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精氨酸加压素对健康志愿者粪便排出量及胃肠传输时间的影响。

The influence of arginine-vasopressin on stool output and gastrointestinal transit time in healthy volunteers.

作者信息

Voderholzer W A, Klauser A G, Mühldorfer B E, Fiedler F, Müller-Lissner S A

机构信息

Medizinische Klinik, Klinikum Innenstadt, University of Munich.

出版信息

Z Gastroenterol. 1995 Apr;33(4):189-92.

PMID:7793116
Abstract

OBJECTIVE

It was asked whether continuous infusion of arginine-vasopressin (AVP) could decrease stool output and gastrointestinal transit time in healthy volunteers.

DESIGN

Randomised single blind cross-over-design.

SUBJECTS

5 healthy male volunteers.

INTERVENTIONS

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).

MEASUREMENTS

AVP-levels in serum, urine output, AVP-urine-excretion, stool frequency, stool weight, colonic transit time.

RESULTS

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).

CONCLUSION

  1. AVP is well absorbed when applied subcutaneously. 2. AVP in the dosage given has no major influence on stool output and gastrointestinal transit time in healthy volunteers.
摘要

目的

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。

设计

随机单盲交叉设计。

受试者

5名健康男性志愿者。

干预措施

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)。

测量指标

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。

结果

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)。

结论

  1. 皮下应用时AVP吸收良好。2. 所给剂量的AVP对健康志愿者的粪便排出量和胃肠道转运时间无重大影响。

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