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pubmed-article:8619846pubmed:abstractTextA potent inhibitor of the Na-K-Cl cotransport system was purified from urines of salt-loaded rats. Mass spectroscopy revealed a molecular mass of 242 Da. Nuclear magnetic resonance showed a spectrum identical to that of 3,4-dihydro-3-(4-hydroxyphenyl)-2H-1-benzopyran-7-ol (an "estrogen-like" isoflavonoid: equol). This compound inhibited cotransport fluxes at similar concentrations (IC50=16-24 microM) as furosemide (IC50 approximately 10 microM). Cotransport inhibitory activity of urines from rats drinking tap water was fully explained by urinary equol concentrations (approximately 27 microM, measured by high-performance liquid chromatography). Slat-loading increased urinary equol excretion, but not sufficiently high to fully explain the very important increase in cotransport inhibitory potency. We conclude that: (i) under basal conditions urinary equol can regulate Na-K-Cl cotransport activity in the kidney and (ii) salt-loading should evoke the appearance of other cotransport inhibitors.lld:pubmed
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pubmed-article:8619846pubmed:dateRevised2011-11-17lld:pubmed
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pubmed-article:8619846pubmed:year1996lld:pubmed
pubmed-article:8619846pubmed:articleTitlePurification and chemical characterization of a potent inhibitor of the Na-K-Cl cotransport system in rat urine.lld:pubmed
pubmed-article:8619846pubmed:affiliationPhysiology and Pharmacology, School of Medicine, University of Zaragoza, Spain.lld:pubmed
pubmed-article:8619846pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:8619846pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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