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CompletedNCT01304823Updated Jul 16, 2015

Role of the Gut Sweet Taste Receptor in the Secretion of Glucagon-like Peptide-1 and Peptide YY

A Phase 1 interventional study of lactisole and mixed liquid meal in Taste Disorder, Primary, Sweet, sponsored by University Hospital, Basel, Switzerland. Completed at 1 site in Switzerland. Open to male participants aged 18 Years to 40 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2015-07-16.

Sponsored by University Hospital, Basel, Switzerland · Phase 1, Interventional, and Basic science

Phase
Phase 1
Study type
Interventional
Enrollment
10
Allocation
Randomized
Ages
18 Years to 40 Years
Sex
Male
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Study summary

The purpose of this study is to determine the functional significance of sweet taste receptors in the secretion of GI satiation peptides by using a specific sweet taste receptor antagonist to block sweet taste perception in the gastrointestinal tract.

Read the detailed description

There is strong evidence that taste signaling mechanisms identified in the oral epithelium also operate in the gut. It is suggested that open-type enteroendocrine cells directly sense nutrient via alpha-gustducin coupled taste receptors to modulate the secretion of glucagon like peptide-1 (GLP-1) and peptide YY (PYY). Several nutrient responsive G-protein coupled receptors have been identified in the human gut, including the sweet taste responsive T1R2/T1R3 heterodimer, the amino acid/umami responsive T1R1/T1R3 as well as GPR120 for unsaturated long-chain free fatty acids.The functional significance of sweet taste receptors in the secretion of GLP-1 and PYY will be determined by intraduodenal perfusion of glucose (I) or a mixed liquid meal (II) with or without lactisole (450 ppm) in a double blind, 5-way crossover trial including 10 healthy subjects.

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Conditions studied

  • Taste Disorder, Primary, Sweet

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Keywords

  • T1R2/T1R3
  • gastric emptying
  • gut
  • lactisole
  • nutrient sensing
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In context

Taste Disorders

40 studies on the registry are indexed under Taste Disorders; 6 are open to participants now.

This study's enrollment of 10 is below the median of 64 across 18 interventional studies indexed under Taste Disorders.

Browse Taste Disorders studies →

Lead sponsor

University Hospital, Basel, Switzerland is the lead sponsor of 968 studies on the registry; 191 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 40 Years
Sexes eligible
Male
Accepts healthy volunteers
Yes

Inclusion criteria

  • Healthy subjects
  • BMI of 19.0-24.5
  • Age 18-40
  • stable body weight for at least 3 month

Exclusion criteria

Exclusion Criteria:

  • smoking
  • substance abuse
  • regular intake of medication
  • medical or psychiatric illness
  • gastrointestinal disorders or food allergies
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Study design

Phase
Phase 1
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
10 participants (actual)

Study arms

  • Active comparator
    glucose

    intraduodenal perfusion of glucose (29.3 g glucose per 100 mL; rate: 2.5 mL/min for 180 min; caloric load: 3.0 kcal/min)

    Dietary Supplement: lactisole

  • Active comparator
    glucose + lactisole

    intraduodenal perfusion of glucose (29.3 g glucose per 100 mL; rate: 2.5 mL/min for 180 min; caloric load: 3.0 kcal/min) + 450 ppm lactisole

    Dietary Supplement: lactisole

  • Active comparator
    mixed liquid meal

    intraduodenal perfusion of a mixed liquid meal (20.20 g carbohydrate, 4.92 g fat and 6.25 g protein per 100 mL; rate: 2.5 mL/min for 180 min; caloric load: 3.0 kcal/min)

    Other: mixed liquid meal

  • Active comparator
    mixed liquid meal + lactisole

    intraduodenal perfusion of a mixed liquid meal (20.20 g carbohydrate, 4.92 g fat and 6.25 g protein per 100 mL; rate: 2.5 mL/min for 180 min; caloric load: 3.0 kcal/min) + 450 ppm lactisole

    Other: mixed liquid meal

  • Placebo comparator
    saline + lactisole

    saline (0.9 %; rate: 2.5 mL/min for 180 min) + 450 ppm lactisole

    Dietary Supplement: lactisole

Interventions

  • Dietary supplementlactisole

    flavoring agent/sweet taste antagonist

    Also known as: Dietary supplement

  • Othermixed liquid meal

    Ensure Plus

    Also known as: Dietary supplement

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What researchers measure

Primary outcomes

  1. Gastrointestinal peptide secretion

    Assessment of venous GLP-1 and PYY release to meal stimulation with and without sweet receptor blockade

    Time frame: 4 hours blood sampling

Secondary outcomes

  1. Appetite perceptions during 4 hours using VAS

    Assessment of the following appetite perception markers: feelings of hunger, feelings of fullness, feelings of satiety using validated visual analogue scales

    Time frame: 4 hours

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Study locations

1 site
  • University Hospital Basel, Phase 1 Research Unit
    Basel, 4031, Switzerland
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References and documents

Publications

  • Steinert RE, Meyer-Gerspach AC, Beglinger C. The role of the stomach in the control of appetite and the secretion of satiation peptides. Am J Physiol Endocrinol Metab. 2012 Mar 15;302(6):E666-73. doi: 10.1152/ajpendo.00457.2011. Epub 2012 Jan 3. PubMed 22215654 ↗
  • Steinert RE, Gerspach AC, Gutmann H, Asarian L, Drewe J, Beglinger C. The functional involvement of gut-expressed sweet taste receptors in glucose-stimulated secretion of glucagon-like peptide-1 (GLP-1) and peptide YY (PYY). Clin Nutr. 2011 Aug;30(4):524-32. doi: 10.1016/j.clnu.2011.01.007. Epub 2011 Feb 15. PubMed 21324568 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 16, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT01304823
Lead sponsor
University Hospital, Basel, Switzerland
Responsible party
Sponsor
First posted
Feb 25, 2011
Start date
Jun 2010
Primary completion
Aug 2010
Completion
Jan 2011
Last update
Jul 16, 2015

Study contacts

Christoph Beglinger, MD
principal investigator · Phase 1 Research Unit, University Hospital Basel

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jul 2015. You cannot join it, but the record below documents what was studied.

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