al-Majali A, Asem E, Lamar C, Robinson J P, Freeman M J, Saeed M
Department of Veterinary Pathobiology, School of Veterinary Medicine, Purdue University, West Lafayette, IN 47907, USA.
Vet Res. 1998 Nov-Dec;29(6):527-36.
Effect of insulin on the response of suckling mice to the enterotoxigenic Escherichia coli heat-stable enterotoxin (STa) was studied. Four groups (8-10 in each group) of 2-day-old Swiss Webster suckling mice were used. For this study, 5, 10, 25 and 50 micrograms of insulin was given orally to half the mice in each group for 7 days. The rest of the mice in each group were given normal saline as intra-litter controls. After 7 days, a suckling mouse assay in which 1 microgram of STa was given to all mice in insulin-treated and control groups was performed. Enterocyte suspensions were prepared from mice in all groups. Intestinal tissue samples were taken for electron microscopy. Interaction of STa with its putative receptor on the enterocytes was evaluated using indirect immunofluorescence and flow cytometry. The suckling mouse assay revealed a significant increase in the gut weight to body weight ratio in all mice in the insulin-treated groups compared to control mice (P < 0.05). Flow cytometry and indirect immunofluorescence analyses suggested that insulin had an up-regulatory effect on the STa-receptor level. Similarly, insulin was found to increase intestinal brush border membrane differentiation as indicated by the increase in the inward movement of milk particles through the intestinal mucosa. Insulin seems to modify the structure-function of the brush border membrane including the response of suckling mice to STa. This study may provide further insights into the mechanism of STa/receptor interaction, which is a major cause of diarrhea in newborn animals and human infants.
研究了胰岛素对乳鼠对产肠毒素大肠杆菌热稳定肠毒素(STa)反应的影响。使用了四组(每组8 - 10只)2日龄的瑞士韦伯斯特乳鼠。在本研究中,每组半数乳鼠口服5、10、25和50微克胰岛素,持续7天。每组其余乳鼠给予生理盐水作为同窝对照。7天后,对胰岛素处理组和对照组的所有小鼠进行乳鼠试验,给它们注射1微克STa。从所有组的小鼠制备肠上皮细胞悬液。取肠道组织样本进行电子显微镜检查。使用间接免疫荧光和流式细胞术评估STa与其在肠上皮细胞上的假定受体的相互作用。乳鼠试验显示,与对照小鼠相比,胰岛素处理组所有小鼠的肠重与体重比显著增加(P < 0.05)。流式细胞术和间接免疫荧光分析表明,胰岛素对STa受体水平有上调作用。同样,如牛奶颗粒通过肠黏膜向内移动增加所示,胰岛素可增加肠道刷状缘膜的分化。胰岛素似乎改变了刷状缘膜的结构功能,包括乳鼠对STa的反应。本研究可能为STa/受体相互作用机制提供进一步的见解,STa/受体相互作用是新生动物和人类婴儿腹泻的主要原因。