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American journal of physiology. Renal physiology, 1991-09, Vol.261 (3), p.386-F392
1991

Details

Autor(en) / Beteiligte
Titel
Basolateral tetraethylammonium transport in intact tubules: specificity and trans-stimulation
Ist Teil von
  • American journal of physiology. Renal physiology, 1991-09, Vol.261 (3), p.386-F392
Ort / Verlag
United States
Erscheinungsjahr
1991
Link zum Volltext
Quelle
MEDLINE
Beschreibungen/Notizen
  • W. H. Dantzler, S. H. Wright, V. Chatsudthipong and O. H. Brokl Department of Physiology, College of Medicine, University of Arizona, Tucson 85724. To examine the specificity of proximal renal basolateral organic cation transport, the effects of unlabeled organic cation substrates in the bathing medium on the rate of uptake [14C]tetraethylammonium ([14C]TEA) by intact nonperfused proximal tubules and isolated basolateral membrane vesicles (BLMV) from rabbit kidneys were explored. The pattern of inhibition of transport by a battery of unlabeled organic cations was similar in intact tubules and BLMV. To determine if trans-stimulation could be demonstrated across the basolateral membrane of intact tubules, the effects of preloading tubules with unlabeled substrates on the rate of uptake of [14C]TEA and the effects of unlabeled substrates in the bathing medium on the rate of efflux of [14C]TEA from tubules preloaded with this labeled substrate were examined. Trans-stimulation was clearly demonstrated for the first time in intact tubules. However, of the compounds that significantly inhibited [14C]TEA uptake (TEA, amiloride, tetrapropylammonium, mepiperphenidol, isopropyl pyridinium, and choline), only TEA itself and choline produced a trans-stimulation of [14C]TEA uptake. Moreover, choline appeared to be at least as effective as TEA itself as a counter ion for TEA transport. Such trans-stimulation could play a physiological role in the net reabsorption of choline and the net secretion of most other organic cations.
Sprache
Englisch
Identifikatoren
ISSN: 0363-6127, 0002-9513, 1931-857X
eISSN: 2161-1157, 2163-5773, 1522-1466
DOI: 10.1152/ajprenal.1991.261.3.F386
Titel-ID: cdi_pubmed_primary_1887903

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