Orally administered κ but not μ opiate agonists enhance gastric emptying of a solid canned food meal in dogs

Publisher Website
Google Scholar
Abstract
— The effects of oral administration of selective mu (D‐Ala2, N‐Me‐p‐nitro‐Phe4 Gly5‐ol‐DAGO, morphine) and/or kappa (3,4 dichloro‐N‐methyl N [2‐(1. fyrrolidinyl) cyclohexyl]‐benzene acetamide‐U‐50488, tifluadom) or mixed agonist (N‐desmethyltrimebutine) opioid on gastric emptying have been evaluated using a radiolabeled [57Co] canned food meal in dogs fitted with gastric cannulas. In control conditions (placebo) the percentage of solids emptied 1 h after feeding was 27.3 ± 41%. When given orally at doses of 0.01 to 0.5 mg kg−1, U‐50488 increased significantly (P < 0.05) by 29.1 to 60.8% in a dose‐related manner (r −0.94, P < 0.01) the amount of gastric emptying of the meal in 1 h. This effect was reproduced by oral administration of tifluadom (0.01 to 0.1 mg kg−1)and by N‐desmethyltrimebutine (0.1 to 1 mg kg−1). In contrast, the gastric emptying was unaffected by DAGO and morphine at low doses (0.01 and 0.1 mg kg−1) but significantly (P < 0.05) slowed with higher doses of morphine. The increases in amount of gastric emptying induced by tifluadom, U‐50488 and N‐desmethyltrimebutine were abolished by previous administration of naloxone (0.1 mg kg−1 i.v.) and [(3‐furylmethyl) noretazocine]‐MR 22–66 (0.1 mg kg−1 i.v.). These results indicate that orally administered kappa, but not mu agonists at doses not exceeding 1 mg kg−1 enhance the amount of gastric emptying of a solid meal in dogs and suggest that this is due to a selective local stimulation of kappa mucosal or submucosal opiate receptors at antroduodenal level.