Cited by 76Sodium Intake and HealthRenin-Angiotensin System StudiesHormonal Regulation and Hypertension

Evidence for a splanchnic sodium input monitor regulating renal sodium excretion in man. Lack of dependence upon aldosterone.

Open access
Carey, R M·1978·Circulation Research

Abstract

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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Crossref · 10.1161/01.res.43.1.19

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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).”

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Authors
Carey, R. M.
Corresponding author
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
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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