avian kidney
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Author(s):  
A. Milton ◽  
B. Odlind ◽  
L. Wibell ◽  
L. Dencker
Keyword(s):  

2009 ◽  
Vol 36 (2) ◽  
pp. 195-198 ◽  
Author(s):  
A. Nabipour ◽  
E. Alishahi ◽  
M. Asadian
Keyword(s):  

2006 ◽  
Vol 20 (5) ◽  
Author(s):  
Karen L. Sweazea ◽  
Giovanni Casotti ◽  
Eldon J. Braun
Keyword(s):  

2005 ◽  
Vol 66 (6) ◽  
pp. 275-288 ◽  
Author(s):  
Andrew N. Makanya ◽  
Daniela Stauffer ◽  
Domenico Ribatti ◽  
Peter H. Burri ◽  
Valentin Djonov

2002 ◽  
Vol 283 (4) ◽  
pp. C1155-C1162 ◽  
Author(s):  
Steven M. Grassl

Membrane transport pathways mediating transcellular secretion of urate across the proximal tubule were investigated in brush-border membrane vesicles (BBMV) isolated from avian kidney. An inside-positive K diffusion potential induced a conductive uptake of urate to levels exceeding equilibrium. Protonophore-induced dissipation of membrane potential significantly reduced voltage-driven urate uptake. Conductive uptake of urate was inhibitor sensitive, substrate specific, and a saturable function of urate concentration. Urate uptake was trans-stimulated by urate and cis-inhibited by p-aminohippurate (PAH). Conductive uptake of PAH was cis-inhibited by urate. Urate uptake was unaffected by an outward α-ketoglutarate gradient. In the absence of a membrane potential, urate uptake was similar in the presence and absence of an imposed inside-alkaline pH gradient or an outward Cl gradient. These observations suggest a uniporter-mediated facilitated diffusion of urate as a pathway for passive efflux across the brush border membrane of urate-secreting proximal tubule cells.


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