Mechanisms underlying the inhibitory effects of uroguanylin on NHE3 transport activity in renal proximal tubule
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
14/10/2013
14/10/2013
2012
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Resumo |
Lessa LM, Carraro-Lacroix LR, Crajoinas RO, Bezerra CN, Dariolli R, Girardi AC, Fonteles MC, Malnic G. Mechanisms underlying the inhibitory effects of uroguanylin on NHE3 transport activity in renal proximal tubule. Am J Physiol Renal Physiol 303: F1399-F1408, 2012. First published September 5, 2012; doi: 10.1152/ajprenal.00385.2011.-We previously demonstrated that uroguanylin (UGN) significantly inhibits Na+/H+ exchanger (NHE)3-mediated bicarbonate reabsorption. In the present study, we aimed to elucidate the molecular mechanisms underlying the action of UGN on NHE3 in rat renal proximal tubules and in a proximal tubule cell line (LLC-PK1). The in vivo studies were performed by the stationary microperfusion technique, in which we measured H+ secretion in rat renal proximal segments, through a H+-sensitive microelectrode. UGN (1 mu M) significantly inhibited the net of proximal bicarbonate reabsorption. The inhibitory effect of UGN was completely abolished by either the protein kinase G (PKG) inhibitor KT5823 or by the protein kinase A (PKA) inhibitor H-89. The effects of UGN in vitro were found to be similar to those obtained by microperfusion. Indeed, we observed that incubation of LLC-PK1 cells with UGN induced an increase in the intracellular levels of cAMP and cGMP, as well as activation of both PKA and PKG. Furthermore, we found that UGN can increase the levels of NHE3 phosphorylation at the PKA consensus sites 552 and 605 in LLC-PK1 cells. Finally, treatment of LLC-PK1 cells with UGN reduced the amount of NHE3 at the cell surface. Overall, our data suggest that the inhibitory effect of UGN on NHE3 transport activity in proximal tubule is mediated by activation of both cGMP/PKG and cAMP/PKA signaling pathways which in turn leads to NHE3 phosphorylation and reduced NHE3 surface expression. Moreover, this study sheds light on mechanisms by which guanylin peptides Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) Conselho Nacional de Pesquisas (CNPq) Conselho Nacional de Pesquisas (CNPq) Fund. C. Fortaleza (Funcap) Fund. C. Fortaleza (Funcap) |
Identificador |
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, BETHESDA, v. 303, n. 10, supl. 1, Part 6, pp. F1399-F1408, NOV, 2012 1931-857X http://www.producao.usp.br/handle/BDPI/34338 10.1152/ajprenal.00385.2011 |
Idioma(s) |
eng |
Publicador |
AMER PHYSIOLOGICAL SOC BETHESDA |
Relação |
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY |
Direitos |
closedAccess Copyright AMER PHYSIOLOGICAL SOC |
Palavras-Chave | #NHE3 #UROGUANYLIN #RENAL MICROPERFUSION #BICARBONATE REABSORPTION #CGMP #CAMP #HEAT-STABLE ENTEROTOXIN #INTESTINAL GUANYLATE-CYCLASE #MESSENGER-RNA EXPRESSION #NA+/H+ EXCHANGER ISOFORM #PROTEIN-KINASE #MICE LACKING #NATRIURETIC RESPONSE #SODIUM-TRANSPORT #DIETARY SALT #NITRIC-OXIDE #PHYSIOLOGY #UROLOGY & NEPHROLOGY |
Tipo |
article original article publishedVersion |