Mechanisms underlying the laxative effect of lactulose: A randomized placebo‐controlled trial showing increased small bowel water and motility unaltered by the 5‐HT3 receptor antagonist, ondansetron

Author:

Gunn D.12ORCID,Yeldho C.12,Hoad C.13,Menys A.4,Gowland P.13,Marciani L.12,Spiller R.12ORCID

Affiliation:

1. NIHR Nottingham Biomedical Research Centre Nottingham UK

2. Nottingham Digestive Diseases Centre University of Nottingham Nottingham UK

3. Sir Peter Mansfield Imaging Centre University of Nottingham Nottingham UK

4. Division of Medicine, Centre for Medical Imaging University College London London UK

Abstract

AbstractBackgroundLactulose is a laxative which accelerates transit and softens stool. Our aim was to investigate its mechanism of action and use this model of diarrhea to investigate the anti‐diarrheal actions of ondansetron.MethodsA double‐blind, randomized, placebo‐controlled crossover study of the effect of ondansetron 8 mg in 16 healthy volunteers. Serial MRI scans were performed fasted and 6 h after a meal. Participants then received lactulose 13.6 g twice daily and study drug for a further 36 h. On Day 3, they had further serial MRI scans for 4 h. Measurements included small bowel water content (SBWC), colonic volume, colonic gas, small bowel motility, whole gut transit, and ascending colon relaxation time (T1AC), a measure of colonic water content.Key ResultsLactulose increased area under the curve (AUC) of SBWC from 0 to 240 min, mean difference 14.2 L · min (95% CI 4.1, 24.3), p = 0.009, and substantially increased small bowel motility after 4 h (mean (95% CI) 523 (457–646) a.u. to 852 (771–1178) a.u., p = 0.007). There were no changes in T1AC after 36 h treatment. Ondansetron did not significantly alter SBWC, small bowel motility, transit, colonic volumes, colonic gas nor T1AC, with or without lactulose.Conclusion & InferencesLactulose increases SBWC and stimulates small bowel motility; however, unexpectedly it did not significantly alter colonic water content, suggesting its laxative effect is not osmotic but due to stimulation of motility. Ondansetron's lack of effect on intestinal water suggests its anti‐diarrheal effect is not due to inhibition of secretion but more likely altered colonic motility.

Funder

University of Nottingham

Publisher

Wiley

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