• DOI:10.1152/AJPRENAL.00172.2005
• Corpus ID: 13178869

Genetic ablation of Rhbg in the mouse does not impair renal ammonium excretion.

@article{Chambrey2005GeneticAO,
  title={Genetic ablation of Rhbg in the mouse does not impair renal ammonium excretion.},
  author={R{\'e}gine Chambrey and Dominique Goossens and Soline Bourgeois and Nicolas Picard and May Bloch-Faure and Françoise Leviel and Valerie Geoffroy and Mich{\`e}le Cambillau and Yves Colin and Michel Paillard and Pascal Houillier and Jean-Pierre Cartron and Dominique Eladari},
  journal={American journal of physiology. Renal physiology},
  year={2005},
  volume={289 6},
  pages={
          F1281-90
        }
}

• R. Chambrey, D. Goossens, +10 authors D. Eladari
• Published 1 December 2005
• Biology, Medicine
• American journal of physiology. Renal physiology

NH(4)(+) transport by the distal nephron and NH(4)(+) detoxification by the liver are critical for achieving regulation of acid-base balance and to avoid hyperammonemic hepatic encephalopathy, respectively. Therefore, it has been proposed that rhesus type B glycoprotein (Rhbg), a member of the Mep/Amt/Rh NH(3) channel superfamily, may be involved in some forms of distal tubular acidosis and congenital hyperammonemia. We have tested this hypothesis by inactivating the RHbg gene in the mouse by insertional mutagenesis. Histochemical studies analyses confirmed that RHbg knockout (KO) mice did not express Rhbg protein. Under basal conditions, the KO mice did not exhibit encephalopathy and survived well. They did not exhibit hallmarks of distal tubular acidosis because neither acid-base status, serum potassium concentration, nor bone mineral density was altered by RHbg disruption. They did not have hyperammonemia or disturbed hepatic NH(3) metabolism. Moreover, the KO mice adapted to a chronic acid-loading challenge by increasing urinary NH(4)(+) excretion as well as their wild-type controls. Finally, transepithelial NH(3) diffusive permeability, or NH(3) and NH(4)(+) entry across the basolateral membrane of cortical collecting duct cells, measured by in vitro microperfusion of collecting duct from KO and wild-type mice, was identical with no apparent effect of the absence of Rhbg protein. We conclude that Rhbg is not a critical determinant of NH(4)(+) excretion by the kidney and of NH(4)(+) detoxification by the liver in vivo.