EFFECTS OF EXPERIMENTAL POTASSIUM-DEPLETION ON RENAL-FUNCTION AND URINARY PROSTANOID EXCRETION IN NORMAL WOMEN DURING HYPOTONIC POLYURIA

被引:6
作者
AGNOLI, GC
BORGATTI, R
CACCIARI, M
GARUTTI, C
IKONOMU, E
LENZI, P
MARINELLI, M
机构
[1] Istituto di Clinica Medica II del, Università di Bologna
来源
CLINICAL PHYSIOLOGY | 1990年 / 10卷 / 04期
关键词
indomethacin; potassium depletion; prostanoids; renal function;
D O I
10.1111/j.1475-097X.1990.tb00796.x
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Summary. During hypotonic polyuria renal function studies by the clearance (cl.) method, and urinary PGE2, 6‐keto‐PGF1α and TxB2 determinations were performed on 14 healthy women in normal potassium balance (N) and 14 healthy women in sustained potassium depletion (KD) induced by low dietary potassium intake (≤ 10 mmol day‐1) and natriuretic treatment. By using different depletive patterns, two groups with estimated cumulative potassium deficits of 160 ± 43 mmol (KD1, n= 8) and 198 ± 22 mmol (KD2, n= 6), respectively, were obtained. (1) In both the KD1 and KD2 groups as compared to normal potassium balance (N), plasma potassium concentration and urinary potassium excretion were significantly lower; plasma renin activity was significantly higher. (2) Only in KD2 did significant changes appear in renal function and urinary prostanoid excretions. Besides a decrease in creatinine c1. and the urinary flow rate, an increase in fractional chloride excretion and a reduction in distal fractional chloride reabsorption were manifest. The plasma chloride concentration was reduced too. Urinary prostanoid excretions were significantly (6‐keto‐PGF1α, TxB2) or tendentially (PGE2) lower. (3) Indomethacin treatment resulted in changes in mean arterial pressure (increase) and creatinine cl. (decrease) which were not significantly different in normal potassium balance and KD groups. Only in KD2 did the drug significantly reduce the fractional salt and water excretions and the fractional sodium and chloride deliveries to the diluting segments. However, indomethacin was unable to correct the inhibition of distal fractional chloride reabsorption. Therefore, the potassium depletion attained in the KD2 group was efficacious in depressing renal prostanoid synthesis. This fact, in the presence of high levels of angiotensin II, induced a reduction of the glomerular filtration rate thus contributing to renal ability to retain chloride and potassium. Copyright © 1990, Wiley Blackwell. All rights reserved
引用
收藏
页码:345 / 362
页数:18
相关论文
共 39 条
[1]   EFFECTS OF CHRONIC POTASSIUM DEFICIENCY ON PLASMA RENIN ACTIVITY [J].
ABBRECHT, PH ;
VANDER, AJ .
JOURNAL OF CLINICAL INVESTIGATION, 1970, 49 (08) :1510-&
[2]  
ATTALLAH AA, 1981, J LAB CLIN MED, V97, P205
[3]   INFLUENCE OF POTASSIUM ADMINISTRATION AND OF POTASSIUM DEPRIVATION ON PLASMA RENIN IN NORMAL AND HYPERTENSIVE SUBJECTS [J].
BRUNNER, HR ;
BAER, L ;
SEALEY, JE ;
LEDINGHAM, JG ;
LARAGH, JH .
JOURNAL OF CLINICAL INVESTIGATION, 1970, 49 (11) :2128-+
[4]   EFFECTS OF 1 GRAM ORAL OR INTRAVENOUS ASPIRIN ON URINARY-EXCRETION OF THROMBOXANE-B2 AND 6-KETO-PGF1-ALPHA IN HEALTHY-SUBJECTS [J].
BUCCHI, F ;
BODZENTA, A ;
DEGAETANO, G ;
CERLETTI, C .
PROSTAGLANDINS, 1986, 32 (05) :691-701
[5]   RELATION BETWEEN POTASSIUM BALANCE AND ALDOSTERONE SECRETION IN NORMAL SUBJECTS AND IN PATIENTS WITH HYPERTENSIVE OR RENAL TUBULAR DISEASE [J].
CANNON, PJ ;
AMES, RP ;
LARAGH, JH .
JOURNAL OF CLINICAL INVESTIGATION, 1966, 45 (06) :865-&
[6]   RENAL EFFECTS OF DRUGS THAT INHIBIT PROSTAGLANDIN SYNTHESIS [J].
DUNN, MJ ;
ZAMBRASKI, EJ .
KIDNEY INTERNATIONAL, 1980, 18 (05) :609-622
[7]   EFFECTS OF MODERATE SHORT-TERM POTASSIUM-DEPLETION IN NORMAL HUMANS THE ROLE OF PROSTAGLANDINS [J].
DUSING, R ;
BARTTER, FC ;
GILL, JR ;
GULLNER, HG ;
LAKE, CR .
PROSTAGLANDINS & OTHER LIPID MEDIATORS, 1980, 20 (06) :971-979
[8]   ANALYSIS OF PROSTACYCLIN AND THROMBOXANE BIOSYNTHESIS IN CARDIOVASCULAR-DISEASE [J].
FITZGERALD, GA ;
PEDERSEN, AK ;
PATRONO, C .
CIRCULATION, 1983, 67 (06) :1174-1177
[9]   URINARY PROSTAGLANDINS - IDENTIFICATION AND ORIGIN [J].
FROLICH, JC ;
WILSON, TW ;
SWEETMAN, BJ ;
SMIGEL, M ;
NIES, AS ;
CARR, K ;
WATSON, JT ;
OATES, JA .
JOURNAL OF CLINICAL INVESTIGATION, 1975, 55 (04) :763-770
[10]  
GALVEZ OG, 1977, CIRC RES, V40, P11