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Hyperglycemia and the Extra-pancreatic Effect of Incretins

Determining the Extra-pancreatic Effects of Incretin Hormones During Euglycemic and Hyperglycemic Pancreatic Clamps

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01749163
Enrollment
20
Registered
2012-12-13
Start date
2012-09-30
Completion date
2014-03-31
Last updated
2014-12-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Extra-pancreatic Incretin Effect, Glucose Effectiveness

Brief summary

Incretin hormones (GLP-1 and GIP) released from the intestine in response to meal ingestion augment insulin secretion from the pancreas to help maintain glycemic control. Studies in vitro and in vivo have shown that these incretin hormones also have functional effects in other tissues independent of the insulin secretory response. Both GLP-1 and GIP stimulate insulin secretion in a glucose-dependent manner, however the glucose-dependency of their extra-pancreatic effects has not been examined in vivo. By using pancreatic clamp methodology during euglycemic and hyperglycemic conditions we will test the hypothesis that extra-pancreatic effects of GLP-1 and GIP are glucose-dependent.

Interventions

BIOLOGICALSaline
BIOLOGICALGIP
BIOLOGICALGLP-1

Sponsors

Rigshospitalet, Denmark
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* age 18-60 years * BMI 18-30 kg/m2 * Male * Normal glycemic control (fasting glucose \<5.6 mM)

Exclusion criteria

* Evidence of chronic disease * Smoking * Active weight loss (\>2 kg in previous 6 months) * Treatment with drugs known to affect our outcome varaibles

Design outcomes

Primary

MeasureTime frameDescription
Glucose metabolismup to 4 hoursPancreatic clamp will be performed including infusion of somatostatin and replacement of basal insulin, glucagon, and growth hormone. During pancreatic clamps, euglycemia (5 mM) will be maintained via exogenous glucose infusion for the first 2-hours, followed by hyperglycemia (+5 mM) for the final 2-hours. An infusion of the stable isotope \[U13C\]glucose will be performed to assess glucose kinetics. Expired air will be collected for the analysis of \[U13C\]glucose into 13CO2.
Lipid metabolismup to 4 hoursAn infusion of the stable isotope \[D5\]glycerol will be performed to assess glycerol kinetics.

Secondary

MeasureTime frameDescription
Endothelial functionBaseline, 2 hours, and 4 hoursUltrasound Doppler will be used to examine lower and upper limb blood flow and flow-mediated dilation
SignalingBaseline, 2 hours, and 4 hoursSkeletal muscle (vastus lateralis) and subcutaneous abdominal adipose biopsies will be obtained under local anaesthetic by the Bergstrom needle technique. Intracellular signalling related to glucose and lipid metabolism will be measured.

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026