Influence of ondansetron on gastric sensorimotor responses to short duodenal acid infusion in healthy volunteers



This article is corrected by:

  1. Errata: Corrigendum Volume 24, Issue 1, 94, Article first published online: 21 December 2011

Address for Correspondence
Jan Tack, MD, PhD, Department of Internal Medicine, Division of Gastroenterology, University Hospital Gasthuisberg, Herestraat 49, B-3000 Leuven, Belgium.
Tel: +32 16 34 42 25; fax: +32 16 34 44 19;


Background  Duodenal acid infusion induces gastric relaxation and sensitization to distension in healthy volunteers. The acid-sensitive mechanism is still unknown. We hypothesized that 5HT3-blockade can inhibit the acid-induced duodenogastric sensorimotor reflex in healthy volunteers.

Methods  Fourteen healthy volunteers were included in a randomized, double-blind placebo-controlled cross-over trial. An infusion tube with attached pH-electrode was positioned in the duodenum and a barostat balloon was located in the gastric fundus. Proximal gastric volume and sensitivity to distension were assessed before and during duodenal acid infusion and after pretreatment with intravenous (i.v.) ondansetron (a 5HT3-receptor antagonist, 8 mg) or saline. An overall perception score (0–6) and an assessment of nine dyspeptic symptoms by visual analogue scales (VAS) were obtained. Results are given as mean ± SEM.

Key Results  Ondansetron had no effect on duodenal pH and on the acid-induced increase of proximal gastric volume (increase of 80 ± 20 vs 83 ± 15 mL after ondansetron and placebo; effect of acid <0.001, between treatments ns). After ondansetron, the overall perception score during duodenal acidification and gastric distension was significantly decreased compared with placebo (= 0.01). There was no effect of ondansetron on the individual dyspeptic symptoms.

Conclusions & Inferences  Ondansetron decreased gastric sensitivity during duodenal acid infusion and gastric distension. 5HT3-receptors are involved in acid-induced duodenogastric sensitization, but not in the duodenogastric inhibitory motor reflex.