Effects of a 5-HT4 receptor agonist on oesophageal function and gastro-oesophageal reflux: studies using combined impedance-manometry and combined impedance-pH
Authors: TUTUIAN, R.1; MAINIE, I.1; ALLAN, R.2; HARGREAVES, K.2; AGRAWAL, A.1; FREEMAN, J.1; GALE, J.2; CASTELL, D. O.1
Source: Alimentary Pharmacology & Therapeutics, Volume 24, Number 1, July 2006 , pp. 155-162(8)
Publisher: Wiley-Blackwell
Abstract:
Summary Background 5-HT4 receptor agonists are used as promotility agents of the stomach, small and large intestine. There is limited information on the influence of 5-HT4 receptor agonists on oesophageal function and gastro-oesophageal reflux. Aim To evaluate the effects of tegaserod, a 5-HT4 agonist on oesophageal function using impedance-manometry and postprandial reflux using impedance-pH monitoring. Methods Twenty healthy volunteers were enrolled in a double-blind randomized three-period crossover placebo-controlled study. Impedance-manometry and impedance-pH monitoring after a refluxogenic meal were performed at baseline and after 2 days of dosing with tegaserod 6 mg b.d. or placebo. Multichannel intraluminal impedance-EM recorded pressure and bolus transit data during standardized swallows. Multichannel intraluminal impedance-pH monitoring recorded the number of 2-h postprandial acid and non-acid reflux episodes. Results We found no significant difference in distal oesophageal amplitude when subjects received placebo (median 94.5; range: 53-243 mmHg) or tegaserod (93.6; 43-216 mmHg). Bolus transit time was similar during dosing with placebo (7.1; 5.3-9.4 s) and tegaserod (7.2; 5.9-11.1 s). We observed similar numbers of acid and non-acid reflux episodes during dosing with placebo (5; 0-15 and 3; 0-18, respectively) and tegaserod (2; 0-11 and 4; 0-19, respectively). Conclusion Tegaserod, a 5-HT4 receptor agonist does not change oesophageal motility and gastro-oesophageal reflux parameters in healthy volunteers.Document Type: Research article
DOI: http://dx.doi.org/10.1111/j.1365-2036.2006.02968.x
Affiliations: 1: Division of Gastroenterology and Hepatology, Medical University of South Carolina, Charleston, SC, USA 2: Translational Medicine, Clinical R & D, Pfizer Global R&D, Sandwich, Kent, UK
Publication date: 2006-07-01
- In this: publication
- By this: publisher
- In this Subject: Pathology , Pharmacology , Surgery , Therapeutics & Alternative Medicine
- By this author: TUTUIAN, R. ; MAINIE, I. ; ALLAN, R. ; HARGREAVES, K. ; AGRAWAL, A. ; FREEMAN, J. ; GALE, J. ; CASTELL, D. O.

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