Laboratory of Pharmacology, Faculty of Medicine, Laboratory of Pharmacology, Democritus University of Thrace (DUTH), DUTH, Dragana, Alexandroupolis 68100, Thrace, Greece.
Drug Discov Today. 2009 Jul;14(13-14):713-20. doi: 10.1016/j.drudis.2009.04.002. Epub 2009 Apr 18.
Mounting evidence suggests that stress is implicated in the development of inflammatory bowel disease (IBD), via initial nervous disturbance and subsequent immune dysfunction through brain-gut interactions. The corticotropin-releasing factor (CRF) system, being the principal neuroendocrine coordinator of stress responses, is involved in the inflammatory process within the gastrointestinal tract, via vagal and peripheral pathways, as implied by multiple reports reviewed here. Blocking of CRF receptors could theoretically exert beneficial anti-inflammatory effects in colonic tissues. The recently synthesised small-molecule CRF(1) antagonists or alternatively non-peptide CRF(2) antagonists when available, may become new reliable options in the treatment of IBD.
越来越多的证据表明,压力通过初始的神经紊乱和随后的通过脑-肠相互作用的免疫功能障碍,与炎症性肠病(IBD)的发展有关。这里综述的多项报告表明,促肾上腺皮质释放因子(CRF)系统作为应激反应的主要神经内分泌协调者,通过迷走神经和外周途径参与胃肠道的炎症过程。CRF 受体的阻断理论上可以在结肠组织中发挥有益的抗炎作用。最近合成的小分子 CRF(1)拮抗剂或可用的非肽 CRF(2)拮抗剂,可能成为 IBD 治疗的新的可靠选择。