Bradesi Sylvie, Schwetz Ines, Ennes Helena S, Lamy Christophe M R, Ohning Gordon, Fanselow Michael, Pothoulakis Charalabos, McRoberts James A, Mayer Emeran A
Department of Medicine, Center for Neurovisceral Sciences and Women's Health, David Geffen School of Medicine at University of California, Greater Los Angeles Veterans Affairs Healthcare System, Los Angeles, California 90073, USA.
Am J Physiol Gastrointest Liver Physiol. 2005 Jul;289(1):G42-53. doi: 10.1152/ajpgi.00500.2004. Epub 2005 Mar 3.
Chronic stress plays an important role in the development and exacerbation of symptoms in functional gastrointestinal disorders. To better understand the mechanisms underlying this relationship, we aimed to characterize changes in visceral and somatic nociception, colonic motility, anxiety-related behavior, and mucosal immune activation in rats exposed to 10 days of chronic psychological stress. Male Wistar rats were submitted daily to either 1-h water avoidance (WA) stress or sham WA for 10 consecutive days. The visceromotor response to colorectal distension, thermal somatic nociception, and behavioral responses to an open field test were measured at baseline and after chronic WA. Fecal pellets were counted after each WA stress or sham WA session as a measure of stress-induced colonic motility. Colonic samples were collected from both groups and evaluated for structural changes and neutrophil infiltration, mast cell number by immunohistochemistry, and cytokine expression by quantitative RT-PCR. Rats exposed to chronic WA (but not sham stress) developed persistent visceral hyperalgesia, whereas only transient changes in somatic nociception were observed. Chronically stressed rats also exhibited anxiety-like behaviors, enhanced fecal pellet excretion, and small but significant increases in the mast cell numbers and the expression of IL-1beta and IFN-gamma. Visceral hyperalgesia following chronic stress persisted for at least a month. Chronic psychological stress in rats results in a robust and long-lasting alteration of visceral, but not somatic nociception. Visceral hyperalgesia is associated with other behavioral manifestations of stress sensitization but was only associated with minor colonic immune activation arguing against a primary role of mucosal immune activation in the maintenance of this phenomenon.
慢性应激在功能性胃肠疾病症状的发生和加重过程中起着重要作用。为了更好地理解这种关系背后的机制,我们旨在描述暴露于10天慢性心理应激的大鼠在内脏和躯体伤害感受、结肠动力、焦虑相关行为以及黏膜免疫激活方面的变化。雄性Wistar大鼠连续10天每天接受1小时的水回避(WA)应激或假WA处理。在基线和慢性WA处理后,测量对结直肠扩张的内脏运动反应、热躯体伤害感受以及对旷场试验的行为反应。在每次WA应激或假WA处理后计数粪便颗粒,作为应激诱导的结肠动力的指标。从两组收集结肠样本,评估结构变化和中性粒细胞浸润、通过免疫组织化学评估肥大细胞数量以及通过定量RT-PCR评估细胞因子表达。暴露于慢性WA(而非假应激)的大鼠出现持续性内脏痛觉过敏,而仅观察到躯体伤害感受的短暂变化。长期应激的大鼠还表现出焦虑样行为、粪便颗粒排泄增加,并且肥大细胞数量以及IL-1β和IFN-γ的表达有小但显著的增加。慢性应激后的内脏痛觉过敏持续至少一个月。大鼠的慢性心理应激导致内脏而非躯体伤害感受的强烈且持久的改变。内脏痛觉过敏与应激敏化的其他行为表现相关,但仅与轻微的结肠免疫激活相关,这表明黏膜免疫激活在维持这种现象中不发挥主要作用。