The Effect of GLP-1 on Glucose Uptake in the Brain and Heart in Healthy Men During Hypoglycemia

Sponsor
University of Aarhus (Other)
Overall Status
Completed
CT.gov ID
NCT00418288
Collaborator
(none)
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Study Details

Study Description

Brief Summary

Type 2 diabetes mellitus, T2D is a disease characterized by an immense growing prevalence world wide with an increased risk of myocardial infarction and stroke. GLP-1 has convincing effects on the high glucose levels in type 2 diabetic patients and is well tolerated. New animal studies indicate a protective effect of GLP-1 in the brain and the heart. The mechanism behind this is yet not known.

The study hypothesis is that during hypoglycaemia GLP-1 will stimulate glucose-uptake in the brain and heart independent of insulin and thereby exert protective effects in the brain.

Condition or Disease Intervention/Treatment Phase
N/A

Detailed Description

Type 2 diabetes mellitus, T2D is a disease characterized by an immense growing prevalence world wide. T2D is associated with a three-fold increase in cardiovascular complications (myocardial infarction and stroke) leading to significantly higher morbidity and mortality in this group of patients. The prospective British Diabetes Study (UKPDS) showed that neither diet alone nor the pharmaceutical treatment utilized (Sulphonylurea, Metformin, Insulin) were able to reduce these macrovascular complications. GLP-1 (glucagon-like-peptide-1)is an incretin with convincing effects on glycaemia in type 2 diabetic patients with little or no risk of hypoglycaemia. New research in animal models has shown a potential protective effect in the brain and heart in association with ischaemic damage. The mechanism behind this protective effect is not known. During hypoglycaemia the brain lacks glucose which is the main fuel for sufficient brain function. The brain will compensate by increasing glucose uptake across the blood brain barrier and similarly in the heart.

The effect of native GLP-1 on glucose uptake in the brain and heart will by visualized by fluoro-deoxy-glucose FDG-PET-scan during hypoglycaemia in healthy men. At the same time a pancreatic/pituitary clamp will be performed. The hypothesis is that GLP-1 directly will stimulate glucose uptake independent of the pancreatic hormones and through this mechanism exert neuro- and cardioprotective actions.

Comparisons: FDG-uptake in the brain and heart with GLP-1 infusion compared to placebo.

Study Design

Study Type:
Interventional
Actual Enrollment :
10 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
The Effect of GLP-1 on Glucose Uptake in the Brain and Heart in Healthy Subjects During Hypoglycemia Assessed by Positron Emission Tomography
Study Start Date :
Jan 1, 2007
Actual Primary Completion Date :
Oct 1, 2007
Actual Study Completion Date :
Feb 1, 2008

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: A

Drug: glucagon-like-peptide-1
intravenous infusion of 1.2pmol/kg/min for 7 hours

Placebo Comparator: P

Drug: placebo
intravenous infusion of 1.2pmol/kg/min

Outcome Measures

Primary Outcome Measures

  1. The acute effect of GLP-1 on glucose uptake in the brain [1 hour]

  2. The acute effect of GLP-1 on glucose uptake in the heart [1 hour]

Secondary Outcome Measures

  1. The acute effect of GLP-1 on glucose metabolic rate in the brain [1 hour]

  2. The acute effect of GLP-1 on intracerebral glucose concentration [1 hour]

  3. The acute effect of GLP-1 on lumped constant in the brain [1 hour]

Eligibility Criteria

Criteria

Ages Eligible for Study:
20 Years to 50 Years
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Healthy men

  • Age 20-50 years

  • Caucasian

  • BMI 20-30 kg/m2

Exclusion Criteria:
  • Diabetes in subject and 1.degree relatives

  • Any disease of clinical relevance

Contacts and Locations

Locations

Site City State Country Postal Code
1 Department of pharmacology, Aarhus university Aarhus Denmark 8000

Sponsors and Collaborators

  • University of Aarhus

Investigators

  • Principal Investigator: Ole E Schmitz, MD, DSc, Department of pharmacology, Aarhus university

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00418288
Other Study ID Numbers:
  • 2005-0089
First Posted:
Jan 4, 2007
Last Update Posted:
Jun 10, 2008
Last Verified:
Jun 1, 2008

Study Results

No Results Posted as of Jun 10, 2008