About this trial
This study will investigating the effects of glucagon on renal blood flow in humans using MRI technology. Glucagon, a hormone produced by the pancreas, plays a key role in regulating blood sugar levels. It has been shown to affect renal function, including electrolyte balance and blood flow, especially in conditions like type 2 diabetes where abnormal glucagon levels are common. The study aims to understand how glucagon affects regional blood flow in the kidneys, specifically the cortex and medulla, and whether these effects are mediated by glucagon receptors.
The study will be conducted on 10 healthy male participants aged 20-60 years. It involves three test days where participants will receive either glucagon, glucagon with a GLP-1 receptor antagonist, or placebo. Blood flow, glomerular filtration rate, and other renal functions will be measured using MRI. The study seeks to clarify whether glucagon's effects on the kidneys are linked to changes in regional blood flow and to determine if these effects are mediated solely by glucagon receptors.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Normal health confirmed through; Interview and Medical examination
Normal values with respect to blood concentrations of fasting plasma glucose, fasting plasma total cholesterol, fasting triglycerides, HDL, LDL, creatinine, liver function tests, and electrolytes
Informed consent
Disqualifiers
Immunosuppressive treatment in the previous 12 months
Alcohol abuse
Medical treatment with oral glucocorticoids, dipeptidyl peptidase-4 (DPP-4) inhibitors, or GLP-1 receptor agonists, which, in the opinion of the principal investigator, may interfere with glucose metabolism
Use of lithium
Trial design
Crossover
Treatments tested in this trial
Glucagon
DrugGlucagon infusion at 5 ng·kg-¹·min-¹ from 0-30 minutes and 10 ng·kg-¹·min-¹ from 30-60 minutes.
Glucagon+Exendin9-39
DrugGlucagon infusion at 5 ng·kg-¹·min-¹ from 0-30 minutes and 10 ng·kg-¹·min-¹ from 30-60 minutes, plus a GLP-1R antagonist, exendin 9-39 (900 pmol·kg-¹·min-¹), given intravenously from -30 to 60 minutes
Sodium chloride
DrugPlacebo (0.9% NaCl).
Treatment groups
Trial outcomes
Primary outcomes
Blood perfusion of the kidney
we would like to measure blood perfusion of the kidneys over time
Secondary outcomes
Blood flow of the renal arteries
blood oxygen saturation of the kidneys
Locations
Sponsors and contacts
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This trial is not recruiting at the moment. You can still explore other options: