首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >T1R3 and gustducin in gut sense sugars to regulate expression of Na~+ -glucose cotransporter 1
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T1R3 and gustducin in gut sense sugars to regulate expression of Na~+ -glucose cotransporter 1

机译:肠糖中的T1R3和gustgustin调节Na〜+-葡萄糖共转运蛋白1的表达

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摘要

Dietary sugars are transported from the intestinal lumen into absorptive enterocytes by the sodium-dependent glucose transporter isoform 1 (SGLT1). Regulation of this protein is important for the provision of glucose to the body and avoidance of intestinal malabsorption. Although expression of SGLT1 is regulated by luminal monosaccharides, the luminal glucose sensor mediating this process was unknown. Here, we show that the sweet taste receptor subunitT1R3 and the taste G protein gustducin, expressed in enteroendocrine cells, underlie intestinal sugar sensing and regulation of SGLT1 mRNA and protein. Dietary sugar and artificial sweeteners increased SGLT1 mRNA and protein expression, and glucose absorptive capacity in wild-type mice, but not in knockout mice lacking T1R3 or α-gustducin. Artificial sweeteners, acting on sweet taste receptors expressed on enteroendocrine GLUTag cells, stimulated secretion of gut hormones implicated in SGLT1 up-regulation. Gut-expressed taste signaling elements involved in regulating SGLT1 expression could provide novel therapeutic targets for modulating the gut's capacity to absorb sugars, with implications for the prevention and/or treatment of malabsorption syndromes and diet-related disorders including diabetes and obesity.
机译:饮食糖通过钠依赖性葡萄糖转运蛋白同工型1(SGLT1)从肠腔运输到吸收性肠细胞中。这种蛋白质的调节对于向人体提供葡萄糖和避免肠道吸收不良很重要。尽管SGLT1的表达受腔单糖调节,但介导该过程的腔葡萄糖传感器尚不清楚。在这里,我们显示在肠内分泌细胞中表达的甜味受体亚基T1R3和味觉G蛋白gustducin是肠道糖感测和SGLT1 mRNA和蛋白调控的基础。在野生型小鼠中,膳食糖和人造甜味剂可增加SGLT1 mRNA和蛋白表达以及葡萄糖吸收能力,而缺乏T1R3或α-gustducin的基因敲除小鼠则不能。人造甜味剂可作用于肠内分泌GLUTag细胞上表达的甜味受体,刺激与SGLT1上调有关的肠道激素的分泌。肠道表达的味觉信号元件参与调节SGLT1表达,可以为调节肠道吸收糖分的能力提供新的治疗靶标,对预防和/或治疗吸收不良综合征和与饮食有关的疾病(包括糖尿病和肥胖症)具有意义。

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