Opposing effects of NaCl restriction and carbohydrate loading on urine volume in diabetic rats

被引:3
作者
O'Neill, H. A. [2 ]
Kwon, T-H. [3 ]
Ring, T. [4 ]
Dimke, H.
Lebeck, J.
Frokiaer, J. [5 ]
Collins, P. B. [2 ]
Nielsen, S.
Frische, S. [1 ]
机构
[1] Univ Aarhus, Inst Anat, Water & Salt Res Ctr, DK-8000 Aarhus C, Denmark
[2] RCSI, Dept Biochem, Dublin, Ireland
[3] Kyungpook Natl Univ, Sch Med, Dept Biochem & Cell Biol, Taegu 702701, South Korea
[4] Aalborg Hosp, Dept Nephrol, Aalborg, Denmark
[5] Aarhus Univ Hosp, Inst Clin Med, DK-8000 Aarhus N, Denmark
基金
新加坡国家研究基金会; 英国医学研究理事会;
关键词
carbohydrate intake; diabetes; diet; glomerular filtration rate; sodium restriction; GLUCAGON-LIKE PEPTIDE-1; SALT; HYPERFILTRATION; SODIUM; MELLITUS;
D O I
10.1111/j.1748-1716.2011.02260.x
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Aim: To test the effects of dietary NaCl and carbohydrate content on urine volume in diabetic rats. Methods: Streptozotocin-induced diabetic rats were subjected to NaCl restriction using either a NaCl-deficient carbohydrate-rich synthetic diet (Altromin C1036) supplemented to contain 0.16% NaCl (C1036 + lowNaCl) or a modified normal cereal-based diet (Altromin 1320) containing 0.086% NaCl (lowNaCl-1320). Normal diet contained 0.2683% NaCl. Results: Using the C1036 + lowNaCl diet, earlier reported paradoxical increases in water intake and urine volume of diabetic rats were reproduced. However, water intake and urine volume also increased in diabetic rats offered the synthetic C1036 diet supplemented with NaCl to normal levels. Using the lowNaCl-1320 diet, water intake and urine volume were markedly reduced. Highly significant correlations between urine volume and both osmotic output and urinary glucose excretion were found in diabetic rats on normal diet, but these correlations were absent in diabetic rats on synthetic diet, which showed higher urine volumes than expected from the correlations. In contrast, urine volume was significantly correlated with carbohydrate intake in diabetic rats, irrespective of the diet. Conclusions: (i) The synthetic diet dramatically increases the urine volume in STZ-DM rats irrespectively of NaCl content. (ii) Rats with STZ-DM on a normal diet show reduced water intake and urine volume in response to dietary NaCl restriction. (iii) A shift to high carbohydrate diet induces polyuria in STZ-DM rats. (iv) Urine volume in all STZ-DM rats only shows correlation with dietary carbohydrate intake. (v) Glucose-driven osmotic diuresis is unlikely to explain the carbohydrate-induced polyuria.
引用
收藏
页码:47 / 57
页数:11
相关论文
共 24 条
[1]   Salt restriction reduces hyperfiltration, renal enlargement, and albuminuria in experimental diabetes [J].
Allen, TJ ;
Waldron, MJ ;
Casley, D ;
Jerums, G ;
Cooper, ME .
DIABETES, 1997, 46 (01) :119-124
[2]  
[Anonymous], 2014, Biostatistical Analysis
[3]   Remodeling the cellular profile of collecting ducts by chronic carbonic anhydrase inhibition [J].
Bagnis, C ;
Marshansky, V ;
Breton, S ;
Brown, D .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2001, 280 (03) :F437-F448
[4]   SODIUM RESTRICTION CORRECTS HYPERFILTRATION OF DIABETES [J].
BANK, N ;
LAHORRA, MAG ;
AYNEDJIAN, HS ;
WILKES, BM .
AMERICAN JOURNAL OF PHYSIOLOGY, 1988, 254 (05) :F668-F676
[5]  
BIERI JG, 1977, J NUTR, V107, P1394
[6]   Regulation of Na+/H+ exchanger NHE3 by glucagon-like peptide 1 receptor agonist exendin-4 in renal proximal tubule cells [J].
Carraro-Lacroix, Luciene R. ;
Malnic, Gerhard ;
Girardi, Adriana C. C. .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2009, 297 (06) :F1647-F1655
[7]   Lack of A1 adenosine receptors augments diabetic hyperfiltration and glomerular injury [J].
Faulhaber-Walter, Robert ;
Chen, Limeng ;
Oppermann, Mona ;
Kim, Soo Mi ;
Huang, Yuning ;
Hiramatsu, Noriyuki ;
Mizel, Diane ;
Kajiyama, Hiroshi ;
Zerfas, Patricia ;
Briggs, Josephine P. ;
Kopp, Jeffrey B. ;
Schnermann, Jurgen .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2008, 19 (04) :722-730
[8]   Glucagon-like peptide 1 induces natriuresis in healthy subjects and in insulin-resistant obese men [J].
Gutzwiller, JP ;
Tschopp, S ;
Bock, A ;
Zehnder, CE ;
Huber, AR ;
Kreyenbuehl, M ;
Gutmann, H ;
Drewe, J ;
Henzen, C ;
Goeke, B ;
Beglinger, C .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2004, 89 (06) :3055-3061
[9]   The physiology of glucagon-like peptide 1 [J].
Holst, Jens Juul .
PHYSIOLOGICAL REVIEWS, 2007, 87 (04) :1409-1439
[10]   Gut-expressed gustducin and taste receptors regulate secretion of glucagon-like peptide-1 [J].
Jang, Hyeung-Jin ;
Kokrashvili, Zaza ;
Theodorakis, Michael J. ;
Carlson, Olga D. ;
Kim, Byung-Joon ;
Zhou, Jie ;
Kim, Hyeon Ho ;
Xu, Xiangru ;
Chan, Sic L. ;
Juhaszova, Magdalena ;
Bernier, Michel ;
Mosinger, Bedrich ;
Margolskee, Robert F. ;
Egan, Josephine M. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (38) :15069-15074