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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3 Pt 2
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pubmed:dateCreated |
1990-4-23
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pubmed:abstractText |
Rabbit renal brush-border membrane vesicles (BBMV) were used to study the transport of the cationic neurotoxin, 1-methyl-4-phenylpyridinium (MPP+). An outwardly directed H(+)-gradient stimulated MPP+ uptake and led to the development of an active accumulation of MPP+ within the vesicles. H(+)-gradient driven MPP+ transport was saturable, with a maximal transport rate of 3 nmol.mg-1.min-1 and an apparent Michaelis constant (Kt) of 8 microM. MPP+ and tetraethylammonium (TEA) behaved as competitive inhibitors of one another's transport in renal BBMV, suggesting the presence of a common transport pathway for these organic cations. At an ambient pH of 7.5, preloading BBMV with MPP+ failed to stimulate TEA uptake, although trans TEA did stimulate MPP+ uptake. Increasing ambient pH to 8.5 (i.e., reducing competition between H+ and these organic cations for a common transport pathway) led to a clear reciprocal trans stimulation of TEA and MPP+ fluxes. With an equilibrium-shift protocol, a trans concentration of MPP+ energized uphill transport of TEA. We conclude that MPP+ and TEA share a common organic cation-H+ exchange pathway in the renal brush border, although turnover of an MPP(+)-loaded exchanger is slow compared with that for a TEA or H(+)-loaded exchanger.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/1-Methyl-4-phenylpyridinium,
http://linkedlifedata.com/resource/pubmed/chemical/Cations,
http://linkedlifedata.com/resource/pubmed/chemical/Hydrogen,
http://linkedlifedata.com/resource/pubmed/chemical/Ions,
http://linkedlifedata.com/resource/pubmed/chemical/Tetraethylammonium,
http://linkedlifedata.com/resource/pubmed/chemical/Tetraethylammonium Compounds
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0002-9513
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
258
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
F597-605
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:2316668-1-Methyl-4-phenylpyridinium,
pubmed-meshheading:2316668-Animals,
pubmed-meshheading:2316668-Biological Transport,
pubmed-meshheading:2316668-Cations,
pubmed-meshheading:2316668-Hydrogen,
pubmed-meshheading:2316668-Hydrogen-Ion Concentration,
pubmed-meshheading:2316668-Ions,
pubmed-meshheading:2316668-Kidney,
pubmed-meshheading:2316668-Kinetics,
pubmed-meshheading:2316668-Microvilli,
pubmed-meshheading:2316668-Osmolar Concentration,
pubmed-meshheading:2316668-Rabbits,
pubmed-meshheading:2316668-Tetraethylammonium,
pubmed-meshheading:2316668-Tetraethylammonium Compounds,
pubmed-meshheading:2316668-Time Factors
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pubmed:year |
1990
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pubmed:articleTitle |
MPP+ is transported by the TEA(+)-H+ exchanger of renal brush-border membrane vesicles.
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pubmed:affiliation |
Department of Pharmacology and Toxicology, College of Pharmacy, University of Arizona, Tucson 85724.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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