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Intact Vagal Innervation for and Glucagon-like Peptide-1 (GLP-1) Effects

The Significances of Intact Vagal Innervation for the Glucose and GLP1 Induced Insulin Secretion

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01176760
Enrollment
30
Registered
2010-08-06
Start date
2009-08-31
Completion date
2012-12-31
Last updated
2012-12-07

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

Conditions

Vagotomy, Truncal

Keywords

vagotomy, vagus, GLP-1, Insulin secretion

Brief summary

The aim of this study is to investigate the role of transmission via the vagal nerve for the effect of glucose and Glucagon-like peptide-1 (GLP-1) in respect to insulin secretion. The hypothesis is that a great deal of the effects of GLP-1 is mediated via the nervous system and for this reason the investigators will research individuals with and without intact nervous supply.

Detailed description

GLP-1 is a potent enterogastron and incretin hormone. It is rapidly inactivated by dipeptidyl peptidase IV so only 10-15% enters the systemic circulation. This has led to the hypothesis that GLP-1 interact locally with afferent sensory nerve fibers. We investigated the role of intact vagal innervations on the effect of glucose and GLP-1 on the insulin secretion

Interventions

DRUGDipeptidyl peptidase 4 (DPP 4) inhibitor

One tablet (50 mg)of DPP4 inhibitor is to be taken 12 and 1 hours before start of the oral glucose tolerance test (50 g glucose and 1.5 g paracetamol dissolved in 300 ml water)on day 3

50 g glucose dissolved in 300 ml water with 1,5 g paracetamol is to be ingested orally within the first 15 minutes.

Sponsors

University of Copenhagen
CollaboratorOTHER
University Hospital, Gentofte, Copenhagen
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
Yes

Inclusion criteria

* normal fasting plasma glucose * normal hemoglobin * informed consent

Exclusion criteria

* type 1 diabetes mellitus or type 2 diabetes mellitus * body mass index \> 30 * inflammatory bowel disease * intestinal surgery * serum creatinine \> 250 µM and/or albuminuria * ALAT \> 2 x normal value * Severe cardiac insufficiency * in treatment with medicine which cannot be paused for 12 hours

Design outcomes

Primary

MeasureTime frameDescription
insulin secretionfour hoursThe insulin secretion during a four-hour oral glucose tolerance test (OGTT) and an intravenous isoglycaemic clamp is evaluated

Secondary

MeasureTime frameDescription
plasma GIP12 time points within four hours12 blood samples will be drawn during the four hours OGTT and intravenous isoglycaemic clamp, most frequently during the first hour
plasma glucagon12 time points within four hours12 blood samples will be drawn during the four hours OGTT and intravenous isoglycaemic clamp, most frequently during the first hour
plasma GLP-112 time points within four hours12 blood samples will be drawn during the four hours OGTT and intravenous isoglycaemic clamp, most frequently during the first hour
plasma GLP-212 time points within four hours12 blood samples will be drawn during the four hours OGTT and intravenous isoglycaemic clamp, most frequently during the first hour
plasma PYY12 time points within four hours12 blood samples will be drawn during the four hours OGTT and intravenous isoglycaemic clamp, most frequently during the first hour

Countries

Denmark

Outcome results

None listed

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