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压力与胃肠道

Stress and the gastrointestinal tract.

作者信息

Bhatia Vikram, Tandon Rakesh K

机构信息

Department of Gastroenterology and Human Nutrition, All India Institute of Medical Sciences, New Delhi, India.

出版信息

J Gastroenterol Hepatol. 2005 Mar;20(3):332-9. doi: 10.1111/j.1440-1746.2004.03508.x.

Abstract

Stress, defined as an acute threat to homeostasis, evokes an adaptive or allostatic response and can have both a short- and long-term influence on the function of the gastrointestinal tract. The enteric nervous system is connected bidirectionally to the brain by parasympathetic and sympathetic pathways forming the brain-gut axis. The neural network of the brain, which generates the stress response, is called the central stress circuitry and includes the paraventricular nucleus of the hypothalamus, amygdala and periaqueductal gray. It receives input from the somatic and visceral afferent pathways and also from the visceral motor cortex including the medial prefrontal, anterior cingulate and insular cortex. The output of this central stress circuit is called the emotional motor system and includes automatic efferents, the hypothalamus-pituitary-adrenal axis and pain modulatory systems. Severe or long-term stress can induce long-term alteration in the stress response (plasticity). Corticotropin releasing factor (CRF) is a key mediator of the central stress response. Two CRF receptor subtypes, R1 and R2, have been described. They mediate increased colonic motor activity and slowed gastric emptying, respectively, in response to stress. Specific CRF receptor antagonists injected into the 0 block these visceral manifestations of stress. Circulating glucocorticoids exert an inhibitory effect on the stress response by receptors located in the medial prefrontal cortex and hippocampus. Many other neurotransmitters and neuroimmunomodulators are being evaluated. Stress increases the intestinal permeability to large antigenic molecules. It can lead to mast cell activation, degranulation and colonic mucin depletion. A reversal of small bowel water and electrolyte absorption occurs in response to stress and is mediated cholinergically. Stress also leads to increased susceptibility to colonic inflammation, which can be adaptively transferred among rats by sensitized CD4(+) lymphocytes. The association between stress and various gastrointestinal diseases, including functional bowel disorders, inflammatory bowel disease, peptic ulcer disease and gastroesophageal reflux disease, is being actively investigated. Attention to the close relation between the brain and gut has opened many therapeutic avenues for the future.

摘要

应激被定义为对体内平衡的急性威胁,它会引发适应性或稳态应变反应,并可对胃肠道功能产生短期和长期影响。肠神经系统通过形成脑-肠轴的副交感神经和交感神经通路与大脑双向连接。产生应激反应的大脑神经网络被称为中枢应激回路,包括下丘脑室旁核、杏仁核和导水管周围灰质。它接收来自躯体和内脏传入通路的输入,也接收来自包括内侧前额叶、前扣带回和岛叶皮质在内的内脏运动皮质的输入。这个中枢应激回路的输出被称为情绪运动系统,包括自主传出神经、下丘脑-垂体-肾上腺轴和疼痛调节系统。严重或长期应激可导致应激反应的长期改变(可塑性)。促肾上腺皮质激素释放因子(CRF)是中枢应激反应的关键介质。已描述了两种CRF受体亚型,R1和R2。它们分别介导应激反应时结肠运动活性增加和胃排空减慢。向脑内注射特异性CRF受体拮抗剂可阻断这些应激的内脏表现。循环糖皮质激素通过位于内侧前额叶皮质和海马体的受体对应激反应发挥抑制作用。许多其他神经递质和神经免疫调节剂正在进行评估。应激会增加肠道对大抗原分子的通透性。它可导致肥大细胞活化、脱颗粒和结肠粘蛋白耗竭。应激会引起小肠水和电解质吸收的逆转,这是由胆碱能介导的。应激还会导致结肠炎症易感性增加,致敏的CD4(+)淋巴细胞可在大鼠之间适应性地传递这种易感性。应激与包括功能性肠病、炎症性肠病、消化性溃疡病和胃食管反流病在内的各种胃肠道疾病之间的关联正在积极研究中。对脑与肠密切关系的关注为未来开辟了许多治疗途径。

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