Abstract
Uptake of SO(4) (2-) into brush-border membrane vesicles isolated from rat kindey cortex by a Ca(2+)-precipitation method was investigated by using a rapid-filtration technique. Uptake of SO(4) (2-) by the vesicles was osmotically sensitive and represented transport into an intra-vesicular space. Transport of SO(4) (2-) by brush-border membranes was stimulated in the presence of Na(+), compared with the presence of K(+) or other univalent cations. A typical ;overshoot' phenomenon was observed in the presence of an NaCl gradient (100mm-Na(+) outside/zero mm-Na(+) inside). Radioactive-SO(4) (2-) exchange was faster in the presence of Na(+) than in the presence of K(+). Addition of gramicidin-D, an ionophore for univalent cations, decreased the Na(+)-gradient-driven SO(4) (2-) uptake. SO(4) (2-) uptake was only saturable in the presence of Na(+). Counter-transport of Na(+)-dependent SO(4) (2-) transport was shown with MoO(4) (2-) and S(2)O(3) (2-), but not with PO(4) (2-). Changing the electrical potential difference across the vesicle membrane by establishing different diffusion potentials (anion replacement; K(+) gradient+/-valinomycin) was not able to alter Na(+)-dependent SO(4) (2-) uptake. The experiments indicate the presence of an electroneutral Na(+)/SO(4) (2-)-co-transport system in brush-border membrane vesicles isolated from rat kidney cortex.
MeSH Terms
Animals
Biological Transport, Active/drug effects
Cations/pharmacology
Cell Membrane/metabolism
Gramicidin/pharmacology
In Vitro Techniques
Kidney Cortex/metabolism
Male
Mercury/pharmacology
Microvilli/drug effects,metabolism
Nigericin/pharmacology
Rats
Sodium/metabolism
Sulfates/metabolism
Valinomycin/pharmacology
Chemicals
Cations
Sulfates
Gramicidin
Valinomycin
Sodium
Mercury
Nigericin
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Lücke H
Stange G
Murer H
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12 references, click to expand
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