Abstract Title:

Intravenous administration of the food-derived opioid peptide gluten exorphin B5 stimulates prolactin secretion in rats.

Abstract Source:

Pharmacol Res. 2003 Jan ;47(1):53-8. PMID: 12526862

Abstract Author(s):

Giuseppe Fanciulli, Alessandra Dettori, Emma Fenude, Maria Piera Demontis, Elisabetta Alberico, Giuseppe Delitala, Vittorio Anania

Article Affiliation:

Dipartimento-Struttura Clinica Medica-Patologia Speciale Medica, Istituto di Patologia Medica, University of Sassari, Viale San Pietro 8, 07100 Sassari, Italy. [email protected]


Gluten Exorphin B5 (GE-B5) is a food-derived opioid peptide, identified in vitro in enzymatic digests of wheat gluten. It has been suggested that this peptide may play a regulatory role on pituitary secretion, since it stimulates prolactin (PRL) secretion when administered in the cerebral ventricles in rats. It is not known, however, if GE-B5 can exert this stimulatory action after peripheral administration. In order to clarify this aspect, we gave the following treatments to four groups of male rats: intravenous (i.v.) vehicle, GE-B5 3 mg/kg body weight i.v., naloxone intraperitoneally (i.p.) followed by vehicle i.v., naloxone i.p. followed by GE-B5 i.v. Blood samples for PRL were taken at intervals for 60 min after vehicle or GE-B5 administration. At the dose of 3 mg/kg body weight, GE-B5 induced a significant increase in PRL levels; naloxone completely abolished any effect of GE-B5 on PRL secretion. The present study indicates that GE-B5 stimulates PRL secretion after peripheral administration and that its action is mediated via classical opioid receptors; moreover, it identifies the minimum peptide dose which must reach the blood in order to exert its action on PRL secretion.

Study Type : Animal Study

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