Brzozowski Bartosz, Mazur-Bialy Agnieszka, Pajdo Robert, Kwiecien Slawomir, Bilski Jan, Zwolinska-Wcislo Malgorzata, Mach Tomasz, Brzozowski Tomasz
Department of Physiology, Jagiellonian University Medical College, 16 Grzegorzecka Street, 31-531 Cracow, Poland.
Curr Neuropharmacol. 2016;14(8):892-900. doi: 10.2174/1570159x14666160404124127.
Stress of different origin is known to alter so called "braingut axis" and contributes to a broad array of gastrointestinal disorders including inflammatory bowel disease (IBD), irritable bowel syndrome (IBS) and other functional gastrointestinal diseases. The stressful situations and various stressors including psychosocial events, heat, hypo- and hyperthermia may worsen the course of IBD via unknown mechanism. The aims of this paper were to provide an overview of experimental and clinical evidences that stress activates the brain-gut axis which results in a mucosal mast cells activation and an increase in the production of proinflammatory cytokines and other endocrine and humoral mediators.
Research and online content related to effects of stress on lower bowel disorders are reviewed and most important mechanisms are delineated.
Brain conveys the neural, endocrine and circulatory messages to the gut via brain-gut axis reflecting changes in corticotrophin releasing hormone, mast cells activity, neurotransmission at the autonomic nerves system and intestinal barrier function all affecting the pathogenesis of animal colitis and human IBD. Stress triggers the hypothalamus-pituitary axis and the activation of the autonomic nervous system, an increase in cortisol levels and proinflammatory cytokines such as tumor necrosis factor-alpha, interleukin-8, interleukin-1beta and interleukin-6.
The acute or chronic stress enhances the intestinal permeability weakening of the tight junctions and increasing bacterial translocation into the intestinal wall. An increased microbial load in the colonic tissue, excessive cytokine release and a partially blunted immune reactivity in response to stress result in its negative impact on IBD.
已知不同来源的应激会改变所谓的“脑-肠轴”,并导致一系列胃肠道疾病,包括炎症性肠病(IBD)、肠易激综合征(IBS)和其他功能性胃肠道疾病。应激情况和各种应激源,包括心理社会事件、热、体温过低和过高,可能通过未知机制使IBD的病情恶化。本文的目的是概述实验和临床证据,即应激激活脑-肠轴,导致黏膜肥大细胞活化,并增加促炎细胞因子以及其他内分泌和体液介质的产生。
回顾了与应激对下消化道疾病影响相关的研究和在线内容,并阐述了最重要的机制。
大脑通过脑-肠轴将神经、内分泌和循环信息传递给肠道,反映促肾上腺皮质激素释放激素、肥大细胞活性、自主神经系统的神经传递以及肠屏障功能的变化,所有这些都影响动物结肠炎和人类IBD的发病机制。应激会触发下丘脑-垂体轴和自主神经系统的激活,导致皮质醇水平以及肿瘤坏死因子-α、白细胞介素-8、白细胞介素-1β和白细胞介素-6等促炎细胞因子增加。
急性或慢性应激会增强肠道通透性,削弱紧密连接,并增加细菌易位进入肠壁。结肠组织中微生物负荷增加、细胞因子过度释放以及对应激的免疫反应部分减弱,都会对IBD产生负面影响。