Increased NHE3 abundance and transport activity in renal proximal tubule of rats with heart failure


Autoria(s): Inoue, Bruna Hitomi; dos Santos, Leonardo; Pessoa, Thaíssa Dantas; Antonio, Ednei L.; Pacheco, Bruna P. M.; Savignano, Fernanda A.; Carraro-Lacroix, Luciene R.; Tucci, Paulo J. F.; Malnic, Gerhard; Girardi, Adriana Castello Costa
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

05/11/2013

05/11/2013

2012

Resumo

Inoue BH, dos Santos L, Pessoa TD, Antonio EL, Pacheco BPM, Savignano FA, Carraro-Lacroix LR, Tucci PJF, Malnic G, Girardi ACC. Increased NHE3 abundance and transport activity in renal proximal tubule of rats with heart failure. Am J Physiol Regul Integr Comp Physiol 302: R166-R174, 2012. First published October 26, 2011; doi:10.1152/ajpregu.00127.2011.-Heart failure (HF) is associated with a reduced effective circulating volume that drives sodium and water retention and extracellular volume expansion. We therefore hypothesized that Na(+)/H(+) exchanger isoform 3 (NHE3), the major apical transcellular pathway for sodium reabsorption in the proximal tubule, is upregulated in an experimental model of HF. HF was induced in male rats by left ventricle radiofrequency ablation. Sham-operated rats (sham) were used as controls. At 6 wk after surgery, HF rats exhibited cardiac dysfunction with a dramatic increase in left ventricular end-diastolic pressure. By means of stationary in vivo microperfusion and pH-dependent sodium uptake, we demonstrated that NHE3 transport activity was significantly higher in the proximal tubule of HF compared with sham rats. Increased NHE3 activity was paralleled by increased renal cortical NHE3 expression at both protein and mRNA levels. In addition, the baseline PKA-dependent NHE3 phosphorylation at serine 552 was reduced in renal cortical membranes of rats with HF. Collectively, these results suggest that NHE3 is upregulated in the proximal tubule of HF rats by transcriptional, translational, and posttranslational mechanisms. Enhanced NHE3-mediated sodium reabsorption in the proximal tubule may contribute to extracellular volume expansion and edema, the hallmark feature of HF. Moreover, our study emphasizes the importance of undertaking a cardiorenal approach to contain progression of cardiac disease.

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico

Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior

Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior

Identificador

AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, BETHESDA, v. 302, n. 1, supl. 1, Part 6, pp. R166-R174, JAN, 2012

0363-6119

http://www.producao.usp.br/handle/BDPI/41033

10.1152/ajpregu.00127.2011

http://dx.doi.org/10.1152/ajpregu.00127.2011

Idioma(s)

eng

Publicador

AMER PHYSIOLOGICAL SOC

BETHESDA

Relação

AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY

Direitos

restrictedAccess

Copyright AMER PHYSIOLOGICAL SOC

Palavras-Chave #MYOCARDIAL INJURY #RENAL FUNCTION #VOLUME HOMEOSTASIS #RADIOFREQUENCY ABLATION #ATRIAL-NATRIURETIC-PEPTIDE #NA+/H+ EXCHANGER NHE3 #SPONTANEOUSLY HYPERTENSIVE RAT #ANGIOTENSIN-ALDOSTERONE SYSTEM #ACUTE MYOCARDIAL-INFARCTION #THICK ASCENDING LIMB #UNIFYING HYPOTHESIS #EXTRACELLULAR FLUID #SODIUM RETENTION #EPITHELIAL-CELLS #PHYSIOLOGY
Tipo

article

original article

publishedVersion