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首页> 外文期刊>Biochimica et biophysica acta: international journal of biochemistry and biophysics >Regulation of rat intestinal GLUT2 mRNA abundance by luminal and systemic factors.
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Regulation of rat intestinal GLUT2 mRNA abundance by luminal and systemic factors.

机译:管腔和全身因素对大鼠肠道GLUT2 mRNA丰度的调节。

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Fructose in the lumen of the small intestine is transported across the brush border membrane by GLUT5, then across the basolateral membrane by GLUT2, which also transports glucose. Diets containing high fructose (HF) specifically enhance intestinal GLUT5 expression in neonatal rats, but there is little information concerning the dietary regulation of GLUT2 expression during early development. In this study, we perfused for 1-4 h 100 mM fructose, glucose (HG), alpha-methylglucose, or mannitol solutions into the jejunum of anaesthetized 20-day-old rat pups. GLUT2 mRNA abundance increased only in HF- and HG-perfused intestines, an effect inhibited by actinomycin D but not by cycloheximide. Bypassed (Thiry-Vella) intestinal loops were constructed, then pups were fed either HF or low-carbohydrate diets for 5 days. GLUT2 mRNA abundance increased significantly in both bypassed and anastomosed intestines of Thiry-Vella pups fed HF. In contrast, GLUT5 mRNA abundance increased only in the anastomosed segment. Insham-operated pups, GLUT2 and GLUT5 mRNA abundance increased in both intestinal regions that corresponded to the bypassed and anastomosed regions of Thiry-Vella pups. SGLT1 mRNA abundance was independent of diet and intestinal region in both Thiry-Vella and sham-operated pups. Unlike GLUT5 expression, which is regulated at the level of transcription only by luminal fructose, GLUT2 mRNA expression is transcriptionally regulated by luminal fructose and glucose as well as by systemic factors released during their absorption.
机译:小肠腔中的果糖通过GLUT5转运穿过刷状缘膜,然后通过GLUT2转运穿过基底外侧膜,后者也转运葡萄糖。含高果糖(HF)的饮食可特异性增强新生大鼠肠道GLUT5的表达,但有关早期发育期间GLUT2表达的饮食调节的信息很少。在这项研究中,我们将1-4小时的100 mM果糖,葡萄糖(HG),α-甲基葡萄糖或甘露醇溶液灌注到麻醉的20天大的幼仔空肠中。 GLUT2 mRNA的丰度仅在灌注HF和HG的肠道中增加,这一作用被放线菌素D抑制,但未被环己酰亚胺抑制。构建绕过的(Thiry-Vella)肠环,然后给幼犬饲喂HF或低碳水化合物饮食5天。饲喂HF的Thiry-Vella幼犬的肠旁路和吻合肠中的GLUT2 mRNA丰度均显着增加。相反,GLUT5 mRNA丰度仅在吻合段增加。假手术的幼犬,GLUT2和GLUT5 mRNA的丰度在两个肠道区域均增加,这与Thiry-Vella幼犬的旁路和吻合区域相对应。在Thiry-Vella和假手术的幼崽中,SGLT1 mRNA的丰度与饮食和肠道区域无关。与GLUT5表达仅在果糖中调节转录水平不同,GLUT2 mRNA的表达受果糖和葡萄糖以及吸收过程中释放的全身性因子的转录调节。

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