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首页> 外文期刊>Diabetes, obesity & metabolism >Comparative effects of proximal and distal small intestinal administration of metformin on plasma glucose and glucagon‐like peptide‐1, and gastric emptying after oral glucose, in type 2 diabetes
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Comparative effects of proximal and distal small intestinal administration of metformin on plasma glucose and glucagon‐like peptide‐1, and gastric emptying after oral glucose, in type 2 diabetes

机译:二甲双胍对血浆葡萄糖和胰高血糖素样肽-1和口服葡萄糖后胃排空的比较效果,2型糖尿病

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Aims The gastrointestinal tract, particularly the lower gut, may be key to the anti‐diabetic action of metformin. We evaluated whether administration of metformin into the distal, vs the proximal, small intestine would be more effective in lowering plasma glucose by stimulating glucagon‐like pepetide‐1 (GLP‐1) and/or slowing gastric emptying (GE) in type 2 diabetes (T2DM). Materials and methods Ten diet‐controlled T2DM patients were studied on three occasions. A transnasal catheter was positioned with proximal and distal infusion ports located 13 and 190 cm beyond the pylorus, respectively. Participants received infusions of (a) proximal + distal saline (control), (b) proximal metformin (1000 mg) + distal saline or (c) proximal saline + distal metformin (1000 mg) over 5 minutes, followed 60 minutes later by a glucose drink containing 50 g glucose and 150 mg 13 C‐acetate. “Arterialized” venous blood and breath samples were collected over 3 hours for measurements of plasma glucose, GLP‐1, insulin and glucagon, and GE, respectively. Results Compared with control, both proximal and distal metformin reduced plasma glucose and augmented GLP‐1 responses to oral glucose comparably ( P 0.05 each), without affecting plasma insulin or glucagon. GE was slower after proximal metformin than after control ( P 0.05) and tended to be slower after distal metformin, without any difference between proximal and distal metformin. Conclusions In diet‐controlled T2DM patients, glucose‐lowering via a single dose of metformin administered to the upper and lower gut was comparable and was associated with stimulation of GLP‐1 and slowing of GE. These observations suggest that the site of gastrointestinal administration is not critical to the glucose‐lowering capacity of metformin.
机译:旨在胃肠道,特别是下肠道,可能是二甲双胍的抗糖尿病作用的关键。我们评估二甲双胍的给予远端,近端,小肠在通过刺激胰高血糖素样葡萄糖-1(GLP-1)和/或减缓2型糖尿病中的胃排空(GE)中的血浆葡萄糖更有效(T2DM)。材料和方法在三次中研究了10次饮食控制的T2DM患者。跨野导管分别定位在近端和远端输注端口,分别位于幽门螺磁体上的13和190cm。参与者接受了(a)近端+远端盐水(对照),(b)近端二甲双胍(1000mg)+远端盐水或(c)近端盐水+远端盐酸酯(1000mg)超过5分钟,然后通过a含有50g葡萄糖的葡萄糖饮料和150mg 13 c-乙酸盐。在3小时内收集“动脉化”静脉血液和呼吸样品,用于测量血浆葡萄糖,GLP-1,胰岛素和胰高血糖素,GE。结果与对照相比,近端和远端二甲双胍减少了血浆葡萄糖和增强GLP-1对口腔葡萄糖的反应相当(每次P <0.05),不影响血浆胰岛素或胰高血糖素。在近端二甲双胍之后,GE比对照(P <0.05)较慢,并且在远端二甲双胍后倾向于较慢,近端和远端二甲双胍之间的差异。结论在饮食控制的T2DM患者中,通过施用于上肠道和下肠道的单剂量二甲双胍的葡萄糖相当,与GLP-1的刺激相关,GE慢。这些观察结果表明,胃肠道施用的部位对二甲双胍的葡萄糖产能并不重要。

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