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Oral administration of glucagon-like peptide 1 or peptide YY 3-36 affects food intake in healthy male subjects
Plain-language guide to PMID 20720259 (2010): double-blind randomized controlled trial study of Peptide YY.
Key Facts
- PMID
- 20720259
- Journal
- The American journal of clinical nutrition
- Year
- 2010
- Study type
- Randomized Controlled Trial
- Authors
- Steinert RE et al. (5 authors)
- DOI
- 10.3945/ajcn.2010.29663
What This Study Did, in Plain Language
What Was Tested
Researchers studied Peptide YY in this randomized controlled trial publication.
In contrast with peripheral infusion, oral delivery of sodium N-[8-(2-hydroxybenzoyl) amino] caprylate (SNAC) mimics endogenous secretion.
The researchers aimed to investigate how this affects food intake.
Why It Was Studied
In vivo, both peptides are cosecreted from intestinal L cells; GLP-1 is subject to rapid breakdown by dipeptidyl peptidase IV, and together with PYY3-36 it is likely to be degraded in the liver before entering the systemic circulation.
The largest concentrations are observed in the splanchnic blood rather than in the systemic circulation.
Who Took Part
By PubMed's age tags, the people studied were young adults and adults, men only.
The placebo treatment was the delivery agent alone.
How the Study Was Run
In design terms this was a randomized, double-blind, placebo-controlled and crossover study.
Because people in this Peptide YY study were split into groups at random, differences between the groups are less likely to reflect who happened to join each one.
Neither the participants nor the staff measuring them knew who was on Peptide YY, so expectations could not easily colour the readings.
A placebo (an inactive look-alike) gave the Peptide YY group a baseline to be compared against.
In the crossover set-up each of the participants took both Peptide YY and the comparison in turn, acting as their own control.
Food intake during an ad libitum test meal was measured.
What Was Measured
In vivo, both peptides are cosecreted from intestinal L cells; GLP-1 is subject to rapid breakdown by dipeptidyl peptidase IV, and together with PYY3-36 it is likely to be degraded in the liver before entering the systemic circulation.
The subject headings attached to it are Eating, Energy Metabolism, Glucagon-Like Peptide 1, Hunger, Peptide Fragments, Peptide YY and Satiation.
What This Means in Plain Language
The paper is a randomized, double-blind and placebo-controlled study of Peptide YY.
The abstract goes on to report its results in about 5 sentences; this page does not restate them, so read the paper for the findings and their limits.
The publication is from 2010 (The American journal of clinical nutrition), a journal based in United States.
More context: the Peptide YY compound page, all human trials.
Our Notes on the Compound
Peptide YY: A 36-amino-acid gut hormone released after eating that is studied for its role in appetite.
Related Pages
Source: PubMed record. This explanation is written by PeptideWhiz from the public record. For research and education only. Not medical advice; no dosing information is given.