Publikation

Gut protein uptake and mechanisms of meal-induced cortisol release

Wissenschaftlicher Artikel/Review - 01.03.2005

Bereiche
PubMed
DOI

Zitation
Benedict C, Hallschmid M, Scheibner J, Niemeyer D, Schultes B, Merl V, Fehm H, Born J, Kern W. Gut protein uptake and mechanisms of meal-induced cortisol release. The Journal of clinical endocrinology and metabolism 2005; 90:1692-6.
Art
Wissenschaftlicher Artikel/Review (Englisch)
Zeitschrift
The Journal of clinical endocrinology and metabolism 2005; 90
Veröffentlichungsdatum
01.03.2005
ISSN (Druck)
0021-972X
Seiten
1692-6
Kurzbeschreibung/Zielsetzung

The enhanced cortisol release after protein-rich meals might represent a neuroendocrine response to food allergens. We tested whether the antigenicity of proteins contributes to this effect. Twelve healthy men nasogastrically received casein, its less allergenic hydrolysate, and placebo. Contrary to expectations, secretion of cortisol (area under the curve, 742.70 +/- 73.48 vs. 542.95 +/- 70.31 micromol/liter.min, P < 0.03) and ACTH (2020.21 +/- 251.10 vs. 1649.82 +/- 241.23 micromol/liter.min, P < 0.05) was stronger on casein-hydrolysate than casein. Systemic immune activity remained unaffected as indicated by unchanged IL-6 plasma concentrations. This finding indicates that the grade of hydrolysis of a protein and the presence of particular amino acids, rather than its antigenicity, are crucial for the pituitary-adrenal response to nutrients. To further examine whether this response is triggered at the gastrointestinal mucosa or after the substance has reached the circulation, in a supplementary experiment, amino acids were given either nasogastrically or iv to healthy men (n = 4). Only the nasogastric infusion of amino acids induced a significant rise in cortisol concentrations. Serum concentrations of tryptophan, which is known to directly excite the hypothalamo-pituitary-adrenal axis, were comparable for both conditions. We conclude that the meal-related hypothalamo-pituitary-adrenal axis response to amino acids results from a signal that rather acts at the gastrointestinal mucosa than directly via the circulating blood.