Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/111833
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Type: Journal article
Title: Antihypertensive and laxative effects by pharmacological inhibition of sodium-proton-exchanger subtype 3-Mediated sodium absorption in the gut
Author: Linz, D.
Wirth, K.
Linz, W.
Heuer, H.
Frick, W.
Hofmeister, A.
Heinelt, U.
Arndt, P.
Schwahn, U.
Böhm, M.
Ruetten, H.
Citation: Hypertension, 2012; 60(6):1560-1567
Publisher: American Heart Association
Issue Date: 2012
ISSN: 0194-911X
1524-4563
Statement of
Responsibility: 
Dominik Linz, Klaus Wirth, Wolfgang Linz, Hubert O. O. Heuer, Wendelin Frick, Armin Hofmeister, Uwe Heinelt, Petra Arndt, Uwe Schwahn, Michael Böhm, Hartmut Ruetten
Abstract: High intestinal sodium absorption is one mechanism of hypertension and constipation. The sodium-proton-exchanger subtype 3 (NHE3) is an important mediator of sodium absorption in the gut. SAR218034 (SAR) is an orally nonabsorbable specific NHE3 inhibitor. The effect of SAR (1 mg/kg per day in chow) on feces sodium excretion, systolic blood pressure via tail cuff, and gene expression of NHE3 in the gut were studied in senescent lean hypertensive rats (spontaneously hypertensive rats-lean, loaded with NaCl 0.7% in drinking water) and in hypertensive, obese, and hyperinsulinemic rats (spontaneously hypertensive rats-obese, not loaded with NaCl). In spontaneously hypertensive rats-lean, inhibition of intestinal NHE3 by SAR increased feces sodium excretion and reduced urinary sodium excretion, whereas absolute sodium balance and serum sodium concentration were not changed. This suggests reduced intestinal sodium absorption in SAR-treated animals and was associated with increased feces water content (58% versus 42% in placebo treated animals; P=0.0001) and reduction in systolic blood pressure from 222 ± 7 to 198 ± 2 mm Hg (P=0.0001). Angiotensin-converting enzyme inhibition by ramipril plus NHE3 inhibition resulted in an additive blood pressure-lowering effect. In spontaneously hypertensive rats-obese, SAR lowered systolic blood pressure but did not modify serum insulin or cholesterol levels. Gene expression of NHE3 was upregulated in the ileum and colon but not in the jejunum of SAR-treated rats. Reduction of intestinal sodium absorption by selective NHE3 inhibition in the gut reduces high blood pressure and increases feces water excretion. Intestinal NHE3 blockade could be a new treatment strategy for elderly patients suffering from high blood pressure and constipation.
Keywords: sodium-proton-exchanger subtype 3 inhibition; intestinal sodium absorption; constipation blood pressure; spontaneously hypertensive rats; obese spontaneously hypertensive rats
Rights: © 2012 American Heart Association, Inc.
DOI: 10.1161/HYPERTENSIONAHA.112.201590
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