AI Article Synopsis

  • Several abnormalities in sodium (Na) metabolism are linked to the development of essential hypertension, with evidence suggesting alterations in Na transport systems in the red blood cell membranes of affected patients.
  • The study evaluated four distinct Na transport systems in red cell membranes across three groups: normotensive controls, normotensive individuals with a family history of hypertension, and essential hypertensive patients.
  • Findings indicated significant decreases in Na-K cotransport in both hypertensive and family-history groups, with around 90.9% of individuals in these groups showing abnormalities in one or more Na transport systems, highlighting the potential role of these alterations in hypertension development.

Article Abstract

Several abnormalities in Na metabolism have been implicated in the pathogenesis of essential hypertension. In addition, recent work by several investigators has showed that some Na transport systems in red cell membranes may be altered in those patients. In order to confirm such abnormalities we evaluated simultaneously four different and clearly defined Na transport systems in red cell membranes: the ouabain sensitive Na pump (P) and the Na-K cotransport (Co) in nystatin loaded cells, the maximal rate of Na-Li countertransport (CTT) in lithium loaded cells and the rate constant of Na passive permeability (pp) in 58 normotensive control subjects with no family history of hypertension (N), 19 normotensive subjects with family history of hypertension (NH) and 34 essential hypertensive patients (HE). The mean (mean +/- SEM microns/lc/h) value of the P and pp was found to be comparable in the three groups. Co was found significantly decreased in both HE (241 +/- 28) and in NH (227 +/- 42) when compared to the control group (290 +/- 10). Although NH also showed CTT values (377 +/- 87) higher than controls, the difference did not reach statistical significance. Our results indicate that approximately 90.9% of both HE and NH presented abnormalities in one or more of the various Na transport systems studied. Normotensive patients with a positive family history and alterations in some of the Na transport systems in red cell membranes may prove an interesting experimental model to assess the importance of such alterations for the development of hypertension.

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