Posttranslational mechanisms associated with reduced NHE3 activity in adult vs. young prehypertensive SHR
| Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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| Data(s) |
19/10/2012
19/10/2012
2010
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| Resumo |
Crajoinas RO, Lessa LMA, Carraro-Lacroix LR, Davel APC, Pacheco BPM, Rossoni LV, Malnic G, Girardi ACC. Posttranslational mechanisms associated with reduced NHE3 activity in adult vs. young prehypertensive SHR. Am J Physiol Renal Physiol 299:F872-F881, 2010. First published July 14, 2010; doi:10.1152/ajprenal.00654.2009.-Abnormalities in renal proximal tubular (PT) sodium transport play an important role in the pathophysiology of essential hypertension. The Na(+)/H(+) exchanger isoform 3 (NHE3) represents the major route for sodium entry across the apical membrane of renal PT cells. We therefore aimed to assess in vivo NHE3 transport activity and to define the molecular mechanisms underlying NHE3 regulation before and after development of hypertension in the spontaneously hypertensive rat (SHR). NHE3 function was measured as the rate of bicarbonate reabsorption by means of in vivo stationary microperfusion in PT from young prehypertensive SHR (Y-SHR; 5-wk-old), adult SHR (A-SHR; 14-wk-old), and age-matched Wistar Kyoto (WKY) rats. We found that NHE3-mediated PT bicarbonate reabsorption was reduced with age in the SHR (1.08 +/- 0.10 vs. 0.41 +/- 0.04 nmol/cm(2)xs), while it was increased in the transition from youth to adulthood in the WKY rat (0.59 +/- 0.05 vs. 1.26 +/- 0.11 nmol/cm(2)xs). Higher NHE3 activity in the Y-SHR compared with A-SHR was associated with a predominant microvilli confinement and a lower ratio of phosphorylated NHE3 at serine-552 to total NHE3 (P-NHE3/total). After development of hypertension, P-NHE3/total increased and NHE3 was retracted out of the microvillar microdomain along with the regulator dipeptidyl peptidase IV (DPPIV). Collectively, our data suggest that the PT is playing a role in adapting to the hypertension in the SHR. The molecular mechanisms of this adaptation possibly include an increase of P-NHE3/total and a redistribution of the NHE3-DPPIV complex from the body to the base of the PT microvilli, both predicted to decrease sodium reabsorption. FAPESP Fundacao de Amparo a Pesquisa do Estado de Sao Paulo CNPq Conselho Nacional de Desenvolvimento Cientifico e Tecnologico |
| Identificador |
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, v.299, n.4, p.F872-F881, 2010 1931-857X http://producao.usp.br/handle/BDPI/22948 10.1152/ajprenal.00654.2009 |
| Idioma(s) |
eng |
| Publicador |
AMER PHYSIOLOGICAL SOC |
| Relação |
American Journal of Physiology-renal Physiology |
| Direitos |
restrictedAccess Copyright AMER PHYSIOLOGICAL SOC |
| Palavras-Chave | #sodium transport #proximal tubule #blood pressure #phosphorylation #dipeptidyl peptidase IV #GLUCAGON-LIKE PEPTIDE-1 #SPONTANEOUSLY HYPERTENSIVE RAT #NA+/H+ EXCHANGER ISOFORM #RENAL PROXIMAL TUBULE #CAMP-MEDIATED INHIBITION #BRUSH-BORDER #SUBCELLULAR-DISTRIBUTION #REGULATORY PROTEIN #MEMBRANE-VESICLES #NEPHRON FUNCTION #Physiology #Urology & Nephrology |
| Tipo |
article original article publishedVersion |