Plasma Ouabain-Like Factor During Acute and Chronic Changes in Sodium Balance in Essential Hypertension

Author:

Manunta Paolo1,Messaggio Elisabetta1,Ballabeni Cinzia1,Sciarrone Maria Teresa1,Lanzani Chiara1,Ferrandi Mara1,Hamlyn John M.1,Cusi Daniele1,Galletti Ferruccio1,Bianchi Giuseppe1,

Affiliation:

1. From the Division of Nephrology, Dialysis, and Hypertension, University “Vita Salute San Raffaele” (P.M., E.M., C.B., M.T.S., C.L.), Milan, Italy; Prassis Research Institute Sigma-Tau, Settimo Milanese (M.F.), Milan, Italy; Department of Physiology, School of Medicine, University of Maryland (J.M.H.), Baltimore; Division of Nephrology University of Milan (D.C.), Milan, Italy; Department of Experimental Medicine, University of Naples, Federico II (F.G.), Naples, Italy.

Abstract

An ouabain-like factor has been implicated repeatedly in salt-sensitive hypertension as a natriuretic agent. However, the response of plasma ouabain-like factor to acute and chronic variation of body sodium is unclear. We studied 138 patients with essential hypertension who underwent an acute volume expansion/contraction maneuver (2 days) and 20 patients who entered a blind randomized crossover design involving chronically controlled sodium intake and depletion (170 to 70 mmol/d; 2 weeks each period). In both studies, plasma levels of ouabain-like factor were higher during sodium depletion (acute: 338.8±17.4 and 402.7±22.8 pmol/L for baseline and low sodium, respectively, P <0.01; chronic: 320.4±32.0 versus 481.0±48.1 pmol/L, P =0.01). No significant change in plasma ouabain-like factor was observed after a 2-hour saline infusion (333.4±23.9 pmol/L) or controlled sodium (402.1±34.9 pmol/L). When patients were divided into salt-sensitive or salt-resistant groups, no differences in plasma ouabain-like factor were observed in the 2 groups at baseline or in response to the 2 protocols: salt resistant (n=69, 340.1±25.9 pmol/L) versus salt sensitive (n=69, 337.4±23.6 pmol/L) and chronic salt resistant (n=11, 336.0±53.2) versus salt sensitive (n=9, 301.1±331.4 pmol/L). However, circulating ouabain-like factor was increased by sodium depletion in both groups. These results demonstrate that circulating ouabain-like factor is raised specifically by maneuvers that promote the loss of body sodium. Acute expansion of body fluids with isotonic saline is not a stimulus to plasma ouabain-like factor. Moreover, basal levels of plasma ouabain-like factor do not differ among patients with salt-sensitive or salt-resistant hypertension. Taken together, these new results suggest that ouabain-like factor is involved in the adaptation of humans to sodium depletion and argue against the hypothesis that ouabain-like factor is a natriuretic hormone.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Internal Medicine

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