Voderholzer W A, Klauser A G, Mühldorfer B E, Fiedler F, Müller-Lissner S A
Medizinische Klinik, Klinikum Innenstadt, University of Munich.
Z Gastroenterol. 1995 Apr;33(4):189-92.
It was asked whether continuous infusion of arginine-vasopressin (AVP) could decrease stool output and gastrointestinal transit time in healthy volunteers.
Randomised single blind cross-over-design.
5 healthy male volunteers.
Continuous s.c. infusion of AVP (7.5 micrograms/d) for one week vs. 0.9% NaCl-solution (placebo). Some days before the experiment started, the volunteers underwent a two-day-thirsting-period (< 500 ml/day).
AVP-levels in serum, urine output, AVP-urine-excretion, stool frequency, stool weight, colonic transit time.
As compared to saline infusion both serum-levels of AVP and AVP-excretion in urine were about four times higher during AVP-infusion whereas they were doubled during thirsting. Accordingly urine output was lower when AVP-levels were high. Parameters of colonic motility did not differ significantly (stool frequency 6.8 +/- 0.8/week for placebo vs. 6.8 +/- 0.5/week during AVP, stool weight 200.3 +/- 25.0 g/d vs. 210.6 +/- 21.1 gld, total colonic transit 22.9 +/- 7.0 hours vs. 25.7 +/- 5.8 hours).
研究持续输注精氨酸加压素(AVP)是否能减少健康志愿者的粪便排出量并缩短胃肠道转运时间。
随机单盲交叉设计。
5名健康男性志愿者。
持续皮下输注AVP(7.5微克/天)一周,与0.9%氯化钠溶液(安慰剂)对照。在实验开始前几天,志愿者经历为期两天的限水期(每天<500毫升)。
血清中AVP水平、尿量、尿中AVP排泄量、排便频率、粪便重量、结肠转运时间。
与输注生理盐水相比,输注AVP期间血清AVP水平和尿中AVP排泄量均高出约四倍,而在限水期则翻倍。相应地,AVP水平高时尿量较低。结肠动力参数无显著差异(安慰剂组排便频率为6.8±0.8次/周,AVP组为6.8±0.5次/周;粪便重量安慰剂组为200.3±25.0克/天,AVP组为210.6±21.1克/天;结肠总转运时间安慰剂组为22.9±7.0小时,AVP组为25.7±5.8小时)。