EFFECT OF CISAPRIDE ON MYOELECTRICAL AND MOTOR-RESPONSES OF ANTROPYLORODUODENAL REGION DURING INTRADUODENAL LIPID AND ANTRAL TACHYGASTRIA IN CONSCIOUS DOG
M. Edelbroek et al., EFFECT OF CISAPRIDE ON MYOELECTRICAL AND MOTOR-RESPONSES OF ANTROPYLORODUODENAL REGION DURING INTRADUODENAL LIPID AND ANTRAL TACHYGASTRIA IN CONSCIOUS DOG, Digestive diseases and sciences, 40(4), 1995, pp. 901-911
The myoelectrical and motor response of the antropyloroduodenal region
to intraduodenal nutrient stimulation or antral tachygastria represen
t useful models for, respectively, physiological and pathophysiologica
l gastric stasis to test the efficacy of prokinetic drugs. We evaluate
d the effects of an intravenous bolus of cisapride (0.63 mg/kg) on the
myoelectrical and motor response of the antropyloroduodenal region to
an intraduodenal triglyceride emulsion (10% Intralipid, 0.5 ml/min) o
r antral tachygastria in conscious dogs. Intraduodenal lipid suppresse
d antral motility (P < 0.05, compared to intraduodenal saline) and sti
mulated phasic pyloric contractions (P < 0.01, compared to intraduoden
al saline), a motor pattern known to be associated with delayed gastri
c emptying. During intraduodenal lipid stimulation cisapride virtually
abolished all isolated pyloric motor events (P < 0.05) and stimulated
antral and duodenal motility (P < 0.05 for both) and antropyloroduode
nal coordination (65% versus 15%; P < 0.05). Antral tachygastria was a
ssociated with a higher number of isolated pyloric motor events in the
fasted state [0.8 (0.7-1.1) per minute versus 0.2 (0-0.3) per minute;
P < 0.05], but not during intraduodenal lipid stimulation [1.1 (0.9-1
.7) per minute versus 1.2 (1.0-1.9) per minute; NS]. Cisapride decreas
ed the number and duration of spontaneous episodes of antral tachygast
ria during intraduodenal saline and lipid infusion (P < 0.05 for both)
and abolished the tachygastria-associated motor patterns. Cisapride i
nduced a 20% decrease in the antral slow-wave frequency during intradu
odenal saline and lipid, irrespective of gastric pacemaker rhythm. We
conclude that: (1) cisapride overcomes feedback from small intestinal
lipid receptors on myoelectrical and motor activities of the antropylo
roduodenal region and decreases antral slow-wave frequency, and (2) ci
sapride inhibits antral tachygastria and tachygastria-associated motor
patterns. These effects may contribute to the effective gastrokinetic
properties of cisapride in physiological and certain forms of pathoph
ysiological gastric stasis.