Effect of Casein and β-Casomorphins on Gastrointestinal Motility in Rats

The effect of bovine casein and synthetic β-casomorphins on the motility of rat gastrointestinal tract was studied by noninvasive techniques using the nonabsorbable marker 141Ce. Casein suspensions (CAS) or whey protein suspensions (WPS) were labeled with 141Ce and fed by gastric tube. Gastric empty...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:The Journal of nutrition 1990-03, Vol.120 (3), p.252-257
Hauptverfasser: Daniel, Hannelore, Vohwinkel, Margret, Rehner, Gertrud
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:The effect of bovine casein and synthetic β-casomorphins on the motility of rat gastrointestinal tract was studied by noninvasive techniques using the nonabsorbable marker 141Ce. Casein suspensions (CAS) or whey protein suspensions (WPS) were labeled with 141Ce and fed by gastric tube. Gastric emptying rate (GER) as well as gastrointestinal transit time (GITT) of the tracer were significantly longer with feeding CAS compared to WPS. The differences between the CAS and the WPS groups were partly (GER) or completely (GITT) abolished by pretreating the animals with the specific opiate-receptor antagonist naloxone. It is assumed that opioid peptides released from casein during digestion slowed gastrointestinal motility by direct interaction with gut opiate receptors. To prove whether β-casomorphins, when given by gastric tube, can affect motility, different synthetic β-casomorphins in doses between 1 and 10 mg were added to the WPS. The β-casomorphin-4 (Tyr-Pro-Phe-Pro-NH2) showed no effect on GITT. The D-Ala substituted D-Ala-β-casomorphin-4 (Tyr-D-Ala-Phe-Pro-NH2) and D-Ala-β-casomorphin-5 (Tyr-D-Ala-Phe-D-Ala-Tyr-NH2), which are more resistant to proteolytic attack and have higher opioid potency than β-casomorphin-4, slowed GITT in a dose-dependent manner.
ISSN:0022-3166
DOI:10.1093/jn/120.3.252