Literature DB >> 4600043

Renal handling of diamino acids in lysinuric protein intolerance.

O Simell, J Perheentupa.   

Abstract

Lysinuric protein intolerance (LPI) is a rare recessively inherited disease in which one of the fundamental physiological defects is in the mechanism by which diamino acids are transported by the kidney. The purpose of the present studies was to examine that mechanism in four controls and seven patients with LPI. Two types of studies were conducted. In the first set, the renal handling of l-arginine and l-ornithine was evaluated by gradually increasing the plasma concentration of each of these amino acids by constant infusion techniques. In the second set of studies, the possible existence of competitive inhibition between l-arginine, l-ornithine, and l-lysine was examined. In the control subjects, there was almost complete reabsorption of arginine and ornithine, with increases in their filtered loads to 50-100 times normal. With further increases in the filtered loads of these amino acids, there was a gradual decrease in their fractional reabsorption. Mutual competitive inhibition was suggested by the observation that an increase in the filtered load of one diamino acid was associated with a decrease in the reabsorption of the other two. In LPI, the fasting plasma diamino acid concentrations were significantly lower than in the controls. With low filtered loads, the fractional reabsorption of the diamino acids was clearly below normal. This defect diminished with higher loads. A stepwise increase in the plasma concentration of one diamino acid resulted in a biphasic response. Initially, net tubular secretion of the other diamino acids was noted, but later was followed by return to net absorption. When two diamino acids were infused simultaneously, net absorption of both took place, though less efficiently than in the controls. We conclude that the renal reabsorption mechanism is defective in patients with LPI. With low normal filtered loads, there is increased fractional excretion of all three diamino acids resulting in low serum concentrations of these compounds. However, at higher artificially elevated concentrations of diamino acids, the capacity of the renal transport system in these patients appears normal.

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Year:  1974        PMID: 4600043      PMCID: PMC301519          DOI: 10.1172/JCI107753

Source DB:  PubMed          Journal:  J Clin Invest        ISSN: 0021-9738            Impact factor:   14.808


  23 in total

1.  Comparison between inulin and 51Cr-labelled edetic acid for the measurement of glomerular filtration-rate.

Authors:  D A Heath; M S Knapp; W H Walker
Journal:  Lancet       Date:  1968-11-23       Impact factor: 79.321

2.  Familial protein intolerance with deficient transport of basic amino acids. Report on an adult patient with chronic hyperammonemia.

Authors:  M Kekomäki; E Toivakka; V Häkkinen; M Salaspuro
Journal:  Acta Med Scand       Date:  1968-04

3.  Congenital lysinuria: a new inherited transport disorder of dibasic amino acids.

Authors:  K Oyanagi; R Miura; T Yamanouchi
Journal:  J Pediatr       Date:  1970-08       Impact factor: 4.406

4.  Protein intolerance with deficient transport of basic aminoacids. Another inborn error of metabolism.

Authors:  J Perheentupa; J K Visakorpi
Journal:  Lancet       Date:  1965-10-23       Impact factor: 79.321

5.  Transport of diamino acids into the Ehrlich cell.

Authors:  H N Christensen; M Liang
Journal:  J Biol Chem       Date:  1966-12-10       Impact factor: 5.157

6.  A common renal transport system for lysine, ornithine, arginine and cysteine.

Authors:  L Schwartzman; A Blair; S Segal
Journal:  Biochem Biophys Res Commun       Date:  1966-04-19       Impact factor: 3.575

7.  Enzymes of urea synthesis in familial protein intolerance with deficient transport of basic amino acids.

Authors:  M Kekomäki; N C Räihä; J Perheentupa
Journal:  Acta Paediatr Scand       Date:  1967-11

8.  Familial protein intolerance with deficient transport of basic amino acids. An analysis of 10 patients.

Authors:  M Kekomäki; J K Visakorpi; J Perheentupa; L Saxén
Journal:  Acta Paediatr Scand       Date:  1967-11

9.  The renal clearance of amino acids in cystinuria.

Authors:  J C Crawhall; E F Scowen; C J Thompson; R W Watts
Journal:  J Clin Invest       Date:  1967-07       Impact factor: 14.808

10.  Lysine transport in human kidney: evidence for two systems.

Authors:  L E Rosenberg; I Albrecht; S Segal
Journal:  Science       Date:  1967-03-17       Impact factor: 47.728

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  14 in total

1.  Oral lysine feeding in gyrate atrophy with hyperornithinaemia--a pilot study.

Authors:  K Peltola; O J Heinonen; K Näntö-Salonen; K Pulkki; O Simell
Journal:  J Inherit Metab Dis       Date:  2000-06       Impact factor: 4.982

2.  Cloning and functional expression of a cDNA from rat jejunal epithelium encoding a protein (4F2hc) with system y+L amino acid transport activity.

Authors:  S Y Yao; W R Muzyka; J F Elliott; C I Cheeseman; J D Young
Journal:  Biochem J       Date:  1998-03-01       Impact factor: 3.857

3.  Lysinuric protein intolerance mutation is not expressed in the plasma membrane of erythrocytes.

Authors:  D W Smith; C R Scriver; O Simell
Journal:  Hum Genet       Date:  1988-12       Impact factor: 4.132

4.  Dibasic amino acid transport: lessons from human disease.

Authors:  S O Thier
Journal:  Trans Am Clin Climatol Assoc       Date:  1984

5.  Renal transport of lysine and arginine in lysinuric protein intolerance.

Authors:  T Kato; N Mizutani; M Ban
Journal:  Eur J Pediatr       Date:  1982-11       Impact factor: 3.183

6.  Gyrate atrophy of the choroid and retina: amino acid metabolism and correction of hyperornithinemia with an arginine-deficient diet.

Authors:  D Valle; M Walser; S W Brusilow; M Kaiser-Kupfer
Journal:  J Clin Invest       Date:  1980-02       Impact factor: 14.808

7.  Lysinuric protein intolerance mutation is expressed in the plasma membrane of cultured skin fibroblasts.

Authors:  D W Smith; C R Scriver; H S Tenenhouse; O Simell
Journal:  Proc Natl Acad Sci U S A       Date:  1987-11       Impact factor: 11.205

8.  Skeletal manifestations of lysinuric protein intolerance. A follow-up study of 29 patients.

Authors:  E Svedström; K Parto; M Marttinen; P Virtama; O Simell
Journal:  Skeletal Radiol       Date:  1993       Impact factor: 2.199

9.  Hyperdibasicaminoaciduria in a Turkish infant without evident protein intolerance.

Authors:  W Endres; G Zoulek; J Schaub
Journal:  Eur J Pediatr       Date:  1979-04-25       Impact factor: 3.183

10.  Lysinuric protein intolerance. Basolateral transport defect in renal tubuli.

Authors:  J Rajantie; O Simell; J Perheentupa
Journal:  J Clin Invest       Date:  1981-04       Impact factor: 14.808

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