Literature DB >> 129330

Tubular Na, K-ATPase deficiency, the cause of the congenital renal salt-losing syndrome.

J R Bierich, U Schmidt.   

Abstract

In the serum of two infant sisters with a congenital renal salt-losing syndrome, Na was rather low and K considerably increased. Even with Na levels of 126 mval/1, sodium was excreted in the urine. Creatinine and hippurate clearances were normal. Primary disturbances of the steroid metabolism were not detectable; plasma cortisol was normal, aldosterone and renin were compensatorily increased. Treatment with DOCA was unsuccessful. Whereas the first infant died (in another hospital), the second one throve well with high oral substitution of NaCl. There was no pathological findings other than a moderate hyperplasia of the juxtaglomerular apparatus, in a kidney biopsy. Except for minimal activity in the ascending limb of Henle's loop, there was no membrane bound Na, K-ATPase in the microdissected tubules. This finding most probably explains the renal salt loss, as this enzyme is necessary for the transcellular flow of sodium and potassium.

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Year:  1976        PMID: 129330     DOI: 10.1007/bf00443063

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  4 in total

1.  AN ALDOSTERONE BIOSYNTHETIC DEFECT IN A SALT-LOSING DISORDER.

Authors:  S ULICK; E GAUTIER; K K VETTER; J R MARKELLO; S YAFFE; C U LOWE
Journal:  J Clin Endocrinol Metab       Date:  1964-07       Impact factor: 5.958

2.  A NEW HEREDITARY DEFECT IN THE BIOSYNTHESIS OF ALDOSTERONE: URINARY C21-CORTICOSTEROID PATTERN IN THREE RELATED PATIENTS WITH A SALT-LOSING SYNDROME, SUGGESTING AN 18-OXIDATION DEFECT.

Authors:  H K VISSER; W S COST
Journal:  Acta Endocrinol (Copenh)       Date:  1964-12

3.  Activity of (Na+K+)-stimulated adenosintriphosphatase in the rat nephron.

Authors:  U Schmidt; U C Dubach
Journal:  Pflugers Arch       Date:  1969       Impact factor: 3.657

4.  The function of Na, K-ATPase in single portions of the rat nephron.

Authors:  U Schmidt; H Schmid; B Funk; U C Dubach
Journal:  Ann N Y Acad Sci       Date:  1974       Impact factor: 5.691

  4 in total
  8 in total

1.  Long term observations in a patient with pseudohypoaldosteronism.

Authors:  R J Hogg; J F Marks; D Marver; J C Frolich
Journal:  Pediatr Nephrol       Date:  1991-03       Impact factor: 3.714

2.  Reversible renal resistance to aldosterone associated with interstitial nephritis.

Authors:  J J Regan; C S Greenberg; A D Mooradian; N Staley; F Q Nuttall
Journal:  West J Med       Date:  1987-06

3.  Pseudohypoaldosteronism. Response to long-term treatment with indomethacin.

Authors:  M Bommen; C G Brook
Journal:  Arch Dis Child       Date:  1982-09       Impact factor: 3.791

4.  [Primary hypoaldosteronism, pseudo-hypoaldosteronism and distal tubular acidosis].

Authors:  D Klaus
Journal:  Klin Wochenschr       Date:  1984-08-16

5.  Pseudohypoaldosteronism in a child with Down syndrome. Long-term management of salt loss by ion exchange resin administration.

Authors:  H Saule; H G Dörr; W G Sippell
Journal:  Eur J Pediatr       Date:  1984-09       Impact factor: 3.183

6.  [Primary hypoaldosteronism and secondary pseudo-hypoaldosteronism].

Authors:  D Klaus; R M Lederle; P Vecsei
Journal:  Klin Wochenschr       Date:  1984-08-16

7.  Pseudohypoaldosteronism.

Authors:  M J Dillon; J V Leonard; J M Buckler; D Ogilvie; D Lillystone; J W Honour; C H Shackleton
Journal:  Arch Dis Child       Date:  1980-06       Impact factor: 3.791

Review 8.  The central mechanism underlying hypertension: a review of the roles of sodium ions, epithelial sodium channels, the renin-angiotensin-aldosterone system, oxidative stress and endogenous digitalis in the brain.

Authors:  Hakuo Takahashi; Masamichi Yoshika; Yutaka Komiyama; Masato Nishimura
Journal:  Hypertens Res       Date:  2011-08-04       Impact factor: 3.872

  8 in total

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