Lactate-sodium cotransport in rat renal brush border membranes

Am J Physiol. 1980 Nov;239(5):F496-506. doi: 10.1152/ajprenal.1980.239.5.F496.

Abstract

Brush border membrane vesicles were obtained from rat kidney cortex through a calcium precipitation method and their transport properties for lactate were studied by a rapid-filtration technique. Transient concentrative uptake of L-lactate was observed in the presence of inwardly directed NaCl gradient, but not in the presence of a KCl, LiCl, RbCl, CsCl, or choline chloride gradient. The sodium-dependent L-lactate uptake was saturable and was inhibited by D-lactate. The activation curve with sodium was hyperbolic. Maneuvers that render the inside of the vesicle more negative stimulated sodium-dependent L-lactate uptake, suggesting an electrogenic transfer of L-lactate and sodium. An L-lactate gradient also accelerates the sodium movement across the brush border membrane. Studies on the pH dependency of L-lactate transport and on the effect of L-lactate on proton movements across the brush border membrane indicate that there is little contribution of nonionic diffusion and/or of lactate-H+ cotransport to the transfer of L-lactate across the renal brush border membrane. In summary, sodium-lactate cotransport is the major mechanism for L-lactate transfer across the renal brush border membrane.

MeSH terms

  • Animals
  • Biological Transport, Active / drug effects
  • Cell-Free System
  • Glucose / metabolism
  • Gramicidin / pharmacology
  • Hydrogen-Ion Concentration
  • Kidney Cortex / metabolism*
  • Lactates / metabolism*
  • Male
  • Membrane Potentials
  • Microvilli / metabolism
  • Rats
  • Sodium / metabolism*

Substances

  • Lactates
  • Gramicidin
  • Sodium
  • Glucose