Induction of anxiety-like behavior in mice during the initial stages of infection with the agent of murine colonic hyperplasia Citrobacter rodentium

被引:268
作者
Lyte, Mark
Li, Wang
Opitz, Noel
Gaykema, Ronald P. A.
Goehler, Lisa E.
机构
[1] Texas Tech Univ, Hlth Sci Ctr, Dept Pharm Practice, Sch Pharm, Lubbock, TX 79430 USA
[2] Minneapolis Med Res Fdn Inc, Minneapolis, MN 55404 USA
[3] Univ Minnesota, Dept Vet & Biomed Sci, St Paul, MN 55108 USA
[4] Univ Virginia, Dept Psychol, Charlottesville, VA 22904 USA
基金
美国国家卫生研究院;
关键词
inflammatory bowel disease; infection; behavior; Citrobacter rodentium;
D O I
10.1016/j.physbeh.2006.06.019
中图分类号
B84 [心理学];
学科分类号
04 ; 0402 ;
摘要
Symptoms of anxiety frequently occur concomitant to the development and persistence of inflammatory bowel disease (IBD) in patients. In the present study, we utilized an animal model of IBD, infection with Citrobacter rodentium, to determine whether the infection per se can drive anxiety-like behavior. Nine-week-old CF-1 male mice were challenged orally with either saline or C. rodentium. Early in the infective process (7-8 h later), mice were tested on a hole-board open field apparatus for anxiety-like behavior measurement. Immediately following behavioral testing, plasma samples were obtained for immune cytokine analysis and colons were excised for histological analysis. In additional animals, vagal ganglia were removed and processed for c-Fos protein detection. Challenge with C. rodentium significantly increased anxiety-like behavior as evidenced by avoidance of the center area and increased risk assessment behavior. Plasma levels of the cytokines IFN-gamma, TNF-alpha and IL-12 were not different. However vagal sensory ganglia from C. rodentium-treated animals evinced significantly more c-Fos protein-positive neurons, consistent with vagal afferent transmission of C. rodentium-related signals from gut to brain. Histological examination of the colon indicated a lack of overt inflammation at the 8 h post-challenge time point, indicating that the differences in behavior were unlikely to follow from inflammation-related stress. The results of the present study demonstrate that infection with C. rodentium can induce anxiety-like symptoms that are likely mediated via vagal sensory neurons. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:350 / 357
页数:8
相关论文
共 61 条
[1]  
Addolorato G, 1996, HEPATO-GASTROENTEROL, V43, P1513
[2]  
Anisman H, 1999, ADV EXP MED BIOL, V461, P199
[3]   Sickness behavior of rats with abdominal sepsis can be improved by antibiotic and G-CSF prophylaxis in clinic modeling randomized trials [J].
Bauhofer, A ;
Schwarting, RKW ;
Köster, M ;
Schmitt, A ;
Lorenz, W ;
Pawlak, CR .
INFLAMMATION RESEARCH, 2004, 53 (12) :697-705
[4]   Ascending visceral regulation of cortical affective information processing [J].
Berntson, GG ;
Sarter, M ;
Cacioppo, JT .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2003, 18 (08) :2103-2109
[5]   THE ROLE OF ANXIETY AND DEPRESSION IN THE IRRITABLE-BOWEL-SYNDROME [J].
BLANCHARD, EB ;
SCHARFF, L ;
SCHWARZ, SP ;
SULS, JM ;
BARLOW, DH .
BEHAVIOUR RESEARCH AND THERAPY, 1990, 28 (05) :401-405
[6]   EFFECTS OF INTERLEUKIN-1 RECEPTOR ANTAGONIST ON THE BEHAVIORAL-EFFECTS OF LIPOPOLYSACCHARIDE IN RAT [J].
BLUTHE, RM ;
DANTZER, R ;
KELLEY, KW .
BRAIN RESEARCH, 1992, 573 (02) :318-320
[7]   Central injection of interleukin-13 potentiates LPS-induced sickness behavior in rats [J].
Bluthé, RM ;
Bristow, A ;
Lestage, J ;
Imbs, C ;
Dantzer, R .
NEUROREPORT, 2001, 12 (18) :3979-3983
[8]   Psychosocial aspects of inflammatory bowel disease [J].
Casati, J ;
Toner, BB .
BIOMEDICINE & PHARMACOTHERAPY, 2000, 54 (07) :388-393
[9]   Social learning, affective state and passive coping in irritable bowel syndrome and inflammatory bowel disease [J].
Crane, C ;
Martin, M .
GENERAL HOSPITAL PSYCHIATRY, 2004, 26 (01) :50-58
[10]   EspJ is a prophage-carried type III effector protein of attaching and effacing pathogens that modulates infection dynamics [J].
Dahan, S ;
Wiles, S ;
La Ragione, RM ;
Best, A ;
Woodward, MJ ;
Stevens, MP ;
Shaw, RK ;
Chong, YW ;
Knutton, S ;
Phillips, A ;
Frankel, G .
INFECTION AND IMMUNITY, 2005, 73 (02) :679-686