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Study of glucose concentrated solution consumption in rats and simulation of glucose distribution along the intestine

机译:大鼠葡萄糖浓缩液消耗的研究及肠道内葡萄糖分布的模拟

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Free ingestion of glucose solution (200 or 400 g/l) by Wistar rats, previously starved for 18-20 Hrs, was investigated in two groups of the animals: with intact small intestine (group 1, n = 9), and a shortened small intestine following the Thiry-Wella isolation of its one third proximal part (group 2, n = 9). In the rats of the group 2, the isolated intestinal loops were perfused in chronic experiments with soulutions of different glucose concentrations to estimate a permeability of the pre-epithelial ("unstirred") layer and "true" kinetic constants of glucose active transport. The rate of glusouse ingestion was found to be 1.3-fold as high in the of rats fgroup 1 than in the rats of group 2 (p < 0.01). According to results of mathematical modeling, the rate of glucose ingestion by rats corresponds to glucose concentration in the initial solutions and to the absorbing capacity of the small intestine due to the substrate regulation of gastric emptying. The model predicts that, during free ingestion by rats of 400 g/l (2200 mM) glucose solution, the substrate concentration in the intestinal lumen under steady state conditions hardly exceeds 75 mM. This fact contradicts a recently proposed hypothesis about a facilitated transport mediated by GLUT2 as the main mechanism of glucose absorption in the small intestine under normal conditions.
机译:在两组动物中研究了先前饥饿18-20小时的Wistar大鼠自由摄入的葡萄糖溶液(200或400 g / l):完整的小肠动物(第1组,n = 9)和缩短的动物Thiry-Wella分离其第三近端部分后的小肠(第2组,n = 9)。在第2组的大鼠中,在慢性实验中用不同葡萄糖浓度的果汁灌肠分离的肠loop,以估计上皮前(“未搅拌”)层的渗透性和葡萄糖活性转运的“真实”动力学常数。在第1组大鼠中,摄取小胶质的速率是第2组大鼠的1.3倍(p <0.01)。根据数学模型的结果,大鼠的葡萄糖摄取速率与初始溶液中的葡萄糖浓度相对应,并且与由于胃排空的底物调节而导致的小肠的吸收能力相对应。该模型预测,在大鼠自由摄取400 g / l(2200 mM)葡萄糖溶液的过程中,稳态条件下肠腔中的底物浓度几乎不会超过75 mM。这一事实与最近提出的关于由GLUT2介导的促进运输作为正常条件下小肠中葡萄糖吸收的主要机制的假设相矛盾。

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