首页> 外文期刊>Molecular Nutrition and Food Research >A nondigestible saccharide, fructooligosaccharide,increases the promotive effect of a flavonoid,-glucosyl-isoquercitrin, on glucagon-likepeptide 1 (GLP-1) secretion in rat intestineand enteroendocrine cells
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A nondigestible saccharide, fructooligosaccharide,increases the promotive effect of a flavonoid,-glucosyl-isoquercitrin, on glucagon-likepeptide 1 (GLP-1) secretion in rat intestineand enteroendocrine cells

机译:一种不可消化的糖,低聚果糖,增加了类黄酮-葡萄糖基-异槲皮苷对大鼠肠和肠内分泌细胞胰高血糖素样肽1(GLP-1)分泌的促进作用。

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摘要

This study conducted in vivo and in situ experiments with rats to investigate the glucagon-likepeptide-1 (GLP-1) secretion in response to oral or ileal administration of -glucosyl-isoquercitrin(20–40 mmol in 2 mL; Q3G), fructooligosaccharides (200 mmol in 2 mL; FOS) and Q3G +FOS. Direct effects on GLP-1-producingL-cells were also examined by an in vitro study using amurine enteroendocrine cell line, GLUTag. To evaluate the plasma GLP-1 level, blood samplesfrom jugular cannula for in vivo and portalcannula for in situ experiments were obtained beforeand after administration of Q3G, FOS, or Q3G + FOS. We found tendencies for increases buttransient stimulation of GLP-1 secretion by Q3G in in vivo and in situ experiments. AlthoughFOS alone did not have any effects, Q3G + FOS enhanced and prolonged high plasma GLP-1level in both experiments. In addition, application of Q3G on GLUTag cells stimulated GLP-1secretion while FOS enhanced the effect of Q3G. Our results suggest that Q3G + FOS pos-sess the potential for the management or prevention of Type 2 diabetes mellitus (T2DM) byenhancing and prolonging the GLP-1 secretion via direct stimulation of GLP-1 producingL-cell.
机译:这项研究与大鼠进行了体内和原位实验,研究了口服或回肠给予-葡萄糖基-异槲皮苷(2mL中20–40 mmol; Q3G),低聚果糖的胰高血糖素样肽1(GLP-1)的分泌。 (在2 mL中为200 mmol; FOS)和Q3G + FOS。还通过使用鼠科肠内分泌细胞系GLUTag进行的体外研究,检查了对产生GLP-1的L细胞的直接作用。为了评估血浆GLP-1水平,在施用Q3G,FOS或Q3G + FOS之前和之后,分别从体内颈静脉插管的血样和原位实验的门静脉插管的血样中获取。我们在体内和原位实验中发现了Q3G增加但短暂刺激GLP-1分泌的趋势。尽管单独的FOS并没有任何作用,但在两个实验中Q3G + FOS都可以增强并延长血浆GLP-1的高水平。此外,在GLUTag细胞上施用Q3G刺激了GLP-1分泌,而FOS增强了Q3G的作用。我们的研究结果表明,Q3G + FOS通过直接刺激产生GLP-1的L细胞来增强和延长GLP-1的分泌,从而具有管理或预防2型糖尿病(T2DM)的潜力。

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