Water immersion increases urinary excretion of aquaporin-2 in healthy human

被引:17
作者
Buemi, M [1 ]
Corica, F [1 ]
Di Pasquale, G [1 ]
Aloisi, C [1 ]
Sofi, M [1 ]
Casuscelli, T [1 ]
Floccari, F [1 ]
Senatore, M [1 ]
Corsonello, A [1 ]
Frisina, N [1 ]
机构
[1] Univ Messina, Dept Internal Med, Chair Nephrol, I-98100 Messina, Italy
关键词
water immersion; atrial natriuretic factor; aquaporin-2; vasopressin;
D O I
10.1159/000045625
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Many previous studies have shown that aquaporin-2 (AQP2), the vasopressin-regulated water channel, is excreted in the urine and that the excretion increases in response to vasopressin. Moreover, recently a close correlation between AQP2 excretion in urine and kidney AQP2 expression has been demonstrated, showing that urinary excretion of AQP2 is a reliable indicator for AQP2 function. As head-out water immersion causes an expansion in the central vascular volume equal to that induced by 2 liters of saline, without modifying plasma composition, we used immersion in water to evaluate if the response to acute expansion of the central vascular volume could involve vasporessin (AVP) and AQP2. In healthy subjects, concentrations of plasma atrial natriuretic factor (ANF) and AVP, and urinary AQP2 were measured during a 2-hour immersion period. In all subjects, immersion caused a prompt and marked increase in immunoreactive ANF (23.0 +/- 2.12 pg/ml at second hour vs. 2.17 +/- 0.42 pg/ml at baseline) and in urinary excretion of AQP2 (23.9 +/- 2.69 pmol/mg creatinine at second hour vs. 4.42 +/- 0.14 pmol/mg creatinine at baseline), while a significant decrease was found in plasma AVP. Recovery was associated with a prompt return to pre-study levels. These findings demonstrate that heat-out water immersion stimulates urinary excretion of AQP2 in absence of an increase in plasma AVP. Copyright (C) 2000 S. Karger AG, Basel.
引用
收藏
页码:20 / 26
页数:7
相关论文
共 32 条
[1]   PHYSIOLOGICAL REGULATION OF ATRIAL-NATRIURETIC-PEPTIDE RECEPTORS IN RAT RENAL GLOMERULI [J].
BALLERMANN, BJ ;
HOOVER, RL ;
KARNOVSKY, MJ ;
BRENNER, BM .
JOURNAL OF CLINICAL INVESTIGATION, 1985, 76 (06) :2049-2056
[2]  
Baumgarten R, 1998, J AM SOC NEPHROL, V9, P1553
[3]   ATRIAL EXTRACTS INCREASE GLOMERULAR-FILTRATION RATE INVIVO [J].
BEASLEY, D ;
MALVIN, RL .
AMERICAN JOURNAL OF PHYSIOLOGY, 1985, 248 (01) :F24-F30
[4]   ATRIAL NATRIURETIC PEPTIDE AND URINARY PROSTAGLANDINS IN MAN [J].
BENZONI, D ;
GEOFFROY, J ;
WAEBER, B ;
BRUNNER, HR ;
BIOLLAZ, J ;
SASSARD, J .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1989, 28 (04) :397-402
[5]   MICROPUNCTURE STUDIES OF THE RENAL EFFECTS OF ATRIAL NATRIURETIC SUBSTANCE [J].
BRIGGS, JP ;
STEIPE, B ;
SCHUBERT, G ;
SCHNERMANN, J .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1982, 395 (04) :271-276
[6]   Cellular mechanisms of aquaporin trafficking [J].
Brown, D ;
Katsura, T ;
Gustafson, CE .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 1998, 275 (03) :F328-F331
[7]  
CODY RJ, 1985, HYPERTENSION, V7, P845
[8]  
Conte G, 1997, KIDNEY INT, pS28
[9]  
Deen PMT, 1998, CURR OPIN NEPHROL HY, V7, P37
[10]  
Elliot S, 1996, J AM SOC NEPHROL, V7, P403