Lyrenäs E, Abrahamsson H, Dotevall G
Scand J Gastroenterol. 1985 Dec;20(10):1169-74. doi: 10.3109/00365528509089271.
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.
以随机、双盲方式,对12名健康受试者研究了胆囊收缩素八肽(OP-CCK)刺激下的乙状结肠运动及β-肾上腺素能受体激动剂的作用。在距肛门18 - 20厘米处记录乙状结肠压力,收缩活动量化为三个25分钟时段压力波下的面积。每次实验全程持续输注80 ng·kg⁻¹·h⁻¹的OP-CCK(辛卡利特),导致乙状结肠运动指数较高。在对照期之后,在3个不同日期分别注射特布他林(β-2激动剂)、普瑞特罗(β-1激动剂)或安慰剂。静脉注射1毫克 + 4毫克普瑞特罗或0.25毫克 + 0.25毫克特布他林后,与对照期相比,运动模式未见明显变化。输注特布他林和普瑞特罗后,收缩压和心率呈剂量依赖性升高。注射安慰剂后,血压和心率未见影响。该研究表明,CCK可显著增强人体乙状结肠运动,选择性β-肾上腺素能激动剂对CCK刺激的结肠运动未显示任何抑制作用。由于特布他林在直肠扩张时可抑制人体乙状结肠和直肠运动,提示β-2肾上腺素能受体激动剂的抑制作用可能取决于结肠背景刺激的方式。