Teitelbaum Aaron A, Gareau Mélanie G, Jury Jennifer, Yang Ping Chang, Perdue Mary H
Intestinal Disease Research Program, Department of Pathology & Molecular Medicine, McMaster University, Hamilton, Ontario, Canada.
Am J Physiol Gastrointest Liver Physiol. 2008 Sep;295(3):G452-9. doi: 10.1152/ajpgi.90210.2008. Epub 2008 Jul 17.
Chronic psychological stress causes intestinal barrier dysfunction and impairs host defense mechanisms mediated by corticotrophin-releasing factor (CRF) and mast cells; however, the exact pathways involved are unclear. Here we investigated the effect of chronic CRF administration on colonic permeability and ion transport functions in rats and the role of mast cells in maintaining the abnormalities. CRF was delivered over 12 days via osmotic minipumps implanted subcutaneously in wild-type (+/+) and mast cell-deficient (Ws/Ws) rats. Colonic segments were excised for ex vivo functional studies in Ussing chambers [short-circuit current (Isc), conductance (G), and macromolecular permeability (horseradish peroxidase flux)], and analysis of morphological changes (mast cell numbers and bacterial host-interactions) was determined by light and electron microscopy. Chronic CRF treatment resulted in colonic mucosal dysfunction with increased Isc, G, and horseradish peroxidase flux in+/+but not in Ws/Ws rats. Furthermore, CRF administration caused mast cell hyperplasia and abnormal bacterial attachment and/or penetration into the mucosa only in+/+rats. Finally, selective CRF agonist/antagonist studies revealed that stimulation of CRF-R1 and CRF-R2 receptors induced the elevated secretory state and permeability dysfunction, respectively. Chronic CRF causes colonic barrier dysfunction in rats, which is mediated, at least in part, via mast cells. This information may be useful in designing novel treatment strategies for stress-related gastrointestinal disorders.
慢性心理应激会导致肠道屏障功能障碍,并损害由促肾上腺皮质激素释放因子(CRF)和肥大细胞介导的宿主防御机制;然而,其中的确切途径尚不清楚。在此,我们研究了慢性给予CRF对大鼠结肠通透性和离子转运功能的影响,以及肥大细胞在维持这些异常中的作用。通过皮下植入渗透微型泵,在野生型(+/+)和肥大细胞缺陷型(Ws/Ws)大鼠中持续12天给予CRF。切除结肠段,在尤斯灌流小室中进行离体功能研究[短路电流(Isc)、电导(G)和大分子通透性(辣根过氧化物酶通量)],并通过光学和电子显微镜确定形态学变化(肥大细胞数量和细菌与宿主的相互作用)。慢性CRF治疗导致+/+大鼠结肠黏膜功能障碍,表现为Isc、G和辣根过氧化物酶通量增加,而Ws/Ws大鼠未出现此现象。此外,给予CRF仅在+/+大鼠中导致肥大细胞增生以及细菌异常附着和/或侵入黏膜。最后,选择性CRF激动剂/拮抗剂研究表明,刺激CRF-R1和CRF-R2受体分别诱导分泌状态升高和通透性功能障碍。慢性CRF导致大鼠结肠屏障功能障碍,这至少部分是通过肥大细胞介导的。这些信息可能有助于设计针对应激相关胃肠道疾病的新型治疗策略。