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旁路近端肠道对参与血糖控制和体重减轻的肠道激素的影响。

Effect of bypassing the proximal gut on gut hormones involved with glycemic control and weight loss.

机构信息

Imperial Weight Centre, Imperial College London, Charing Cross Hospital, London, United Kingdom.

出版信息

Surg Obes Relat Dis. 2012 Jul-Aug;8(4):371-4. doi: 10.1016/j.soard.2012.01.021. Epub 2012 Mar 3.

Abstract

BACKGROUND

The reported remission of type 2 diabetes in patients undergoing Roux-en-Y gastric bypass has brought the role of the gut in glucose metabolism into focus. Our objective was to explore the differential effects on glucose homeostasis after oral versus gastrostomy glucose loading in patients with Roux-en-Y gastric bypass at an academic health science center.

METHODS

A comparative controlled investigation of oral versus gastrostomy glucose loading in 5 patients who had previously undergone gastric bypass and had a gastrostomy tube placed in the gastric remnant for feeding. A standard glucose load was administered either orally (day 1) or by the gastrostomy tube (day 2). The plasma levels of glucose, insulin, glucagon-like peptide 1 and peptide YY were measured before and after glucose loading.

RESULTS

Exclusion of the proximal small bowel from glucose passage induced greater plasma insulin, glucagon-like peptide 1, and peptide YY responses compared with glucose loading by way of the gastrostomy tube (P <.05).

CONCLUSIONS

Exclusion of glucose passage through the proximal small bowel results in enhanced insulin and gut hormone responses in patients after gastric bypass. The gut plays a central role in glucose metabolism and represents a target for future antidiabetes therapies.

摘要

背景

接受 Roux-en-Y 胃旁路手术的 2 型糖尿病患者的报告缓解,使人们对肠道在葡萄糖代谢中的作用产生了关注。我们的目的是在学术健康科学中心探索 Roux-en-Y 胃旁路手术后患者经口服和胃造口途径给予葡萄糖负荷后对葡萄糖稳态的差异影响。

方法

对 5 例先前接受过胃旁路手术且胃残端放置胃造口管用于喂养的患者进行了口服与胃造口途径葡萄糖负荷的对比对照研究。分别通过口服(第 1 天)或胃造口管(第 2 天)给予标准葡萄糖负荷。在葡萄糖负荷前后测量血糖、胰岛素、胰高血糖素样肽 1 和肽 YY 的血浆水平。

结果

与经胃造口管给予葡萄糖相比,经近端小肠排除葡萄糖会引起更大的血浆胰岛素、胰高血糖素样肽 1 和肽 YY 反应(P <.05)。

结论

胃旁路手术后,近端小肠排除葡萄糖会导致胰岛素和肠道激素反应增强。肠道在葡萄糖代谢中起核心作用,是未来抗糖尿病治疗的靶点。

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