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Interaction of GLP-1 and Ghrelin on Glucose Tolerance in Healthy Humans

机译:GLP-1和Ghrelin对健康人葡萄糖耐量的相互作用

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摘要

Emerging evidence supports the importance of ghrelin to defend against starvation-induced hypoglycemia. This effect may be mediated by inhibition of glucose-stimulated insulin secretion as well as reduced insulin sensitivity. However, administration of ghrelin during meal consumption also stimulates the release of glucagon-like peptide 1 (GLP-1), an incretin important in nutrient disposition. The objective of this study was to evaluate the interaction between ghrelin and GLP-1 on parameters of glucose tolerance following a mixed-nutrient meal. Fifteen healthy men and women completed the study. Each consumed a standard meal on four separate occasions with a superimposed infusion of 1) saline, 2) ghrelin, 3) the GLP-1 receptor antagonist exendin(9-39) (Ex9), or 4) combined ghrelin and Ex9. Similar to previous studies, infusion of ghrelin caused glucose intolerance, whereas Ex9 had a minimal effect. However, combined ghrelin and Ex9 resulted in greater postprandial glycemia than either alone, and this effect was associated with impaired β-cell function and decreased glucose clearance. These findings suggest that in the fed state, stimulation of GLP-1 mitigates some of the effect of ghrelin on glucose tolerance. This novel interaction between gastrointestinal hormones suggests a system that balances insulin secretion and glucose disposal in the fed and fasting states.
机译:越来越多的证据支持生长素释放肽对抵抗饥饿引起的低血糖的重要性。该作用可以通过抑制葡萄糖刺激的胰岛素分泌以及降低胰岛素敏感性来介导。但是,在进餐期间服用生长素释放肽还可以刺激胰高血糖素样肽1(GLP-1)的释放,胰高血糖素样肽1在营养素处置中起重要作用。这项研究的目的是评估混合营养餐后生长素释放肽和GLP-1在葡萄糖耐量参数上的相互作用。十五名健康的男人和女人完成了这项研究。每个人在四个单独的场合食用标准餐,并叠加输注1)盐水,2)ghrelin,3)GLP-1受体拮抗剂exendin(9-39)(Ex9)或4)ghrelin和Ex9的组合。与以前的研究相似,输注生长激素释放肽会引起葡萄糖耐受不良,而Ex9的影响最小。但是,ghrelin和Ex9的联合使用比单独使用会导致更高的餐后血糖,这种作用与β细胞功能受损和葡萄糖清除率降低有关。这些发现表明,在进食状态下,GLP-1的刺激减轻了生长素释放肽对葡萄糖耐量的某些影响。胃肠激素之间的这种新颖的相互作用提示了一种在进食和空腹状态下平衡胰岛素分泌和葡萄糖处置的系统。

著录项

  • 来源
    《Diabetes》 |2018年第10期|1976-1985|共10页
  • 作者单位

    Division of Endocrinology, Department of Pediatrics, Duke University, Durham, NC;

    Institute of Clinical Physiology, National Research Council, Pisa, Italy;

    Duke Molecular Physiology Institute, Duke University, Durham, NC;

    Duke Molecular Physiology Institute, Duke University, Durham, NC,Division of Endocrinology, Diabetes and Metabolism, Department of Medicine, University of Cincinnati, Cincinnati, OH,Division of Endocrinology, Metabolism, and Nutrition, Department of Medicine, Duke University, Durham, NC,Cincinnati VA Medical Center, Cincinnati, OH;

    Duke Molecular Physiology Institute, Duke University, Durham, NC,Division of Endocrinology, Diabetes and Metabolism, Department of Medicine, University of Cincinnati, Cincinnati, OH,Division of Endocrinology, Metabolism, and Nutrition, Department of Medicine, Duke University, Durham, NC;

  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-18 04:08:38

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