Literature DB >> 7459673

A Na+,K+ co-transport assay for essential hypertension.

G Dagher, R P Garay.   

Abstract

In erythrocytes from essential hypertensive patients and some of their normotensive offspring, the Na+,K+ co-transport system is unable to transport Na+ in an uphill direction against the electrochemical Na+ gradient. Recent studies of the kinetic properties of this system have permitted us to further characterize the abnormal co-transport in hypertension. Thirty-four essential hypertensive patients were characterized by a two- to three-fold decrease in the maximal rate of the outward Na+,K+ co-transport and a partial uncoupling of this system as compared with 22 normotensive controls. On the other hand, a normal co-transport was found in five secondary hypertensives with no family history of hypertension, thus indicating that the abnormal co-transport is not the consequence of high blood pressure per se. An abnormal co-transport was also found in around 50% of 19 young normotensives born of one hypertensive parent, suggesting genetic transmission. This study allows us to propose the use of a specific Na+,K+ co-transport assay for the differential diagnosis between essential and secondary hypertension and for the detection of those normotensives born of hypertensive parents with a potential risk to develop high blood pressure.

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Year:  1980        PMID: 7459673     DOI: 10.1139/o80-144

Source DB:  PubMed          Journal:  Can J Biochem        ISSN: 0008-4018


  11 in total

1.  Hypertension symposium: newer topics on normal and abnormal blood pressure regulatory mechanisms.

Authors:  M L Tuck; M S Golub; P Eggena; J R Sowers; M Maxwell
Journal:  West J Med       Date:  1983-08

Review 2.  Essential hypertension in blacks: epidemiology, characteristics, and possible roles of racial differences in sodium, potassium, and calcium regulation.

Authors:  A Aviv; M Aladjem
Journal:  Cardiovasc Drugs Ther       Date:  1990-03       Impact factor: 3.727

3.  The dependence on chloride ions of the loop diuretic sensitive component of passive sodium efflux from human red cells.

Authors:  D B Shennan; A R Chipperfield
Journal:  Pflugers Arch       Date:  1986-03       Impact factor: 3.657

4.  The Na+/K+ co-transport system in erythrocytes from pregnant patients.

Authors:  L Heilmann; G F von Tempelhoff; S Ulrich
Journal:  Arch Gynecol Obstet       Date:  1993       Impact factor: 2.344

5.  The effect of furosemide on sodium movements in human red blood cells.

Authors:  S C Brand; R Whittam
Journal:  J Physiol       Date:  1984-03       Impact factor: 5.182

6.  Ouabain-resistant Na+, K+ transport system in mouse NIH 3T3 cells.

Authors:  H Atlan; D Snyder; R Panet
Journal:  J Membr Biol       Date:  1984       Impact factor: 1.843

7.  Purification from human plasma of endogenous sodium transport inhibitor(s).

Authors:  J F Cloix; G Dagher; M Crabos; M G Pernollet; P Meyer
Journal:  Experientia       Date:  1984-12-15

8.  Ouabain-like activity in human cerebrospinal fluid.

Authors:  J Halperín; R Schaeffer; L Galvez; S Malavé
Journal:  Proc Natl Acad Sci U S A       Date:  1983-10       Impact factor: 11.205

9.  Modulation of Na+ transport systems in Wistar rat erythrocytes by excess dietary Na+ intake.

Authors:  M De Mendonça; M L Grichois; G Dagher; R Garay; P Meyer
Journal:  Pflugers Arch       Date:  1983-06       Impact factor: 3.657

10.  Sodium-potassium cotransport activity as genetic marker in essential hypertension.

Authors:  J S Davidson; L H Opie; B Keding
Journal:  Br Med J (Clin Res Ed)       Date:  1982-02-20
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