4.6 Article

Guanine-induced inhibition of renal Na+-ATPase activity: Evidence for the involvement of the Gi protein-coupled receptor

Journal

ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS
Volume 513, Issue 2, Pages 126-130

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.abb.2011.07.007

Keywords

Renal purine; Guanine; Sodium pump; G protein; Cell signaling; Proximal tubule

Funding

  1. FAPERJ
  2. Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)
  3. Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES)
  4. Fundacao Carlos Chagas Filho de Amparo a Pesquisa do Estado do Rio de Janeiro (FAPERJ)
  5. Instituto Nacional de Ciencia e Tecnologia em Biologia Estrutural e Bioimagem (INBEB/CNPq)

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There is some evidence to show a possible role of guanosine in the modulation of cellular function, in particular, in the neuronal system. However, nothing is known about the role of guanine in renal function. The aim of the present work was to investigate the role of guanine on modulation of Na+-ATPase activity in isolated basolateral membrane (BLM) of the renal cortex. Guanine inhibited the enzyme activity in a dose-dependent manner with maximal effect (56%) obtained at 10(-6) M. This effect was reversed by DPCPX (8-cyclopentyl-1,3-dipropylxanthine), an antagonist of A(1) receptors, but it was not changed by 10(-8) M DMPX (3,7-dimethyl-1-propargylxanthine) or 10(-8) M MRS (2,3-diethyl-4,5-dipropyl-6-phenyl-pyridine-3-thiocarboxylate-5-carboxylate), antagonists of A(2) and A(3) receptors, respectively. Furthermore, it was observed that guanine increased [gamma-S-35]GTP-specific binding with the maximal effect observed at 10(-6) M and this effect was abolished by 10(-8) M GDP beta S. The inhibitory effect of 10(-8) M guanine on Na+-ATPase activity was reversed by 10(-6) M GDP beta S, 10(-6) M forskolin, 10(-6) M pertussis toxin and 10(-8) M cholera toxin. These results indicate that guanine binds to a DPCPX-sensitive receptor promoting the activation of Gi protein and leading to a decrease in cAMP level and, consequently, inhibition of BLM Na+-ATPase activity. (C) 2011 Elsevier Inc. All rights reserved.

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