Voltage-driven p-aminohippurate, chloride, and urate transport in porcine renal brush-border membrane vesicles

Pflugers Arch. 2000 Nov;441(1):125-32. doi: 10.1007/s004240000378.


p-Aminohippurate (PAH) and urate are secreted into the proximal tubule lumen across the brush-border membrane. Here we used brush-border membrane vesicles from pig kidney to study PAH and urate transport. Efflux and influx of [3H]PAH were influenced by K+-diffusion potentials indicating electrogenic PAH transport. An outside>inside PAH concentration difference accelerated voltage-sensitive, Na+-coupled D-glucose uptake as efficiently as did an outside>inside Cl- concentration difference, suggesting comparable conductances for PAH and Cl- in brush-border membrane vesicles. Up to 1 mM of the uricosurics indacrinone, tienilic acid, losartan and probenecid, as well as of the stilbenes, DIDS and SITS, and of the loop diuretics furosemide and bumetanide inhibited voltage-driven PAH uptake, but not, or only slightly, voltage-driven Cl- uptake. Voltage-driven [14C]urate uptake, however, was inhibited by 0.1 mM DIDS, 0.2 mM losartan and 0.5 mM probenecid to a similar extent as [3H]PAH uptake. One millimolar pyrazinoic acid, oxonate, xanthine and adenosine inhibited neither [3H]PAH nor [14C]urate uptake. These results suggest that PAH and urate share an anion conductance which is distinct from the Cl- conductance and is probably not the same as a recently identified urate channel (Leal-Pinto E et a]. J Biol Chem 272:617-625, 1997).

MeSH terms

  • 4,4'-Diisothiocyanostilbene-2,2'-Disulfonic Acid / pharmacology
  • Animals
  • Biological Transport / drug effects
  • Bumetanide / pharmacology
  • Cell Membrane Permeability
  • Chlorides / metabolism*
  • Diffusion
  • Diuretics / pharmacology
  • Furosemide / pharmacology
  • Glucose / metabolism
  • Ionophores / pharmacology
  • Kidney / ultrastructure*
  • Kidney Tubules, Proximal / metabolism
  • Membrane Potentials*
  • Microvilli / metabolism*
  • Potassium / metabolism
  • Potassium / pharmacology
  • Sodium / pharmacology
  • Swine
  • Tritium
  • Uric Acid / metabolism*
  • Valinomycin / pharmacology
  • p-Aminohippuric Acid / metabolism


  • Chlorides
  • Diuretics
  • Ionophores
  • Bumetanide
  • Tritium
  • Valinomycin
  • Uric Acid
  • Furosemide
  • Sodium
  • Glucose
  • 4,4'-Diisothiocyanostilbene-2,2'-Disulfonic Acid
  • Potassium
  • p-Aminohippuric Acid