Spitz J C, Ghandi S, Taveras M, Aoys E, Alverdy J C
Department of Surgery, University of Illinois, Chicago, USA.
Crit Care Med. 1996 Apr;24(4):635-41. doi: 10.1097/00003246-199604000-00015.
a) To determine the significance of stress-induced alterations in intestinal permeability by measuring the transmucosal flux of formyl-methionyl-leucyl-phenylalanine (f-MLP), a ubiquitous neutrophilic chemoattractant present in the human and rodent colon; and b) to determine whether stress and/or diet influence(s) bacterial adherence-induced changes in epithelial permeability by affecting the production of secretory immunoglobulin A (IgA), the main immune mechanism preventing bacterial adherence.
Prospective, randomized, controlled study.
University animal research laboratory.
Female Fischer rats.
Rats were randomly assigned to four groups of seven animals each. Groups of animals were assigned to receive saline or dexamethasone (0.8 mg/kg ip) and were either starved (5% dextrose in water ad libitum) or fed (water and rat chow) for 48 hrs.
Mucosal barrier function was evaluated by measuring secretory IgA, bacterial adherence to the intestinal mucosa, and transepithelial electrical resistance, a measure of tight junction permeability. The f-MLP permeation across the mucosa was also determined in segments with significant permeability changes. Results indicate that starvation in dexamethasone-treated rats significantly impairs secretory IgA, promotes bacterial adherence to the mucosa, and results in increased intestinal permeability to f-MLP. These effects are significantly attenuated by the feeding of rat chow.
Alterations in intestinal barrier function are characterized by depressed IgA, bacterial adherence to the intestinal mucosa, and permeation of clinically relevant proinflammatory luminal macromolecules (f-MLP). Enteral stimulation with foodstuffs is a necessary protective measure to prevent altered epithelial barrier function during glucocorticoid stress.
a)通过测量甲酰甲硫氨酰亮氨酰苯丙氨酸(f-MLP)的跨粘膜通量来确定应激诱导的肠道通透性改变的意义,f-MLP是人和啮齿动物结肠中普遍存在的嗜中性粒细胞趋化因子;b)确定应激和/或饮食是否通过影响分泌型免疫球蛋白A(IgA)的产生来影响细菌粘附诱导的上皮通透性变化,IgA是防止细菌粘附的主要免疫机制。
前瞻性、随机、对照研究。
大学动物研究实验室。
雌性Fischer大鼠。
将大鼠随机分为四组,每组七只动物。给动物分组,使其接受生理盐水或地塞米松(0.8mg/kg腹腔注射),并使其禁食(随意饮用5%葡萄糖水)或喂食(水和大鼠饲料)48小时。
通过测量分泌型IgA、细菌对肠粘膜的粘附以及跨上皮电阻(一种紧密连接通透性的测量指标)来评估粘膜屏障功能。还在通透性有显著变化的节段中测定f-MLP跨粘膜的渗透情况。结果表明,地塞米松处理的大鼠禁食会显著损害分泌型IgA,促进细菌对粘膜的粘附,并导致肠道对f-MLP的通透性增加。喂食大鼠饲料可显著减轻这些影响。
肠道屏障功能的改变表现为IgA降低、细菌对肠粘膜的粘附以及临床相关促炎腔内大分子(f-MLP)的渗透。食物的肠内刺激是预防糖皮质激素应激期间上皮屏障功能改变的必要保护措施。