Suppr超能文献

二甲双胍可刺激人肠道黏膜分泌 PYY。

Metformin Triggers PYY Secretion in Human Gut Mucosa.

机构信息

College of Medicine and Public Health, Flinders University, Bedford Park, South Australia, Australia.

Department of Surgery, Flinders Medical Centre, Bedford Park, South Australia, Australia.

出版信息

J Clin Endocrinol Metab. 2019 Jul 1;104(7):2668-2674. doi: 10.1210/jc.2018-02460.

Abstract

CONTEXT

The antidiabetic drug metformin causes weight loss, but the underlying mechanisms are unclear. Recent clinical studies show that metformin increases plasma levels of the anorectic gut hormone, peptide YY (PYY), but whether this is through a direct effect on the gut is unknown.

OBJECTIVE

We hypothesized that exposure of human gut mucosal tissue to metformin would acutely trigger PYY secretion.

DESIGN, SETTING, PARTICIPANTS, AND INTERVENTIONS: Mucosal tissue was prepared from 46 human colonic and 9 ileal samples obtained after surgical resection and ex vivo secretion assays were performed. Tissue was exposed to metformin, as well as a series of other compounds as part of our mechanistic studies, in static incubations. Supernatant was sampled after 15 minutes.

MAIN OUTCOME MEASURES

PYY levels in supernatant, measured using ELISA.

RESULTS

Metformin increased PYY secretion from both ileal (P < 0.05) and colonic (P < 0.001) epithelia. Both basal and metformin-induced PYY secretion were unchanged across body mass index or in tissues obtained from individuals with type 2 diabetes. Metformin-dependent PYY secretion was blocked by inhibitors of the plasma membrane monoamine transporter (PMAT) and the serotonin reuptake transporter (SERT), as well as by an inhibitor of AMP kinase (AMPK).

CONCLUSIONS

This is a report of a direct action of metformin on the gut epithelium to trigger PYY secretion in humans, occurring via cell internalization through PMAT and SERT and intracellular activation of AMPK. Our results provide further support that the role of metformin in the treatment of metabolic syndrome has a gut-based component.

摘要

背景

抗糖尿病药物二甲双胍可导致体重减轻,但潜在机制尚不清楚。最近的临床研究表明,二甲双胍可增加厌食性肠道激素肽 YY(PYY)的血浆水平,但这是否是通过对肠道的直接作用尚不清楚。

目的

我们假设暴露于人体肠道黏膜组织中的二甲双胍会急性触发 PYY 分泌。

设计、设置、参与者和干预措施:从 46 个人结肠和 9 个人回肠样本中制备黏膜组织,这些样本是在手术切除后获得的,并进行了离体分泌测定。组织在静态孵育中暴露于二甲双胍以及一系列其他化合物,作为我们的机制研究的一部分。孵育 15 分钟后取样上清液。

主要观察指标

使用 ELISA 测量上清液中的 PYY 水平。

结果

二甲双胍增加了回肠(P < 0.05)和结肠(P < 0.001)上皮的 PYY 分泌。无论身体质量指数如何,或从 2 型糖尿病患者获得的组织中,基础和二甲双胍诱导的 PYY 分泌均无变化。PMAT 和 SERT 的抑制剂以及 AMP 激酶(AMPK)抑制剂阻断了二甲双胍依赖性 PYY 分泌。

结论

这是二甲双胍对人类肠道上皮细胞直接作用以触发 PYY 分泌的报告,通过 PMAT 和 SERT 的细胞内化和细胞内 AMPK 的激活来发生。我们的结果进一步支持了二甲双胍在代谢综合征治疗中的作用具有肠道成分。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验