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首页> 外文期刊>Neurogastroenterology and motility >Enteric glial cells are associated with stress-induced colonic hyper-contraction in maternally separated rats
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Enteric glial cells are associated with stress-induced colonic hyper-contraction in maternally separated rats

机译:肠源性胶质细胞与母体分离大鼠的应激诱导的结肠过度收缩有关

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Background Enteric glial cells (EGCs) play important roles in enteric integrity and regulation of gastrointestinal function. However, whether EGCs undergo pathophysiological changes in stress-associated gastrointestinal disorders is unknown. We investigated structural and functional alterations in colonic EGCs and their roles in colonic contraction in an irritable bowel syndrome (IBS) model. Methods As a chronic stress, male Wistar rats underwent 3-h maternal separation during postnatal days 2-14. As an acute stress, we used water-immersion stress (4 h) in adulthood (at 8 weeks). We quantitatively and morphologically evaluated enteric neurons and EGCs using whole-mount longitudinal muscle-myenteric plexus preparations. Colonic contraction was analyzed with electrical field stimulation (EFS). Key Results Glial fibrillary acidic protein (GFAP) expression and the number of total, cholinergic, and nitrergic neurons were unchanged in maternally separated rats with acute stress(combined stress: an IBS model) compared with controls. However, the density of GFAP-positive EGC processes that apparently overlapped with the neurons and the extent of bulbous swelling of terminals increased according to the stress intensity: control, acute stress, maternal separation, and combined stress. EFS-induced colonic contractions were significantly greater in the combined stress rats than in controls. Higher dose of fluorocitrate, a selective inhibitor of EGC metabolism, was required to inhibit both EFS-induced contraction and EGCs activation in the combined stress rats than in controls. Conclusions & Inferences Colonic EGCs exhibited structural alterations according to the stress intensity. EGCs were associated with stress-induced colonic hyper-contraction in the combined stress rats, which may underlie the pathogenesis of IBS.
机译:背景肠神经胶质细胞(EGC)在肠完整性和胃肠功能调节中起重要作用。但是,EGC是否在应激相关的胃肠道疾病中发生病理生理变化尚不清楚。我们调查了肠易激综合征的结构和功能改变及其在肠易激综合征(IBS)模型中结肠收缩中的作用。方法作为慢性应激,雄性Wistar大鼠在出生后2-14天进行了3小时的母体分离。作为急性应激,我们在成年期(第8周)使用了浸水应激(4小时)。我们使用整体式纵向肌肉-肠系膜神经丛制剂对肠道神经元和EGC进行定量和形态学评估。用电场刺激(EFS)分析结肠收缩。关键结果母体分离的急性应激大鼠(合并应激:IBS模型)与对照组相比,胶质纤维酸性蛋白(GFAP)的表达以及总,胆碱能和亚硝酸能神经元的数量没有变化。但是,GFAP阳性EGC过程的密度明显与神经元重叠,并且末端的球状肿胀程度根据压力强度而增加:控制,急性压力,母体分离和综合压力。 EFS诱导的结肠收缩在联合应激大鼠中明显大于对照组。与对照组相比,在合并的应激大鼠中,需要更高剂量的氟柠檬酸作为EGC代谢的选择性抑制剂,才能抑制EFS诱导的收缩和EGC激活。结论与推论结肠EGC根据应力强度表现出结构变化。在合并的应激大鼠中,EGC与应激诱导的结肠过度收缩有关,这可能是IBS发病的基础。

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