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Research Article Free access | 10.1172/JCI107410

Maximal Rates of Excretion and Synthesis of Urea in Normal and Cirrhotic Subjects

Daniel Rudman, Thomas J. DiFulco, John T. Galambos, Robert B. Smith III, Atef A. Salam, and W. Dean Warren

Department of Medicine, Emory University School of Medicine, and the Clinical Research Facility, Emory University Hospital, Atlanta, Georgia 30322

Department of Surgery, Emory University School of Medicine, and the Clinical Research Facility, Emory University Hospital, Atlanta, Georgia 30322

Find articles by Rudman, D. in: PubMed | Google Scholar

Department of Medicine, Emory University School of Medicine, and the Clinical Research Facility, Emory University Hospital, Atlanta, Georgia 30322

Department of Surgery, Emory University School of Medicine, and the Clinical Research Facility, Emory University Hospital, Atlanta, Georgia 30322

Find articles by DiFulco, T. in: PubMed | Google Scholar

Department of Medicine, Emory University School of Medicine, and the Clinical Research Facility, Emory University Hospital, Atlanta, Georgia 30322

Department of Surgery, Emory University School of Medicine, and the Clinical Research Facility, Emory University Hospital, Atlanta, Georgia 30322

Find articles by Galambos, J. in: PubMed | Google Scholar

Department of Medicine, Emory University School of Medicine, and the Clinical Research Facility, Emory University Hospital, Atlanta, Georgia 30322

Department of Surgery, Emory University School of Medicine, and the Clinical Research Facility, Emory University Hospital, Atlanta, Georgia 30322

Find articles by Smith, R. in: PubMed | Google Scholar

Department of Medicine, Emory University School of Medicine, and the Clinical Research Facility, Emory University Hospital, Atlanta, Georgia 30322

Department of Surgery, Emory University School of Medicine, and the Clinical Research Facility, Emory University Hospital, Atlanta, Georgia 30322

Find articles by Salam, A. in: PubMed | Google Scholar

Department of Medicine, Emory University School of Medicine, and the Clinical Research Facility, Emory University Hospital, Atlanta, Georgia 30322

Department of Surgery, Emory University School of Medicine, and the Clinical Research Facility, Emory University Hospital, Atlanta, Georgia 30322

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Published September 1, 1973 - More info

Published in Volume 52, Issue 9 on September 1, 1973
J Clin Invest. 1973;52(9):2241–2249. https://doi.org/10.1172/JCI107410.
© 1973 The American Society for Clinical Investigation
Published September 1, 1973 - Version history
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Abstract

When normal individuals eat 0.33 g protein N/kg body weight (BW)¾ per day, they excrete 10-15 mg urea N/h per kg BW¾. If they now ingest (at 0 h) 0.27 (dose A), 0.40 (dose B), 0.53 (dose C), 0.94 (dose D), or 1.33 (dose E) g protein N/kg BW¾ (in the form of casein, ovalbumin, or lactalbumin), the rate of urea N excretion accelerates within 4 h. At dose C a maximal rate of urinary urea N excretion (MRUE) is reached, which averages 55 mg urea N/h per kg BW¾ and which persists for 16 h. Higher doses of protein do not further accelerate urea excretion, but prolong the duration of MRUE to 28 h (after dose E). Blood urea N (BUN) rises by 7-20 mg/100 ml during the first 8 h after dose C to E, and remains stable within ±5 mg/100 ml during the ensuing 8-28 h of MRUE. Each increment of protein above dose C causes a further increment in plasma α-amino N. During infusion of free amino acids at a rate of 110 or 165 mg amino acid N/h per kg BW¾ for 12 h, rate of urea excretion increases to the MRUE value produced by dose C-E of oral protein.

These findings indicate that MRUE corresponds to a period of maximal rate of urea synthesis (MRUS). MRUS is greater than MRUE because one fraction of newly formed urea is hydrolyzed in the gastrointestinal tract, and another fraction may accumulate temporarily in body water during the MRUE period. Oral neomycin reduces the proportion of urea hydrolyzed in the gut to less than 20%; its extent is measured by recovery in the urine of a tracer dose of [14C]urea injected intramuscularly during determination of MRUE. Accumulation of urea in body water is estimated from increment in BUN during the period of MRUE measurement (8-24 h after dose E of casein) and from body water measured with 3H2O. Then MRUS is calculated as: ([mg urea N excreted between 8 and 24 h after dose E] + [BUN at 24 h − BUN at 8 h] × [body water]) × (100/% recovery [14C]urea) × (1/kg BW¾) × (1/16 h).

MRUS in 10 normal subjects averaged 65 mg urea N/h per kg BW¾ (range 55-76), and in 34 cirrhotics 27 mg urea N/h per kg BW¾ (range 6-64). Among 19 cirrhotic patients fed 40, 60, 80, or 100 g protein daily for successive 10 day periods, the occurrences of hyperammonemia, hyperaminoacidemia, and encephalopathy at each level of protein intake were inversely related to MRUS value.

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