"Effect of Central Insulin Administration on Whole-body Insulin Sensitivity in Women"

Sponsor
University Hospital Tuebingen (Other)
Overall Status
Completed
CT.gov ID
NCT03929419
Collaborator
(none)
29
1
2
24.3
1.2

Study Details

Study Description

Brief Summary

The human brain is an insulin sensitive organ. Brain insulin action modulates peripheral insulin sensitivity in young lean men. As a underlying mechanism, the investigators previously detected suppression of endogenous glucose production and stimulation of glucose disappearance to peripheral tissue in response to brain insulin delivery by nasal spray. Whether this holds true in young woman is unknown, since differences in brain insulin response between sexes have been reported. The investigators will address this question by combining the delivery of insulin to the brain as nasal spray with hyperinsulinemic euglycemic clamp experiments in natural cycling women.

In the planned randomized, placebo controlled cross-over study, female participants will undergo four hyperinsulinemic euglycemic experiments with tracer dilution, two in the first phase and two in the second phase of their menstrual cycle. On one of the study days per menstrual phase, subjects will receive intranasal insulin administration, on the other placebo spray. The protocol has been successfully applied previously in men. Based on the results of this trial, the investigators calculated a required sample size of N=10 for the planned study in women.

These experiments will help to better understand the role of brain insulin action in a broader sense. The results can be the basis for larger clinical trials that address the sex-specific impact of brain insulin resistance for glucose metabolism and diabetes risk.

Condition or Disease Intervention/Treatment Phase
  • Drug: intranasal insulin
  • Drug: Placebo spray
N/A

Detailed Description

"Effect of central insulin administration on whole-body insulin sensitivity in women" The human brain is an insulin sensitive organ. Brain insulin action modulates peripheral insulin sensitivity in young lean men. As a underlying mechanism, the investigators previously detected suppression of endogenous glucose production and stimulation of glucose disappearance to peripheral tissue in response to brain insulin delivery by nasal spray. Whether this holds true in young woman is unknown, since differences in brain insulin response between sexes have been reported. The investigators will address this question by combining the delivery of insulin to the brain as nasal spray with hyperinsulinemic euglycemic clamp experiments in natural cycling women.

In the planned randomized, placebo controlled cross-over study, female participants will undergo four hyperinsulinemic euglycemic experiments with tracer dilution, two in the first phase and two in the second phase of their menstrual cycle. On one of the study days per menstrual phase, subjects will receive intranasal insulin administration, on the other placebo spray. The protocol has been successfully applied previously in men. Based on the results of this trial, the investigators calculated a required sample size of N=10 for the planned study in women.

These experiments will help to better understand the role of brain insulin action in a broader sense. The results can be the basis for larger clinical trials that address the sex-specific impact of brain insulin resistance for glucose metabolism and diabetes risk.

Study Design

Study Type:
Interventional
Actual Enrollment :
29 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
Single (Participant)
Primary Purpose:
Basic Science
Official Title:
"Effect of Central Insulin Administration on Whole-body Insulin Sensitivity in Women"
Actual Study Start Date :
Apr 21, 2019
Actual Primary Completion Date :
Mar 25, 2021
Actual Study Completion Date :
Apr 30, 2021

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Insulin nasal spray

160 Units of human insulin as nasal spray

Drug: intranasal insulin
application of 160 units human insulin

Placebo Comparator: Placebo nasal spray

Nasal spray containing placebo solution

Drug: Placebo spray
nasal spray containing placebo solution

Outcome Measures

Primary Outcome Measures

  1. Change in the peripheral insulin sensitivity [60-90 minutes and 150-210 minutes during euglycemic clamp]

    Effect of nasal insulin versus placebo on peripheral insulin sensitivity assessed by euglycemic hyperinsulinemic clamp.

Secondary Outcome Measures

  1. Correlation with autonomous nervous system activity [70-80 minutes and 190-200 minutes during euglycemic clamp]

    Correlation of the change in peripheral insulin sensitivity by central insulin action with the simultaneous change of the autonomous nervous system (measured by heart rate variability).

  2. Differential effects dependent on female sexual hormones [60-90 minutes and 150-210 minutes during euglycemic clamp]

    Correlation of the change in peripheral insulin sensitivity by central insulin action dependent on the time point in menstrual cycle

  3. Effect of menstrual cycle on insulin sensitivity before spray application [60-90minutes]

    Will be measured by hyperinsulinemic euglycemic clamp

  4. Effect of menstrual cycle on brain insulin sensitivity [60-90 minutes]

    Brain insulin sensitivity will be assessed by functional magnetic resonance imaging combined with intranasal insulin administration during the follicular and the luteal phase of the menstrual cycle

  5. Effect of menstrual cycle on processing of food cues in the brain [20 minutes]

    Processing of food cues in the brain will be assessed by functional magnetic resonance imaging during the follicular and the luteal phase of the menstrual cycle

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 30 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • female volunteer adults

  • HbA1c <6.0%

  • Age between 18 and 30 years

  • Standard routine laboratory

  • No underlying diseases

  • No medication

  • No hormonal contraception

  • Understanding of the explanations of the study and the instructions

Exclusion Criteria:
  • Persons with limited temperature perception and / or increased temperature Sensitivity to warming of the body

  • Cardiovascular disease, such as manifest coronary Heart disease, heart failure greater than NYHA 2, recent myocardial infarction

  • People with a hearing disorder or increased sensitivity to loud Sounds

  • persons with claustrophobia

  • Minors or non-consenting subjects are also excluded

  • Pregnancy or breastfeeding women

  • Surgery less than 3 months ago

  • Simultaneous participation in other interventional studies

  • Acute illness or infection within the last 4 weeks

  • Neurological and psychiatric disorders

  • Subjects with hemoglobin Hb <12g / dl (at screening)

  • Allergic diseases

  • Individuals with a history of heparin-induced thrombocytopenia (HIT)

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Tuebingen, Department of Internal Medicine IV Tuebingen Germany 72076

Sponsors and Collaborators

  • University Hospital Tuebingen

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University Hospital Tuebingen
ClinicalTrials.gov Identifier:
NCT03929419
Other Study ID Numbers:
  • 568/2018BO1
First Posted:
Apr 26, 2019
Last Update Posted:
Sep 5, 2021
Last Verified:
Nov 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 5, 2021