Aquaporin 2 expression increased by glucagon in normal rat inner medullary collecting ducts


Autoria(s): YANO, Yuristella; CESAR, Katia R.; ARAUJO, Magali; RODRIGUES JR., Adilson C.; ANDRADE, Lucia C.; MAGALDI, Antonio J.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2009

Resumo

Yano Y, Cesar KR, Araujo M, Rodrigues Jr. AC, Andrade LC, Magaldi AJ. Aquaporin 2 expression increased by glucagon in normal rat inner medullary collecting ducts. Am J Physiol Renal Physiol 296: F54-F59, 2009. First published October 1, 2008; doi: 10.1152/ajprenal.90367.2008.-It is well known that Glucagon (Gl) is released after a high protein diet and participates in water excretion by the kidney, principally after a protein meal. To study this effect in in vitro perfused inner medullary collecting ducts (IMCD), the osmotic water permeability (Pf; mu m/s) at 37 degrees C and pH 7.4 in normal rat IMCDs (n = 36) perfused with Ringer/HCO(3) was determined. Gl (10(-7) M) in absence of Vasopressin (AVP) enhanced the Pf from 4.38 +/- 1.40 to 11.16 +/- 1.44 mu m/s (P < 0.01). Adding 10(-8), 10(-7), and 10(-6) M Gl, the Pf responded in a dose-dependent manner. The protein kinase A inhibitor H8 blocked the Gl effect. The specific Gl inhibitor, des-His(1)-[Glu(9)] glucagon (10(-7) M), blocked the Gl-stimulated Pf but not the AVP-stimulated Pf. There occurred a partial additional effect between Gl and AVP. The cAMP level was enhanced from the control 1.24 +/- 0.39 to 59.70 +/- 15.18 fm/mg prot after Gl 10(-7) M in an IMCD cell suspension. The immunoblotting studies indicated an increase in AQP2 protein abundance of 27% (cont 100.0 +/- 3.9 vs. Gl 127.53; P = 0.0035) in membrane fractions extracted from IMCD tubule suspension, incubated with 10(-6) M Gl. Our data showed that 1) Gl increased water absorption in a dose-dependent manner; 2) the anti-Gl blocked the action of Gl but not the action of AVP; 3) Gl stimulated the cAMP generation; 4) Gl increased the AQP2 water channel protein expression, leading us to conclude that Gl controls water absorption by utilizing a Gl receptor, rather than a AVP receptor, increasing the AQP2 protein expression.

Conselho Nacional de Pesquisa (CNPq

CNPq National Counsel for Scientific and Technological Development)

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo FAPESP

Foundation

Fundacao Faculdade de Medicina (FFM

School of Medicine Foundation)

Laboratorios de Investigacao Medica do Hospital das Clinicas da Faculdade de Medicina da Universidade de Sao Paulo FM-USP

Identificador

AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, v.296, n.1, p.F54-F59, 2009

1931-857X

http://producao.usp.br/handle/BDPI/26916

10.1152/ajprenal.90367.2008

http://dx.doi.org/10.1152/ajprenal.90367.2008

Idioma(s)

eng

Publicador

AMER PHYSIOLOGICAL SOC

Relação

American Journal of Physiology-renal Physiology

Direitos

restrictedAccess

Copyright AMER PHYSIOLOGICAL SOC

Palavras-Chave #glucagon #aquaporin 2 #water transport #glucagon antagonist #vasopressin #HENLES LOOP #TRANSPORT #WATER #UREA #KIDNEY #SUBSEGMENTS #ACTIVATION #POTASSIUM #EXCRETION #CHLORIDE #Physiology #Urology & Nephrology
Tipo

article

original article

publishedVersion