Overview
This project will describe the mechanisms of action and the relative contributions of GIP to changes in gastrointestinal blood flow induced by oral glucose and endogenous GIP with the use of a receptor antagonists GIP(3-30)NH2 in patients with type 2 diabetes.
Description
Each participant will attend four independent randomised experimental days in the MRI-scanner with intravenous infusion (hormone/placebo) and oral ingestion (glucose/water): An intravenous infusion of saline or GIP(3-30)NH2 starts at time point -20 minutes.The infusions are combined with an oral glucose tolerance test (75 gram of glucose dissolved in 250 ml water ingested orally) at time point 0 minutes on two of the experimental days (with and without GIP(3-30)NH2).
MRI measurements are repeatedly performed and blood samples are drawn to be analysed for endocrine responses from the intestines, pancreas, and bones.
Eligibility
Inclusion Criteria:
- Type 2 diabetes
- BMI 20-35 kg/m^2
- Age 20-80
Exclusion Criteria:
- Not MRI-compatible implants
- Claustrophobia
- Abnormal kidney or liver function
- Anemia
- Planned weight loss or change in diet
- Hypertension
- Other conditions that could be expected to affect the primary or secondary outcomes