Little information is available on the hemodynamic response (renal reserve) of the diabetic kidney during an acute amino acid infusion, which has been shown to increase glomerular filtration rate (GFR) in normal humans. We recently found that the infusion of ketone bodies is able to raise GFR in both normal subjects and insulin-dependent diabetes mellitus (IDDM) patients. The aim of this study was to evaluate the renal reserve in 15 IDDM patients with a duration of diabetes of >9 yr [8 with albumin excretion rate <15 μg/min (group 1) and 7 with albumin excretion rate >100 μg/min (group 2)] and in 8 normal subjects during amino acid infusion (33 μmol · kg−1 · min−1 , Travasol 10% wt/vol solution containing 0.154 mM sodium chloride concentration; Travenol, Savage, MD) and during acetoacetic sodium salt (25 μmol · kg−1 · min−1) infusion. Blood glucose was clamped at euglycemic levels. The infusion of sodium acetoacetate resulted in a 10- to 15-fold increase in circulating concentrations of ketone bodies, which were similar in magnitude in normal subjects and diabetic patients. The GFR peak increase above baseline after sodium acetoacetate infusion was 28% in normal subjects and 27% in group 1 and 19% in group 2 diabetic patients. The infusion of amino acid solution produced a three- to fivefold increase in plasma concentrations of amino acids in both normal subjects and diabetic patients. The GFR peak increase above baseline after amino acid infusion was significantly lower in diabetic patients (IDDM group 1: 5%, P < .01; IDDM group 2: 6%, P < .01) than in normal subjects (38%). During sodium acetoacetate infusion, proximal sodium reabsorption increased as well as distal sodium delivery in normal subjects and group 1 and group 2 IDDM patients. During amino acid infusion, only normal subjects showed a significant increase in proximal sodium reabsorption and distal sodium delivery, whereas no change was found in group 1 and group 2 IDDM patients. Amino acid infusion resulted in a marked increase in the albumin fractional clearance rate in both normal subjects and diabetic patients. On the contrary, ketone body infusion slightly increased the albumin fractional clearance rate in group 2 diabetic patients but not in group 1 diabetic patients and normal subjects. This study demonstrates that long-standing diabetic patients, irrespective of the presence of impaired renal function, show a peculiar defect in the kidney hemodynamic response to amino acid but not to ketone body infusion. These results question the use of an amino acid load to test for glomerular filtration reserve in diabetic patients, because a lack of response may simply be related to an altered response of the kidney to amino acids. A macula densa feedback mechanism could not account for the increase in GFR after both amino acid and ketone body infusion, because these compounds increase the sodium distal delivery. Amino acids increase albumin excretion rate with a mechanism independent of GFR and renal plasma flow changes, in that this effect occurs even in diabetic patients who showed no changes in these variables.
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Original Articles|
January 01 1989
Kidney Hemodynamics After Ketone Body and Amino Acid Infusion in Normal and IDDM Subjects
Romano Nosadini;
Romano Nosadini
Institutes of Internal Medicine and Clinical Medicine, University of Padova
Padova, Italy
Centro Diabetico di Monfalcone
di Pordenone, and di Belluno, Padua, Italy
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Roberto Trevisan;
Roberto Trevisan
Institutes of Internal Medicine and Clinical Medicine, University of Padova
Padova, Italy
Centro Diabetico di Monfalcone
di Pordenone, and di Belluno, Padua, Italy
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Paolo Fioretto;
Paolo Fioretto
Institutes of Internal Medicine and Clinical Medicine, University of Padova
Padova, Italy
Centro Diabetico di Monfalcone
di Pordenone, and di Belluno, Padua, Italy
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Andrea Semplicini;
Andrea Semplicini
Institutes of Internal Medicine and Clinical Medicine, University of Padova
Padova, Italy
Centro Diabetico di Monfalcone
di Pordenone, and di Belluno, Padua, Italy
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Bruno Samà;
Bruno Samà
Institutes of Internal Medicine and Clinical Medicine, University of Padova
Padova, Italy
Centro Diabetico di Monfalcone
di Pordenone, and di Belluno, Padua, Italy
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Mario Velussi;
Mario Velussi
Institutes of Internal Medicine and Clinical Medicine, University of Padova
Padova, Italy
Centro Diabetico di Monfalcone
di Pordenone, and di Belluno, Padua, Italy
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Gian Luigi Da Campo;
Gian Luigi Da Campo
Institutes of Internal Medicine and Clinical Medicine, University of Padova
Padova, Italy
Centro Diabetico di Monfalcone
di Pordenone, and di Belluno, Padua, Italy
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Angelo Avogaro;
Angelo Avogaro
Institutes of Internal Medicine and Clinical Medicine, University of Padova
Padova, Italy
Centro Diabetico di Monfalcone
di Pordenone, and di Belluno, Padua, Italy
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Andrea Vizzaccaro;
Andrea Vizzaccaro
Institutes of Internal Medicine and Clinical Medicine, University of Padova
Padova, Italy
Centro Diabetico di Monfalcone
di Pordenone, and di Belluno, Padua, Italy
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Valter Donadon;
Valter Donadon
Institutes of Internal Medicine and Clinical Medicine, University of Padova
Padova, Italy
Centro Diabetico di Monfalcone
di Pordenone, and di Belluno, Padua, Italy
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Sandro Mongillo;
Sandro Mongillo
Institutes of Internal Medicine and Clinical Medicine, University of Padova
Padova, Italy
Centro Diabetico di Monfalcone
di Pordenone, and di Belluno, Padua, Italy
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Alessandro Doria
Alessandro Doria
Institutes of Internal Medicine and Clinical Medicine, University of Padova
Padova, Italy
Centro Diabetico di Monfalcone
di Pordenone, and di Belluno, Padua, Italy
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Address correspondence and reprint requests to R. Nosadini, Istituto di Medicina Interna, Patologia Medica I, Policlinico Universitario, Via Giustiniani, 2–35128 Padua, Italy.
Diabetes 1989;38(1):75–83
Article history
Received:
August 10 1987
Revision Received:
July 08 1988
Accepted:
July 08 1988
PubMed:
2909415
Citation
Romano Nosadini, Roberto Trevisan, Paolo Fioretto, Andrea Semplicini, Bruno Samà, Mario Velussi, Gian Luigi Da Campo, Angelo Avogaro, Andrea Vizzaccaro, Valter Donadon, Sandro Mongillo, Alessandro Doria; Kidney Hemodynamics After Ketone Body and Amino Acid Infusion in Normal and IDDM Subjects. Diabetes 1 January 1989; 38 (1): 75–83. https://doi.org/10.2337/diab.38.1.75
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