Sleep deprivation worsens inflammation and delays recovery in a mouse model of colitis

被引:118
作者
Tang, Yueming [1 ]
Preuss, Fabian [1 ,4 ]
Turek, Fred W. [4 ]
Jakate, Shriram [3 ]
Keshavarzian, Ali [1 ,2 ]
机构
[1] Rush Univ, Dept Internal Med, Div Digest Dis & Nutr, Med Ctr, Chicago, IL 60612 USA
[2] Rush Univ, Dept Pharmacol & Mol Biophys & Physiol, Med Ctr, Chicago, IL 60612 USA
[3] Rush Univ, Dept Pathol, Med Ctr, Chicago, IL 60612 USA
[4] Northwestern Univ, Ctr Sleep & Circadian Biol, Dept Neurobiol & Physiol, Evanston, IL 60208 USA
关键词
Inflammatory bowel disease; Sleep deprivation; Dextran sodium sulfate; Colitis; Myeloperoxidase; Sleep disturbance; BOWEL-DISEASE; ULCERATIVE-COLITIS; PSYCHOLOGICAL STRESS; CROHNS-DISEASE; IBD; DISTURBANCES; MECHANISMS; CYTOKINES; INSOMNIA; HUMANS;
D O I
10.1016/j.sleep.2008.12.009
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and aim: We recently showed that patients with inflammatory bowel disease (IBD) report significantly more sleep disturbances. To determine whether disrupted sleep can affect the severity of inflammation and the course of IBD, we used an animal model of colonic inflammation to determine the effects of acute and chronic intermittent sleep deprivation on the severity of colonic inflammation and tissue damage in colitis and recovery from this damage. Methods: Acute sleep deprivation (ASD) consisted of 24 h of forced locomotor activity in a mechanical wheel rotating at a constant speed. Chronic intermittent sleep deprivation (CISD) consisted of an acute sleep deprivation episode, followed by additional sleep deprivation periods in the wheel for 6 h every other day throughout the 10 day study period. To induce colitis, mice were given 2% dextran sodium sulfate (DSS) in their daily drinking water for 7 days. The development and severity of colitis were monitored by measuring weight loss and tissue myeloperoxidase (MPO) activity daily and colon histology scores 10 days after initiation of colitis. Results: ASD or CISD did not cause colonic inflammation in vehicle-treated mice. Changes in daily body weight, tissue MPO levels and colon histopathology score were similar between mice that were sleep deprived and controls. Daily DSS ingestion caused colitis in mice. ASD worsened colonic inflammation: tissue MPO levels in ASD/DSS-treated mice were significantly higher than in DSS-treated mice that were not sleep deprived. However, the worsening of colonic inflammation by ASD was not enough to exacerbate clinical manifestations of colitis such as weight loss. In contrast, the deleterious effects of CISD were severe enough to cause worsening of histological and clinical manifestations of colitis. The deleterious effects of sleep deprivation on severity of colitis appeared to be due to both increased colonic inflammation and a decrease in the ability of mice to recover from DSS-induced colonic injury. Conclusion: Both acute and chronic intermittent sleep deprivation exacerbate colonic inflammation. Thus, sleep deprivation could be an environmental trigger that predisposes IBD patients to develop flare ups and a more severe disease course. These results provide a scientific rationale to conduct an interventional trial to determine whether improvement in sleep patterns will prevent IBD flare ups, modify the disease course, and improve quality of life. (c) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:597 / 603
页数:7
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