Key result
Intravenous administration of selective beta-adrenergic agonists (terbutaline and prenalterol) did not significantly alter sigmoid motility stimulated by cholecystokinin compared with placebo.
Why the study?
Do selective beta-adrenergic agonists (terbutaline or prenalterol) inhibit cholecystokinin-stimulated sigmoid motility in healthy subjects?
RCT (n=12)
double-blind
randomized
Do selective beta-adrenergic agonists (terbutaline or prenalterol) inhibit cholecystokinin-stimulated sigmoid motility in healthy subjects?
Selective beta-1 and beta-2 adrenergic agonists do not inhibit colonic motility when stimulated by cholecystokinin in healthy humans.
Does not inhibit CCK-stimulated sigmoid motility; challenges beta-adrenergic modulation hypotheses and directs research to alternative pathways.
Sigmoid motility, stimulated by the octapeptide of cholecystokinin (OP-CCK) and the effects of beta-adrenoceptor agonists, was studied in 12 healthy subjects in a randomized, double-blind fashion. Sigmoid pressure was recorded 18-20 cm from the anus, and contractile activity quantified as the area under pressure waves for three 25-min periods. OP-CCK (sincalide), 80 ng X kg-1 X h-1, was continuously infused throughout each session, resulting in a high sigmoid motility index. Preceded by a control period, terbutaline (beta-2 agonist), prenalterol (beta-1 agonist), or placebo was injected on 3 separate days. After 1 mg + 4 mg prenalterol or 0.25 mg + 0.25 mg terbutaline intravenously no significant changes in motility pattern were seen compared with the control period. Terbutaline and prenalterol infusions were followed by a dose-dependent increase of systolic blood pressure and heart rate. After placebo no effect on blood pressure or heart rate was seen. The study shows that CCK significantly enhances sigmoid motility in man and that selective beta-adrenergic agonists do not show any inhibitory influence on colonic motility stimulated with CCK. Since terbutaline inhibits sigmoid and rectal motility in man during rectal distention, it is suggested that the inhibitory effect of beta-2-adrenoceptor agonists may be dependent on the mode of background stimulation of the colon.
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Lyrenäs et al. (1985) conducted an RCT in healthy subjects (n=12). Terbutaline or prenalterol vs. Placebo was evaluated on Sigmoid motility pattern (contractile activity quantified as area under pressure waves). Intravenous administration of selective beta-adrenergic agonists (terbutaline and prenalterol) did not significantly alter sigmoid motility stimulated by cholecystokinin compared with placebo.
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