Department of Pathophysiology, University of Leuven, Leuven, Belgium.
Aliment Pharmacol Ther. 2010 Jul;32(2):289-95. doi: 10.1111/j.1365-2036.2010.04351.x. Epub 2010 May 8.
Administration of 5-hydroxytryptamine (5HT) and selective 5HT receptor ligands modifies interdigestive motility in animals and in man.
To study the effect of citalopram, a selective 5-HT reuptake inhibitor, on interdigestive motility in man.
In 20 healthy subjects, antroduodenojejunal motor activity was studied manometrically. Basal interdigestive motor activity was recorded until the passage of two activity fronts. Ten minutes after the second activity front, placebo or 20 mg of citalopram was administered intravenously in a double-blind randomized fashion. Recording continued until the passage of two more activity fronts had occurred.
Administration of citalopram induced a premature small intestinal phase 3 after 35 +/- 6.4 min, compared to 120 +/- 17 min after placebo P < 0.01. Citalopram shortened MMC cycle length at the expense of phase 1 and phase 2 and significantly increased the motility index during phase 2 in the antrum and the small intestine.
In the interdigestive state in man, intravenous administration of the selective 5-HT reuptake inhibitor citalopram induces a premature intestinal phase 3 and suppresses gastric activity fronts. Phase 2 motility is stimulated both in the stomach and in the small bowel after citalopram. These data suggest that 5HT is involved in the control of interdigestive motility.
5-羟色胺(5HT)和选择性 5HT 受体配体的给药可改变动物和人体内的消化间期运动。
研究选择性 5HT 再摄取抑制剂西酞普兰对人类消化间期运动的影响。
在 20 名健康受试者中,通过测压法研究了十二指肠胃运动活动。在记录到两个活动波通过之前,记录基础消化间期运动活动。在第二个活动波通过后 10 分钟,以双盲随机方式静脉内给予安慰剂或 20mg 西酞普兰。记录继续进行,直到又通过了两个活动波。
与安慰剂后 120 +/- 17 分钟相比,西酞普兰给药后 35 +/- 6.4 分钟时诱导过早的小肠相 3,P < 0.01。西酞普兰缩短了 MMC 周期长度,牺牲了相 1 和相 2,并显著增加了胃和小肠相 2 期间的运动指数。
在人类消化间期状态下,静脉内给予选择性 5HT 再摄取抑制剂西酞普兰会导致过早的肠道相 3,并抑制胃活动波。西酞普兰后胃和小肠的相 2 运动均受到刺激。这些数据表明 5HT 参与了消化间期运动的控制。