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- W2023574609 abstract "Tolrestat, and aldose-reductase inhibitor, was shown to be a rapid and potent inhibitor of chloride exchange on the band 3 protein of human erythrocytes. Tolrestat binds to a site distinct from the chloride transport site and binds to one half of the transporters at 5 × 10−7 mol/L in the absence of chloride and at 3.6 × 10−5 mol/L in physiologic chloride concentrations. Although these concentrations are 20- to 1,000-fold greater than the IC50 for aldose-reductase inhibition by tolrestat, they are achieved during routine pharmacologic therapy in humans. Consequently, exchange rates may be reduced, and there may be decreased CO2 clearance from coronary and respiratory center capillary beds and inappropriate hyperpnea. There also may be transitory intracellular alkalinization in cells with a exchanger in their plasma membrane." @default.
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- W2023574609 date "1989-08-01" @default.
- W2023574609 modified "2023-09-27" @default.
- W2023574609 title "Inhibition of erythrocyte anion exchange by tolrestat, an inhibitor of aldose reductase" @default.
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- W2023574609 doi "https://doi.org/10.1016/0026-0495(89)90070-x" @default.
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