Aquaporin 2 expression increased by glucagon in normal rat inner medullary collecting ducts
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
19/10/2012
19/10/2012
2009
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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 |
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 |