berlin, Sch Vet Med, Inst Pharmacol & Toxicol, D-14195 Berlin, Germany
[2] Univ Nottingham, Sch Vet Med & Sci, Loughborough LE12 5RD, Leics, England
[3] Charite, Ctr Stroke Res, Dept Neurol, D-10098 Berlin, Germany
关键词
Anxiolytic drugs; Free exploratory behaviour; Gender; Strain differences; Rat; Trait anxiety; ELEVATED PLUS-MAZE; FREE-EXPLORATORY PARADIGM; BENZODIAZEPINE-RECEPTOR LIGANDS; STRESS-INDUCED HYPERTHERMIA; SPRAGUE-DAWLEY RATS; ANIMAL-MODELS; TRAIT ANXIETY; PHARMACOLOGICAL VALIDATION; ANTICIPATORY ANXIETY; 5-HT1A RECEPTORS;
D O I
10.1016/j.vascn.2013.01.001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: The free exploratory paradigm is regarded as a reliable test for trait anxiety in mice but it may also be useful in rats. Previously, we showed that rat strains differ in their free exploration of novel areas, i.e. the surroundings of their familiar home cage when the lid was removed. Aim: Therefore, the purpose of the present study was to further examine strain, sex, and age differences in animals from different breeders in combination with pharmacological treatment designed to modify anxiety. Methods: In the present study free exploratory behaviour test was evaluated in Sprague Dawley and Wistar rats from different breeders. We assessed seasonal variation, habituation to the test, and the impact of gender and age on exploration. Furthermore, we monitored exploration following intraperitoneal diazepam, 8-OH-DPAT and caffeine administration. Parameters measured were latency to start exploring the outside of the cage, the percentage of rats that explored the outside, as well as the number of visits. Results: There was no seasonal variability in free exploratory behaviour. However, strains and sexes differed in the test results, though age-related differences had less impact. Diazepam (2 mg/kg) and 8-OH-DPAT (30, 100 and 300 mu g/kg) decreased neophobia while caffeine (50 mg/kg) increased the latency to explore the outside the next day. Discussion: The free exploratory behaviour test can be used as a simple and complementary test to study trait anxiety-related behaviour in rats. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:240 / 249
页数:10
相关论文
共 71 条
[1]   CIRCANNUAL CHANGES IN THE DURATION OF THE IMMOBILITY RESPONSE OF RATS IN THE FORCED SWIM TEST [J].
ABEL, EL .
PHYSIOLOGY & BEHAVIOR, 1995, 58 (03) :591-593
[2]   Serotonergic systems associated with arousal and vigilance behaviors following administration of anxiogenic drugs [J].
Abrams, JK ;
Johnson, PL ;
Hay-Schmidt, A ;
Mikkelsen, JD ;
Shekhar, A ;
Lowry, CA .
NEUROSCIENCE, 2005, 133 (04) :983-997
[3]  
Anderson EE, 1938, PEDAGOG SEMIN J GEN, V53, P335
[4]   Animal models: Trait or state measure? The test-retest reliability of the elevated plus-maze and behavioral despair [J].
Andreatini, R ;
Bacellar, LFS .
PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY, 2000, 24 (04) :549-560
[5]   CAFFEINE-INDUCED ANXIOGENESIS - THE ROLE OF ADENOSINE, BENZODIAZEPINE AND NORADRENERGIC RECEPTORS [J].
BALDWIN, HA ;
FILE, SE .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1989, 32 (01) :181-186
[6]   Measuring normal and pathological anxiety-like behaviour in mice: a review [J].
Belzung, C ;
Griebel, G .
BEHAVIOURAL BRAIN RESEARCH, 2001, 125 (1-2) :141-149
[7]   Further pharmacological validation of the BALB/c neophobia in the free exploratory paradigm as an animal model of trait anxiety [J].
Belzung, C ;
Berton, F .
BEHAVIOURAL PHARMACOLOGY, 1997, 8 (6-7) :541-548
[8]   PD135158, A CCK-B ANTAGONIST, REDUCES STATE, BUT NOT TRAIT ANXIETY IN MICE [J].
BELZUNG, C ;
PINEAU, N ;
BEUZEN, A ;
MISSLIN, R .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1994, 49 (02) :433-436
[9]   Pharmacologic alternatives to antidepressants in posttraumatic stress disorder: A systematic review [J].
Berger, William ;
Mendlowicz, Mauro V. ;
Marques-Portella, Carla ;
Kinrys, Gustavo ;
Fontenelle, Leonardo F. ;
Marmar, Charles R. ;
Figueira, Ivan .
PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY, 2009, 33 (02) :169-180
[10]   Mice over-expressing the 5-HT1A receptor in cortex and dentate gyrus display exaggerated locornotor and hypothermic response to 8-OH-DPAT [J].
Bert, B ;
Fink, H ;
Hörtnagl, H ;
Veh, RW ;
Davies, B ;
Theuring, F ;
Kusserow, H .
BEHAVIOURAL BRAIN RESEARCH, 2006, 167 (02) :328-341