Evidence for a splanchnic sodium input monitor regulating renal sodium excretion in man. Lack of dependence upon aldosterone.
Open accessAbstract
Eight normal male subjects were placed on a constant 10 mEq sodium, 60 mEq potassium diet for 5 days. At 8:00 a.m. on the 5th day, the subjects were given a standard dose of 100 mEq of sodium orally or intravenously. Subjects receiving oral sodium also received 200ml of 5% dextrose in water intravenously, and those receiving intravenous sodium also received placebo capsules orally. Water intake and posture were controlled. The subjects then returned to a free diet for 1 month and subsequently were restudied by using the opposite route of sodium administration. The subjects given the oral sodium load excreted greater quantities of sodium in their urine than those repleted intravenously. The differential natriuresis was significant as early as 2 hours after sodium loading. Plasma aldosterone concentration was similar irrespective of the route of sodium administration. Six patients with primary adrenocortical insufficiency and documented hypoaldosteronism were studied with the same protocol after 5 days of 50 mEq sodium, 60 mEq potassium intake. They also had significantly greater natriuresis after oral than intravenous sodium administration. The data suggest the presence of a splanchnic input monitor for sodium which partially regulates renal sodium excretion and is not dependent upon a turn-off mechanism for aldosterone secretion.
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In a sodium-depleted state, an oral sodium load is more rapidly excreted by the kidneys than an intravenous sodium load.
“The proposals were based on studies in humans showing that in a sodium-depleted state, an oral sodium load is more rapidly excreted by the kidneys than an intravenous sodium load (24).”
From GLP-1 agonists in the treatment of chronic kidney disease in type 2 diabetes and obesity (2025) · cites this paper as [24]
Cites
SIMPSON, S. A., Tait, J. F., Wettstein, A., Neher, R., Euw, J. V., & Reichstein, T. (1953) · Cellular and Molecular Life Sciences · doi:10.1007/bf02155834 · Cited by 283 · see citing works
Diurnal Variation of Plasma Aldosterone, Cortisol and Renin Activity in Supine Man
Katz, F. H., Romfh, P., SMITH, J. A., Roper, E., Barnes, J. S., & BOYD, J. B. (1975) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem-40-1-125 · Cited by 208 · see citing works
Luetscher, J. A., & Johnson, B. B. (1954) · Journal of Clinical Investigation · doi:10.1172/jci103022 · Cited by 205 · see citing works
Lennane, R. J., Peart, W. S., Carey, R. M., & Shaw, J. (1975) · Clinical Science · doi:10.1042/cs0490433 · Cited by 120 · see citing works
Self-citationJj, D., Roe, J. W., & Horrocks, P. M. (1967) · PubMed · Cited by 70 · see citing works
EFFECTS OF GLUCAGON ON RENAL FUNCTION IN MAN*
Elrick, H., Huffman, E. R., HLAD, C. J., WIIIPPLE, N., Staub, A., Smith, A. E., & YEARWOOD-DRAYTON, V. (1958) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem-18-8-813 · Cited by 69 · see citing works
Effect of Chronic Bile Duct Obstruction on Renal Handling of Salt and Water
Better, O. S., & Massry, S. G. (1972) · Journal of Clinical Investigation · doi:10.1172/jci106826 · Cited by 63 · see citing works
Hepatic receptors in control of sodium excretion in anesthetized cats
Passo, S. S., Thornborough, & Rothballer, A. B. (1973) · American Journal of Physiology-Legacy Content · doi:10.1152/ajplegacy.1973.224.2.373 · Cited by 60 · see citing works
Espiner, E. A., Tucci, J. R., Jagger, P. I., & Lauler, D. P. (1967) · New England Journal of Medicine · doi:10.1056/nejm196707062770101 · Cited by 48 · see citing works
Gastrointestinal control of sodium excretion in sodium-depleted conscious rabbits
Carey, R. M., Smith, & Ortt, E. M. (1976) · American Journal of Physiology-Legacy Content · doi:10.1152/ajplegacy.1976.230.6.1504 · Cited by 42 · see citing works
Self-citationWhat mediates the renal vascular response to a salt load in normal man?
Hollenberg, N. K., Adams, D. F., Solomon, H., Abrams, H. L., & Merrill, J. P. (1972) · Journal of Applied Physiology · doi:10.1152/jappl.1972.33.4.491 · Cited by 17 · see citing works
Beckerhoff, R., Kappeler, M., Vetter, W., Armbruster, H., & Siegenthaler, W. E. (1975) · Clinical Science · doi:10.1042/cs0480413 · Cited by 2 · see citing works
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Muskiet, M. H. A., Tonneijck, L., Smits, M. M., van Baar, M. J. B., Kramer, M. H. H., Hoorn, E. J., Joles, J. A., & van Raalte, D. H. (2017) · Nature Reviews Nephrology · doi:10.1038/nrneph.2017.123 · Cited by 407 · see citing works
Long-term space flight simulation reveals infradian rhythmicity in human Na(+) balance
Rakova, N., Jüttner, K., Dahlmann, A., Schröder, A., Linz, P., Kopp, C., Rauh, M., Goller, U., Beck, L., Agureev, A., et al. (2013) · Cell Metabolism · doi:10.1016/j.cmet.2012.11.013 · Cited by 328 · see citing works
The gut–renal axis: do incretin-based agents confer renoprotection in diabetes?
Muskiet, M. H. A., Smits, M. M., Morsink, L. M., & Diamant, M. (2013) · Nature Reviews Nephrology · doi:10.1038/nrneph.2013.272 · Cited by 182 · see citing works
Uroguanylin and guanylin peptides: pharmacology and experimental therapeutics
FORTEJR, L. (2004) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2004.08.007 · Cited by 155 · see citing works
Long-term sodium balance in humans in a terrestrial space station simulation study
Titze, J. M., Maillet, A., Lang, R., Gunga, H. C., Johannes, B. W., Gauquelin‐Koch, G., Kihm, E., Larina, I., Gharib, C., & Kirsch, K. A. (2002) · American Journal of Kidney Diseases · doi:10.1053/ajkd.2002.34908 · Cited by 150 · see citing works
Abnormal renal sodium handling in essential hypertension
Hollenberg, N. K., Moore, T. J., Shoback, D., Redgrave, J., Rabinowe, S. L., & Williams, G. H. (1986) · The American Journal of Medicine · doi:10.1016/0002-9343(86)90291-3 · Cited by 132 · see citing works
Fonteles, M. C., Greenberg, R. N., Monteiro, H. S. A., Currie, M. G., & Forte, L. R. (1998) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.1998.275.2.f191 · Cited by 117 · see citing works
Guanylin and uroguanylin induce natriuresis in mice lacking guanylyl cyclase-C receptor
Carrithers, S. L., Ott, C. E., Hill, M. J., Johnson, B. R., Cai, W., Chang, J. J., Shah, R. G., Sun, C., Mann, E. A., Fonteles, M. C., et al. (2003) · Kidney International · doi:10.1111/j.1523-1755.2004.00375.x · Cited by 95 · see citing works
Michell, A. R., Debnam, E. S., & Unwin, R. J. (2007) · Annual Review of Physiology · doi:10.1146/annurev.physiol.69.040705.141330 · Cited by 95 · see citing works
Salt and water homeostasis: uroguanylin is a circulating peptide hormone with natriuretic activity
Forte, L. R., Fan, X., & Hamra, F. K. (1996) · American Journal of Kidney Diseases · doi:10.1016/s0272-6386(96)90318-2 · Cited by 79 · see citing works
Natriuretic Hormones in Brain Function
Hodes, A., & Lichtstein, D. (2014) · Frontiers in Endocrinology · doi:10.3389/fendo.2014.00201 · Cited by 76 · see citing works
Guanylin peptides: renal actions mediated by cyclic GMP
Forte, L. R., London, R. M., Freeman, R. H., & Krause, W. J. (2000) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.2000.278.2.f180 · Cited by 71 · see citing works
A Novel Guanylin Family (Guanylin, Uroguanylin, and Renoguanylin) in Eels
Yuge, S., Inoue, K., Hyodo, S., & Takei, Y. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m303111200 · Cited by 69 · see citing works
Fan, X., Wang, Y., London, R. M., Eber, S. L., Krause, W. J., Freeman, R. H., & Forte, L. R. (1997) · Endocrinology · doi:10.1210/en.138.11.4636 · Cited by 64 · see citing works
Gastrin and D 1 Dopamine Receptor Interact to Induce Natriuresis and Diuresis
Chen, Y., Asico, L. D., Zheng, S., Villar, V. A. M., He, D., Zhou, L., Zeng, C., & José, P. A. (2013) · Hypertension · doi:10.1161/hypertensionaha.113.01094 · Cited by 61 · see citing works
Nephroprotective effects of GLP-1 receptor agonists: where do we stand?
Mosterd, C. M., Bjornstad, P., & van Raalte, D. H. (2020) · Journal of Nephrology · doi:10.1007/s40620-020-00738-9 · Cited by 56 · see citing works
Cardiac and intestinal natriuretic peptides: Insights from genetically modified mice
Kühn, M. (2005) · Peptides · doi:10.1016/j.peptides.2004.08.031 · Cited by 57 · see citing works
Mechanisms of Guanylin Action Via Cyclic GMP in the Kidney
Forte, L. R., London, R. M., Krause, W. J., & Freeman, R. H. (2000) · Annual Review of Physiology · doi:10.1146/annurev.physiol.62.1.673 · Cited by 56 · see citing works
The kidney and cardiovascular outcome trials
Bloomgarden, Z. T. (2017) · Journal of Diabetes · doi:10.1111/1753-0407.12616 · Cited by 51 · see citing works
Sodium homeostasis: Steady states without a set point
Bonventre, J. V., & Leaf, A. (1982) · Kidney International · doi:10.1038/ki.1982.113 · Cited by 45 · see citing works
Moss, N., Fellner, R. C., Qian, X., Yu, S. J., Li, Z., Nakazato, M., & Goy, M. F. (2008) · Endocrinology · doi:10.1210/en.2007-1725 · Cited by 45 · see citing works
Splanchnic control of vasopressin secretion in conscious rats
Choi‐Kwon, S., McCarty, R. C., & Baertschi, A. J. (1990) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1990.259.1.e19 · Cited by 45 · see citing works
Changes in Urinary Levels and Renal Expression of Uroguanylin on Low or High Salt Diets in Rats
Fukae, H., Kinoshita, H., Fujimoto, S., Kita, T., Nakazato, M., & Eto, T. (2002) · The Nephron journals/Nephron journals · doi:10.1159/000063311 · Cited by 44 · see citing works
Phenomenological analysis of renal regulation of sodium and potassium balance
Walser, M. (1985) · Kidney International · doi:10.1038/ki.1985.89 · Cited by 42 · see citing works
Qian, X., Moss, N., Fellner, R. C., & Goy, M. F. (2008) · Endocrinology · doi:10.1210/en.2007-1724 · Cited by 40 · see citing works
Gastrointestinal osmoreceptors and renal sodium excretion in humans
Andersen, L. J., Jensen, T. U. S., Bestle, M. H., & Bie, P. (2000) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.2000.278.2.r287 · Cited by 39 · see citing works
Kumar, R. (2009) · Current Opinion in Nephrology & Hypertension · doi:10.1097/mnh.0b013e32832b5094 · Cited by 37 · see citing works
Dubois, S. K., Kishimoto, I., Lillis, T. O., & Garbers, D. L. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.8.4369 · Cited by 37 · see citing works
Lessa, L. M. A., Carraro‐Lacroix, L. R., Crajoinas, R. O., Bezerra, C. N. A., Dariolli, R., Girardi, A. C. C., Fonteles, M. C., & Malnic, G. (2012) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00385.2011 · Cited by 35 · see citing works
Liu, T., & José, P. A. (2012) · Endocrinology · doi:10.1210/en.2012-1813 · Cited by 34 · see citing works
Gastrointestinal–Renal Axis: Role in the Regulation of Blood Pressure
Yang, J., José, P. A., & Zeng, C. (2017) · Journal of the American Heart Association · doi:10.1161/jaha.117.005536 · Cited by 32 · see citing works
Jiang, X., Chen, W., Liu, X., Wang, Z., Liu, Y., Felder, R. A., Gildea, J. J., José, P. A., Qin, C., & Yang, Z. (2016) · PLoS ONE · doi:10.1371/journal.pone.0146641 · Cited by 30 · see citing works
The importance of the gastrorenal axis in the control of body sodium homeostasis
José, P. A., Yang, Z., Zeng, C., & Felder, R. A. (2016) · Experimental Physiology · doi:10.1113/ep085286 · Cited by 28 · see citing works
Preston, R. A., Afshartous, D. R., Forte, L. R., Rodco, R., Alonso, A. B., Garg, D. C., & Raij, L. R. (2012) · Kidney International · doi:10.1038/ki.2012.269 · Cited by 26 · see citing works
Epstein, M., & Lifschitz, M. D. (2016) · Kidney International Reports · doi:10.1016/j.ekir.2016.03.001 · Cited by 25 · see citing works
GLP-1 agonists in the treatment of chronic kidney disease in type 2 diabetes and obesity
Cooper, M. E., & van Raalte, D. H. (2025) · Journal of Clinical Investigation · doi:10.1172/jci194749 · Cited by 24 · see citing works
“The proposals were based on studies in humans showing that in a sodium-depleted state, an oral sodium load is more rapidly excreted by the kidneys than an intravenous sodium load (24).”
Factors influencing renal sodium reabsorption in volume expansion
Knox, F. G., & Haas, J. A. (1982) · Reviews of physiology, biochemistry and pharmacology · doi:10.1007/bfb0030503 · Cited by 24 · see citing works
Mu, J. Y., Hansson, G. C., Bergström, G. M. L., & Lundgren, O. (1995) · Acta Physiologica Scandinavica · doi:10.1111/j.1748-1716.1995.tb09848.x · Cited by 22 · see citing works
Santos‐Neto, M. S., Carvalho, A. F., Monteiro, H. S. A., Forte, L. R., & Fonteles, M. C. (2006) · Regulatory Peptides · doi:10.1016/j.regpep.2006.04.017 · Cited by 21 · see citing works
Millet, D., DESGRANGES, C., Campan, M., Gadeau, A., & Costerousse, O. (1992) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1992.tb16936.x · Cited by 21 · see citing works
Modification of renal and tissue cation transport by cholecystokinin octapeptide in the rabbit.
Duggan, K. A., Hams, G., & Macdonald, G. J. (1988) · The Journal of Physiology · doi:10.1113/jphysiol.1988.sp017017 · Cited by 16 · see citing works
Sodium depletion decreases hepatic metabolism of vasoactive intestinal peptide in the rabbit.
Duggan, K. A., Hawley, C. M., Macdonald, G. J., & Shelley, S. (1989) · The Journal of Physiology · doi:10.1113/jphysiol.1989.sp017838 · Cited by 16 · see citing works
Effects of Uroguanylin, an Intestinal Natriuretic Peptide, on Tubuloglomerular Feedback
Tao, W. A. N. G., Kawabata, M., Haneda, M., & TAKABATAKE, T. (2003) · Hypertension Research · doi:10.1291/hypres.26.577 · Cited by 15 · see citing works
The use of glycaemic index tables to predict glycaemic index of breakfast meals
Brand-Miller, J. C., & Wolever, T. M. S. (2005) · British Journal Of Nutrition · doi:10.1079/bjn20041423 · Cited by 15 · see citing works
Brain-gut peptides, renal function and cell growth
Unwin, R. J., Ganz, M. D., & Sterzel, R. B. (1990) · Kidney International · doi:10.1038/ki.1990.83 · Cited by 15 · see citing works
José, P. A., Felder, R. A., Yang, Z., Zeng, C., & Eisner, G. M. (2016) · Hypertension · doi:10.1161/hypertensionaha.115.06424 · Cited by 14 · see citing works
Control of Renal Solute Excretion by Enteric Signals and Mediators
Thomas, L. F., & Kumar, R. (2008) · Journal of the American Society of Nephrology · doi:10.1681/asn.2007101122 · Cited by 14 · see citing works
Fellner, R. C., Moss, N., & Goy, M. F. (2016) · Physiological Reports · doi:10.14814/phy2.12782 · Cited by 14 · see citing works
Guanylin peptides: cyclic GMP signaling mechanisms
Forte, L. R., Freeman, R. H., Krause, W. J., & London, R. M. (1999) · Brazilian Journal of Medical and Biological Research · doi:10.1590/s0100-879x1999001100002 · Cited by 14 · see citing works
Impaired renal response to splanchnic infusion of hypertonic saline in conscious cirrhotic rats
López-Novoa, J. M., & Martinez-Maldonado, M. (1982) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.1982.242.4.f390 · Cited by 13 · see citing works
Pendrin, a Novel Transcriptional Target of the Uroguanylin System
Rozenfeld, J., Tal, O., Kladnitsky, O., Adler, L., Efrati, E., Carrithers, S. L., Alper, S. L., & Zelikovic, I. (2013) · Cellular Physiology and Biochemistry · doi:10.1159/000356641 · Cited by 12 · see citing works
Dietary phosphate-dependent growth is not mediated by changes in plasma phosphate concentration.
Landsman, A., Lichtstein, D., Bacaner, M. B., & Ilani, A. (2001) · PubMed · Cited by 12 · see citing works
Is there an intestinal natriuretic factor?*
Lundgren, O., & Hansson, G. C. (1991) · Acta Physiologica Scandinavica · doi:10.1111/j.1748-1716.1991.tb09039.x · Cited by 12 · see citing works
Guanylin peptide family: history, interactions with ANP, and new pharmacological perspectives
Fonteles, M. C., & do Nascimento, N. R. F. (2011) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/y11-050 · Cited by 11 · see citing works
The guanylin peptide family and the proposed gastrointestinal–renal natriuretic signaling axis
Mueller, T., & Dieplinger, B. (2012) · Kidney International · doi:10.1038/ki.2012.344 · Cited by 11 · see citing works
Santos‐Neto, M. S., Carrithers, S. L., Carvalho, A. F., Monteiro, H. S. A., Greenberg, R. N., Forte, L. R., & Fonteles, M. C. (2003) · Pharmacology & Toxicology · doi:10.1034/j.1600-0773.2003.920302.x · Cited by 9 · see citing works
Sodium intake for athletes before, during and after exercise: review and recommendations
McCubbin, A. J. (2025) · Performance Nutrition · doi:10.1186/s44410-025-00011-9 · Cited by 11 · see citing works
Bridges, E., Altherwi, T. I., Correa, J. A., & Hew‐Butler, T. (2018) · Clinical Journal of Sport Medicine · doi:10.1097/jsm.0000000000000573 · Cited by 8 · see citing works
The Small Intestine, Salt Intake and Arterial Hypertension
Mu, J. Y., Hansson, G. C., & Lundgren, O. (1995) · Blood Pressure · doi:10.3109/08037059509077573 · Cited by 8 · see citing works
Kipnowski, J., Düsing, R., & Kramer, H. (1981) · Journal of Molecular Medicine · doi:10.1007/bf01695895 · Cited by 8 · see citing works
The rapid adjustment of renal sodium excretion to changes in dietary sodium intake in sheep
Grim, C. E., & Scoggins, B. A. (1986) · Life Sciences · doi:10.1016/0024-3205(86)90533-3 · Cited by 7 · see citing works
Hansson, G. C., Mu, J. Y., & Lundgren, O. (1995) · Blood Pressure · doi:10.3109/08037059509077580 · Cited by 6 · see citing works
Titze, J. M., Ларина, И. М., Garib, K., Kirsch, K. O., Maye, A., Lang, R., Gunga, H., Johanes, B., Gochlen-Koch, H., & Kim, E. (2003) · Human Physiology · doi:10.1023/a:1025820118198 · Cited by 5 · see citing works
Impaired renal response to portal infusion of hypertonic saline in adriamycin‐treated rats
Jirakulsomchok, D., Napawachirahat, S., Kunbootsri, N., Suttitum, T., Wannanon, P., Wyss, J. M., & Roysommuti, S. (2012) · Clinical and Experimental Pharmacology and Physiology · doi:10.1111/j.1440-1681.2012.05722.x · Cited by 4 · see citing works
Slotki, I. N., & Skorecki, K. L. (2012) · Elsevier eBooks · doi:10.1016/b978-1-4160-6193-9.10014-4 · Cited by 3 · see citing works
Osmotic and Ionic Regulation in Mammals
Kinne, R. K. H., & Zeidel, M. L. (2008) · CRC Press eBooks · doi:10.1201/9780849380525.ch12 · Cited by 3 · see citing works
Unwin, R. J. (1989) · Steinkopff eBooks · doi:10.1007/978-3-642-72417-6_2 · Cited by 3 · see citing works
The Interaction of Kidneys and Gut in Development of Salt-Sensitive Hypertension
Chrysant, S. G. (2023) · Cardiology in Review · doi:10.1097/crd.0000000000000518 · Cited by 3 · see citing works
Extracellular Fluid Volume Homeostasis
Poole, B. D., Abraham, W. T., & Schrier, R. W. (2005) · doi:10.1002/9780470987476.ch1 · Cited by 2 · see citing works
Forte, L. R., & Fonteles, M. C. (2008) · Elsevier eBooks · doi:10.1016/b978-012088488-9.50022-x · Cited by 1 · see citing works
Fellner, R. C. (2019) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/3ts9-0f77
Alifieris, C. E., Trafalis, D. T., Efstratopoulos, A. D., & Alifieris, E. K. (2017) · Autonomic Neuroscience · doi:10.1016/j.autneu.2017.05.005
Neto, V. L. M., Araújo, I. C. D., Rôla, T. B. M., Magalhães, P. J. C., Rodrigues, F. A. P., Lima, A. A. M., & Santos, A. A. (2026) · Brazilian Journal of Medical and Biological Research · doi:10.1590/1414-431x2025e15041
Guanylin peptides in heart failure
Narayan, H. (2013) · Figshare
- Authors
- Carey, R. M.
- Corresponding author
- Carey, R M
- ORCID
- Carey, R M
- Venue
- Circulation Research
- Published
- 1978-07
- Volume
- 43
- Issue
- 1
- Pages
- 19-23
- ISSN
- 0009-7330 (ISSN-L)
- 1524-4571
- OpenAlex
- W1986644847
- Cited by
- 76
- References
- 12
- Citations by year
- 2026: 1 · 2025: 2 · 2023: 1 · 2020: 1 · 2019: 1 · 2018: 1 · 2017: 4 · 2016: 5 · 2014: 1 · 2013: 5 · 2012: 6
- FWCI
- 0.42
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Circulation Research (publishedVersion)
- PubMed (publishedVersion)
- Funders
- American Heart Association
- National Institutes of Health
- Topics
- Health Sciences › Nursing › Nutrition and Dietetics › Sodium Intake and Health
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Renin-Angiotensin System Studies
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Hormonal Regulation and Hypertension
- Keywords
- renal sodium excretion, sodium excretion, aldosterone, hypoaldosteronism, Addison's disease, sodium intake, plasma aldosterone
- MeSH terms
- Administration, Oral, Adult, Aldosterone, Humans, Injections, Intravenous, Kidney, Male, Potassium, Sodium, Spleen
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