Meddings J B, Swain M G
Gastrointestinal Research Group, University of Calgary, Alberta, Canada.
Gastroenterology. 2000 Oct;119(4):1019-28. doi: 10.1053/gast.2000.18152.
BACKGROUND & AIMS: Abnormal presentation of luminal constituents to the mucosal immune system, caused by dysfunction of the intestinal epithelial barrier, is a candidate theory for the cause of Crohn's disease. Increased epithelial permeability is found in subgroups of patients at high risk for the development of Crohn's disease and has been found to precede disease recurrence. Clinical observations have suggested that disease recurrence can follow times of increased psychological stress, although the underlying mechanism remains obscure. We hypothesized that environmental stress increases gastrointestinal permeability.
We evaluated site-specific gastrointestinal permeability after application of graded levels of stress in rats.
Increased epithelial permeability after stress was shown in all regions of the gastrointestinal tract and seemed to be mediated by adrenal corticosteroids. Stress-induced increases in epithelial permeability disappeared after adrenalectomy or pharmacologic blockade of glucocorticoid receptors. Dexamethasone treatment of control animals increased gastrointestinal permeability and mimicked the effects of stress.
Psychological stress may increase gastrointestinal permeability, allowing luminal constituents access to the mucosal immune system. This provides a potential mechanism for the observation of stress-induced disease recurrence in Crohn's disease.
肠上皮屏障功能障碍导致管腔成分向黏膜免疫系统的异常呈递,是克罗恩病病因的一种候选理论。在患克罗恩病高风险的患者亚组中发现上皮通透性增加,且已发现其先于疾病复发。临床观察表明,疾病复发可在心理压力增加之后出现,尽管潜在机制仍不清楚。我们推测环境压力会增加胃肠道通透性。
我们在给大鼠施加不同程度的压力后,评估特定部位的胃肠道通透性。
应激后胃肠道所有区域的上皮通透性均增加,且似乎由肾上腺皮质激素介导。肾上腺切除或糖皮质激素受体的药物阻断后,应激诱导的上皮通透性增加消失。地塞米松治疗对照动物增加了胃肠道通透性,并模拟了应激的作用。
心理压力可能增加胃肠道通透性,使管腔成分接触黏膜免疫系统。这为观察到克罗恩病中应激诱导的疾病复发提供了一种潜在机制。