The goal of this double-blinded, randomized cross-over clinical trial is to assess the isolated (i.e. outside the context of exercise) effects of Lac-Phe on appetite and glucose concentrations in healthy volunteers with obesity (BMI 28-35). The main questions it aims to answer are: * Does Lac-Phe reduce appetite in humans? * Does Lac-Phe have glucose-lowering properties in humans? During the study, participants will: * receive an intravenous infusion of Lac-Phe on one study day and a NaCl infusion on another study day. * drink a standard mixed meal * eat an ad libitum meal test * answer appetite questionnaires * indirect calorimetry * blood samples for hormone and substate analyses
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
OTHER
Masking
DOUBLE
Enrollment
23
Intravenous infusion of N-lactoyl-phenylalanine (Lac-Phe)
0.9% isotonic NaCl infusion
SDCA research laboratory
Aarhus N, Denmark
ad libitum meal test
Meal intake (kcal) during the ad libitum meal test
Time frame: On the study day, from times 240 minutes and until meal completion as assessed by study participant
Lac-phe
plasma concentrations of lac-phe
Time frame: During the study day, time 0-240 minutes
glucose
plasma concentrations of glucose
Time frame: During the study day, time 0-240 minutes
lactate
plasma concentrations of lactate
Time frame: During the study day, time 0-240 minutes
c-peptide
serum concentrations of c-peptide
Time frame: During the study day, time 0-240 minutes
triglycerider
plasma concentrations of triglycerides
Time frame: During the study day, time 0-240 minutes
GLP-1
plasma concentration of GLP-1
Time frame: During the study day, time 0-240 minutes
GIP
plasma concentrations of GIP
Time frame: During the study day, time 0-240 minutes
Ghrelin
plasma concentration of ghrelin
Time frame: During the study day, time 0-240 minutes
insulin
serum concentration of insulin
Time frame: During the study day, time 0-240 minutes
free fatty acids
Serum concentrations of free fatty acids
Time frame: During the study day, time 0-240 minutes
LEAP2
Plasma concentration of liver-expressed antimicrobial peptide 2 (LEAP2)
Time frame: From baseline to end of study day (time 0-240 minutes)
Glucagon
Plasma concentration of glucagon
Time frame: From baseline to end of study day (time 0-240 minutes)
Gastric emptying assessed by acetaminophen
Plasma concentration of acetaminophen following oral acetaminophen intake
Time frame: From baseline to end of study day (time 0-240 minutes)
Subjective appetite - appetite questionaire
We will assess subjective appetite sensations on a visual analog score. Scale range from 1 to 10 centimeters.
Time frame: Hourly thoughout the study - times 0, 60, 120, 180 and 240 minutes
Energy expenditure
Indirect calorimetry
Time frame: After 60 and approx 180 minutes
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