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 in | American journal of physiology. Renal physiology Vol. 295; no. 5; pp. F1295 - F1300 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
United States
American Physiological Society
01.11.2008
|
Subjects | |
Online Access | Get full text |
ISSN | 1931-857X 1522-1466 |
DOI | 10.1152/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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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 ObjectType-Article-2 ObjectType-Feature-1 content type line 23 |
ISSN: | 1931-857X 1522-1466 |
DOI: | 10.1152/ajprenal.90407.2008 |