M E Levine1, J C Chillas, R M Stern, G W Knox. 1. Department of Psychology, The Pennsylvania State University, University Park 16802, USA. mel157@psu.edu
Abstract
BACKGROUND: The purpose of this study was to determine the effects of the serotonin (5-HT3) receptor-antagonist antiemetics ondansetron and granisetron on the development of gastric tachyarrhythmia, nausea, and other symptoms of motion sickness. METHODS: In a double-blind, counterbalanced, repeated measures design, 12 motion sickness susceptible college students participated in 3 sessions with an intersession interval of 1 wk. Participants received either 8 mg of ondansetron, 2 mg of granisetron, or placebo 1 h before exposure to a rotating optokinetic drum. Electrogastrograms (EGGs) were recorded during a 6-min baseline period and a subsequent 16-min drum rotation period. Subjective symptoms of motion sickness (SSMS) were obtained every 3 min during drum rotation. RESULTS: During drum rotation, gastric tachyarrhythmia increased significantly more during the placebo condition than during either of the serotonin (5-HT3) receptor antagonist conditions. However, maximum SSMS scores were not different among conditions. CONCLUSIONS: The serotonin (5-HT3) receptor antagonists inhibited the development of tachyarrhythmia, but did not prevent the development of nausea and other symptoms of motion sickness. The antiemetics ondansetron and granisetron may act as gastric anti-dysrhythmics, but their ability to arrest the development of gastric tachyarrhythmia was not sufficient for the prevention of nausea.
RCT Entities:
BACKGROUND: The purpose of this study was to determine the effects of the serotonin (5-HT3) receptor-antagonist antiemetics ondansetron and granisetron on the development of gastric tachyarrhythmia, nausea, and other symptoms of motion sickness. METHODS: In a double-blind, counterbalanced, repeated measures design, 12 motion sickness susceptible college students participated in 3 sessions with an intersession interval of 1 wk. Participants received either 8 mg of ondansetron, 2 mg of granisetron, or placebo 1 h before exposure to a rotating optokinetic drum. Electrogastrograms (EGGs) were recorded during a 6-min baseline period and a subsequent 16-min drum rotation period. Subjective symptoms of motion sickness (SSMS) were obtained every 3 min during drum rotation. RESULTS: During drum rotation, gastric tachyarrhythmia increased significantly more during the placebo condition than during either of the serotonin (5-HT3) receptor antagonist conditions. However, maximum SSMS scores were not different among conditions. CONCLUSIONS: The serotonin (5-HT3) receptor antagonists inhibited the development of tachyarrhythmia, but did not prevent the development of nausea and other symptoms of motion sickness. The antiemetics ondansetron and granisetron may act as gastric anti-dysrhythmics, but their ability to arrest the development of gastric tachyarrhythmia was not sufficient for the prevention of nausea.
Authors: Nathalie Percie du Sert; Kit M Chu; Man K Wai; John A Rudd; Paul Lr Andrews Journal: World J Gastroenterol Date: 2009-12-28 Impact factor: 5.742
Authors: D Bolognini; E M Rock; N L Cluny; M G Cascio; C L Limebeer; M Duncan; C G Stott; F A Javid; L A Parker; R G Pertwee Journal: Br J Pharmacol Date: 2013-03 Impact factor: 8.739