Effects of terlipressin on the aquaretic system: evidence of antidiuretic effects

The vasopressin analog terlipressin is believed to cause vasoconstriction selectively by V 1 receptor stimulation. However, a possible antidiuretic effect by V 2 receptor stimulation has never been ruled out. Twenty-two patients with ascites, including seven with refractory ascites, were included. T...

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Published inAmerican journal of physiology. Renal physiology Vol. 295; no. 5; pp. F1295 - F1300
Main Authors Krag, Aleksander, Bendtsen, Flemming, Pedersen, Erling Bjerregaard, Holstein-Rathlou, Niels-Henrik, Møller, Søren
Format Journal Article
LanguageEnglish
Published United States American Physiological Society 01.11.2008
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ISSN1931-857X
1522-1466
DOI10.1152/ajprenal.90407.2008

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Summary:The vasopressin analog terlipressin is believed to cause vasoconstriction selectively by V 1 receptor stimulation. However, a possible antidiuretic effect by V 2 receptor stimulation has never been ruled out. Twenty-two patients with ascites, including seven with refractory ascites, were included. The subjects were studied during a 400 ml/h oral water load before and after infusion of 2 mg of terlipressin (18 patients) or placebo infusion (4 patients). Effects on the V 2 receptors were assessed by evaluating aquaporin (AQP)2 excretion, free water clearance (C[Formula: see text]), urine osmolality (U osm ), and fractional distal water excretion (DFeH 2 O). After terlipressin the excretion of AQP2 increased by 89% [144 ng/mmol creatinine, 95% confidence interval (CI) 73–214 ng/mmol creatinine, P = 0.001]. C[Formula: see text] decreased 1.05 ml/min (from 0.17 to −0.89 ml/min, P = 0.001), and DFeH 2 O decreased 37% (19 vs. 12; 95% CI 2–11, P = 0.01). U osm increased by 27% (93 mosmol/kgH 2 O, 95% CI 23–164 mosmol/kgH 2 O, P = 0.02). Plasma sodium decreased 1.1 mmol/l ( P < 0.01). An increase in AQP2 excretion and a decrease in C[Formula: see text] and distal water excretion after terlipressin despite water loading is a clear indication of activation of the antidiuretic system (V 2 receptor effect).
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ISSN:1931-857X
1522-1466
DOI:10.1152/ajprenal.90407.2008