Chronic psychosocial stress induces visceral hyperalgesia in mice

被引:56
作者
Tramullas, Monica [2 ]
Dinan, Timothy G. [2 ,3 ]
Cryan, John F. [1 ,2 ]
机构
[1] Natl Univ Ireland Univ Coll Cork, Dept Anat, Coll Rd, Cork, Ireland
[2] Natl Univ Ireland Univ Coll Cork, Alimentary Pharmabiot Ctr, Cork, Ireland
[3] Natl Univ Ireland Univ Coll Cork, Dept Psychiat, Cork, Ireland
来源
STRESS-THE INTERNATIONAL JOURNAL ON THE BIOLOGY OF STRESS | 2012年 / 15卷 / 03期
关键词
Brain-gut axis; chronic stress; colorectal distension; social avoidance; somatic analgesia; visceral hypersensitivity; IRRITABLE-BOWEL-SYNDROME; PSEUDO-AFFECTIVE RESPONSES; FUNCTIONAL GI-DISORDERS; SOCIAL DEFEAT STRESS; DSS-INDUCED COLITIS; BRAIN-GUT AXIS; COLORECTAL DISTENSION; ANIMAL-MODELS; COLONIC INFLAMMATION; MATERNAL SEPARATION;
D O I
10.3109/10253890.2011.622816
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
Experimental and clinical evidence has shown that chronic stress plays an important role in the onset and/or exacerbation of symptoms of functional gastrointestinal disorders. Here, we aimed to investigate whether exposure to a chronic and temporally unpredictable psychosocial stressor alters visceral and somatic nociception as well as anxiety-related behaviour. In male C57BL/6J mice, chronic stress was induced by repeated exposure to social defeat (SD, 2 h) and overcrowding (OC, 24 h) during 19 consecutive days. Visceral and somatic nociception was evaluated by colorectal distension and a hot plate, respectively. The social interaction test was used to assess social anxiety. Mice exposed to psychosocial stress developed visceral hyperalgesia and somatic hypoalgesia 24 h following the last stress session. SD/OC mice also exhibited social anxiety-like behaviour. All these changes were also associated with physiological alterations, measured as a decreased faecal pellet output and hypothalamic-pituitary-adrenal (HPA) axis disruption. Taken together, these data confirm that this mouse model of chronic psychosocial stress may be useful for studies on the pathophysiological mechanisms underlying such stress-associated disorders and to further test potential therapies.
引用
收藏
页码:281 / 292
页数:12
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