To Determine the Effect of Endogenous GLP-1 Secretion on Islet Function in People With and Without Type 2 Diabetes
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
- Adrian Vella
- 入组人数
- 23
- 试验地点
- 1
- 主要终点
- Change in Fasting Glucagon in the Presence or Absence of Exendin-9,39
研究概览
简要总结
GLP-1 is a hormone made by the body that promotes the production of insulin in response to GLP-1 is produced within the islets expressing prohormone convertase 1/3eating. However, there is increasing evidence that this hormone might help support the body's ability to produce insulin when diabetes develops. The purpose of this study is to determine the effect of endogenous GLP-1 secretion on insulin secretion in people with and without type 2 diabetes.
详细描述
Accumulating evidence suggests that in rodents and humans GLP-1 is synthesized within islets and may act locally in a paracrine fashion. Indeed, mice with genetic loss of intra-islet GLP-1 exhibit decreased insulin secretion and impaired response to metabolic stressors. 'Pancreatic' GLP-1 may contribute to the effects of DPP-4 inhibitors in rodents and humans. Antagonism of GLP1R with exendin-9,39 during fasting impairs the islet cell response to an I.V. glucose challenge. Islet GLP-1 content is increased in T2DM and in islets from non-diabetic humans exposed to hyperglycemia and Free Fatty Acids. These observations imply that paracrine GLP-1 secretion supports islet function in the presence of glucolipotoxicity. In this experiment we will examine the role of endogenous GLP-1 secretion in people with and without T2DM and during β-cell stress induced by FFA elevation.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Basic Science
- 盲法
- None
入排标准
- 年龄范围
- 25 Years 至 65 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •non-diabetic subjects:
- •Weight-stable, non-diabetic subjects
排除标准
- •non-diabetic subjects:
- •Age < 25 or > 65 years (to avoid studying subjects who could have latent type 1 diabetes, or the effects of age extremes in subjects with normal or impaired fasting glucose).
- •HbA1c ≥ 6.5%
- •Use of glucose-lowering agents.
- •For female subjects: positive pregnancy test at the time of enrollment or study
- •History of prior upper abdominal surgery such as adjustable gastric banding, pyloroplasty and vagotomy.
- •Active systemic illness or malignancy.
- •Symptomatic macrovascular or microvascular disease.
- •Inclusion criteria - diabetic subjects:
- •Weight-stable, diabetic subjects treated with diet and lifestyle alone or with metformin monotherapy
- •Exclusion Criteria - diabetic subjects:
- •Age < 25 or > 65 years (to avoid studying subjects who could have latent type 1 diabetes, or the effects of age extremes in subjects with normal or impaired fasting glucose).
- •Use of any glucose-lowering agent other than metformin.
- •2 or more fasting glucose values > 250mg/dl on medication or after medication withdrawal.
- •Unwillingness or inability to withdraw medication for three weeks prior to, and for the duration of the study.
- •For female subjects: positive pregnancy test at the time of enrollment or study
- •History of prior upper abdominal surgery such as adjustable gastric banding, pyloroplasty and vagotomy.
- •Active systemic illness or malignancy.
- •Symptomatic macrovascular or microvascular disease.
研究组 & 干预措施
Exendin-9,39
Exendin-9,39 infusion
干预措施: Exendin-9,39 (Biological)
Saline
Saline infusion
干预措施: Saline (Biological)
Saline + Intralipid/Heparin
Induction of acute insulin resistance during Saline infusion
干预措施: Saline + Intralipid/Heparin (Biological)
Exendin-9,39 + Intralipid/Heparin
Induction of acute insulin resistance during Exendin-9,39 infusion
干预措施: Exendin-9,39 + Intralipid/Heparin (Biological)
结局指标
主要结局
Change in Fasting Glucagon in the Presence or Absence of Exendin-9,39
时间窗: Average concentration over the -30 to 0 minutes of study
Concentrations of glucagon Measured by immunoassay over the -30 to 0 minutes of study. On one study day subjects received saline, on the other exendin-9,39. The infusion commenced at -120 minutes.
次要结局
未报告次要终点