Spironolactone inhibits the activity of the Na+/H+ exchanger in the aorta of mineralocorticoid-induced hypertensive rats

Juan E. Carreño, Fernando J. Verdugo, Felipe Contreras, Felipe A. Montellano, Sebastian Veloso, Kurt A. Schalper, Mauricio Sandoval, Sandra Villanueva, Elisa Marusic, Carlos E. Irarrazabal*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

6 Scopus citations


Introduction: Aldosterone can induce changes in the expression or activity of Na+/H+ exchanger isoform 1 (NHE-1) in vascular smooth muscle cells. We aimed to clarify whether chronic mineralocorticoid receptor activation exerts an effect on the activity of NHE-1 in the aorta of mineralocorticoid-induced hypertensive rats. Methods: Uninephrectomized male Sprague-Dawley rats received subcutaneously 10 mg/week of desoxycorticosterone (DOCA) with or without 20 mg/kg of spironolactone, or vehicle alone (n = 20). After four weeks of treatment, the animals were sacrificed; the aorta was excised for subsequent studies, including histological analysis, RT-PCR, Western blot, measurement of NHE-1 activity and vascular contractility in the presence or absence of the selective NHE-1 inhibitor ethyl-isopropyl amiloride (EIPA). Results: Chronic DOCA treatment increased the NHE-1 activity, systolic and diastolic blood pressure, and aortic wall thickness. All these effects were prevented by co-treatment with Spironolactone (p < 0.05). Phenylephrine-induced vascular contractility was significantly reduced in the DOCA group when EIPA was added in the media (p < 0.05). No significant differences in NHE-1 mRNA or protein levels were detected between groups. Conclusions: Chronic DOCA administration induced functional and morphological alterations in the rat aorta that are partially explained by enhanced NHE-1 activity and prevented by spironolactone. However, we did not observe changes in the NHE-1 transcript or protein levels, suggesting that the effect may be due to post-transcriptional modifications induced by mineralocorticoid receptor activation.

Original languageEnglish
Pages (from-to)1225-1231
Number of pages7
JournalJRAAS - Journal of the Renin-Angiotensin-Aldosterone System
Issue number4
StatePublished - 1 Dec 2015

Bibliographical note

Publisher Copyright:
© 2015 The Author(s).


  • Desoxycorticosterone
  • Mineralocorticoid receptor
  • Mineralocorticoid receptor antagonists
  • Sodium-hydrogen antiporter
  • Vasoconstriction


Dive into the research topics of 'Spironolactone inhibits the activity of the Na+/H+ exchanger in the aorta of mineralocorticoid-induced hypertensive rats'. Together they form a unique fingerprint.

Cite this