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Clinical Trials/NCT03590561
NCT03590561CompletedNot Applicable

Einfluss Von Hochkalorischer Nahrungsaufnahme Auf Die Insulinsensitivität Des Menschlichen Zentralnervensystems

University Hospital Tuebingen1 site in 1 country32 target enrollmentStarted: June 13, 2018Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
32
Locations
1
Primary Endpoint
Change in brain metabolites

Study Overview

Brief Summary

Obesity if known to be associated with brain insulin resistance in humans and evidence is rapidly accumulating that brain insulin resistance influences peripheral metabolism, eating behavior and cognition. A reduced insulin response in the brain is found mainly in people with a metabolically unfavorable fat distribution - high visceral fat. Visceral fat produces inflammatory mediators and elevated inflammatory levels are closely linked to insulin resistance. Inflammation of the brain (i.e., neuroinflammation) has been proposed as a possible cause of brain insulin resistance. Interestingly, rodent models of a high calorie diet show that these inflammatory mechanisms occur rapidly in the brain, even prior to weight gain of the animals. Among other things, it has been shown in humans that a short-term increase in calories, especially carbohydrates and fats, reduces insulin sensitivity in the body and increases inflammatory parameters in the blood. Whether a high-calorie diet triggers insulin resistance or inflammation in the human brain is currently unknown.

Aim of study:

The aim of the study is to investigate the effects of a five-day high calorie diet in healthy young male volunteers on peripheral and brain insulin sensitivity as well as on eating behavior, mood and cognition. Brain insulin sensitivity, peripheral metabolism and different behavioral assessments will be evaluated before, 1 week and 2 weeks after high caloric diet.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Sequential
Primary Purpose
Basic Science
Masking
None

Eligibility Criteria

Ages
18 Years to 29 Years (Adult)
Sex
Male
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •BMI 19-24 kg/m2
  • •Non smoking
  • •normal glucose tolerance during 75g oral glucose tolerance test (OGTT)
  • •Exercise less than 2h per week

Exclusion Criteria

  • •Vegetarians and Vegans
  • •Food allergies
  • •Working at night
  • •Professional Athletes
  • •Not removable metal parts in or on the body
  • •manifest cardiovascular disease
  • •claustrophobia
  • •recent surgery (less than 3 months)
  • •Simultaneous participation in other studies
  • •Acute disease or infection within the last 4 weeks
  • •neurological and psychiatric disorders
  • •treatment with centrally acting drugs
  • •hemoglobin Hb <13g / dl
  • •Hypersensitivity to any of the substances used

Arms & Interventions

High caloric diet

Experimental

Participants will eat 1500 kcal more than their usual diet for five days.

Intervention: High caloric diet (Other)

Control diet

No Intervention

Participants will eat regular diet.

Outcomes

Primary Outcomes

Change in brain metabolites

Time Frame: Outcome measurements will be assessed at baseline (t0). Then, the 5-day high caloric diet or control dietwill start 5 to 30 days after t0. Outcome measurements will again be assessed on the 6th-7th day and on the 10th-15th day after start of diet.

The inflammatory processes in the brain will be measured through the determination of brain metabolites by MR spectroscopy

Change in brain insulin sensitivity

Time Frame: Outcome measurements will be assessed at baseline (t0). Then, the 5-day high caloric diet or control dietwill start 5 to 30 days after t0. Outcome measurements will again be assessed on the 6th-7th day and on the 10th-15th day after start of diet.

fMRI measurement will be performed before and after administration of 160 U of human insulin as nasal spray. Changes in regional activity will be quantified to assess regional brain insulin sensitivity.

Change in quantitative proton density

Time Frame: Outcome measurements will be assessed at baseline (t0). Then, the 5-day high caloric diet or control dietwill start 5 to 30 days after t0. Outcome measurements will again be assessed on the 6th-7th day and on the 10th-15th day after start of diet.

The inflammatory processes in the brain will be measured through the quantification of the water content by means of proton density imaging.

Secondary Outcomes

  • Change in whole-body insulin sensitivity(Outcome measurements will be assessed at baseline (t0). Then, the 5-day high caloric diet or control diet will start 5 to 30 days after t0. Outcome measurements will again be assessed on the 6th-7th day and on the 10th-15th day after start of diet.)
  • Behavioral assessment(Outcome measurements will be assessed at baseline (t0). Then, the 5-day high caloric diet or control dietwill start 5 to 30 days after t0. Outcome measurements will again be assessed on the 6th-7th day and on the 10th-15th day after start of diet.)
  • Change in insulin secretion(Outcome measurements will be assessed at baseline (t0). Then, the 5-day high caloric diet or control dietwill start 5 to 30 days after t0. Outcome measurements will again be assessed on the 6th-7th day and on the 10th-15th day after start of diet.)
  • Change in body fat distribution(Outcome measurements will be assessed at baseline (t0). Then, the 5-day high caloric diet or control dietwill start 5 to 30 days after t0. Outcome measurements will again be assessed on the 6th-7th day and on the 10th-15th day after start of diet.)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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