Abstract.
In intact tissue, DAGO ([D-Ala2, MePhe4, Gly-ol5]enkephalin; 10−5 M; μ-ligand; addition on the serosal side) stimulated D-glucose absorption and D-glucose-dependent variations in short-circuit current (ΔIsc,glu); naloxone (10−6 M) antagonized these effects. DADLE ([D-Ala2, D-Leu5]enkephalin, mainly a δ-ligand; 10−5 M) and (pCl-Phe4)-DPDPE ([D-pen2, p-chloro-Phe4, D-Pen5]enkephalin, a more selective δ-ligand; 10−5 M) did not significantly stimulate ΔIsc,glu (addition on the serosal side). In the absence of the muscularis and myenteric plexus or using intact tissue treated with tetrodotoxin (TTX; 3×10−7 M), DAGO was unable to increase ΔIsc,glu . Addition of DAGO to the mucosal side did not induce any variations in ΔIsc,glu . In conclusion, DAGO is able to increase D-glucose absorption by interacting with μ-receptors located in the myenteric plexus.
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Received 15 May 1997; received after revision 28 July 1997; accepted 31 July 1997
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Meyer, G., Bottà, G. & Cremaschi, D. Stimulation by enkephalins of D-glucose absorption in rabbit ileum. CMLS, Cell. mol. life sci. 53, 769–775 (1997). https://doi.org/10.1007/s000180050097
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DOI: https://doi.org/10.1007/s000180050097