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      Sodium-Dependent Ascorbic and Dehydroascorbic Acid Uptake by SV-40-Transformed Retinal Pigment Epithelial Cells

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          Abstract

          The present data confirmed previous studies with other cell types that ascorbic acid and dehydroascorbic acid are transported through different transporters into SV-40-transformed retinal pigment epithelial cells. These experiments were performed on cells grown on 96-well culture plates. Ascorbic acid was taken up into the cell by a high-affinity transporter with K<sub>m</sub> = 0.041 mmol/l and a low Vmax of 2.74 pmol/min/well. Dehydroascorbic acid was taken up by a low-affinity transporter with K<sub>m</sub> = 5.67 mmol/l; however, the V<sub>max</sub> was 325.5 pmol/min/well. The uptake of both ascorbic acid and dehydroascorbic acid was dependent on the sodium concentration. The uptake of ascorbic acid does not involve oxidation-reaction steps because the uptake of [<sup>14</sup>C]-ascorbate was unaffected by the presence of an excess amount of unlabelled dehydroascorbic acid.

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          Author and article information

          Journal
          ORE
          Ophthalmic Res
          10.1159/issn.0030-3747
          Ophthalmic Research
          S. Karger AG
          0030-3747
          1423-0259
          1993
          1993
          11 December 2009
          : 25
          : 2
          : 100-107
          Affiliations
          aDepartment of Ophthalmology, University of Texas Health Science Center at San Antonio; bBiorhythm Research Laboratory, Division of Mathematics, Computer Science, and Statistics, University of Texas at San Antonio, Tex., USA
          Article
          267272 Ophthalmic Res 1993;25:100–107
          10.1159/000267272
          8391673
          2fb0a979-06ce-4d14-8529-93be0cfd0247
          © 1993 S. Karger AG, Basel

          Copyright: All rights reserved. No part of this publication may be translated into other languages, reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying, recording, microcopying, or by any information storage and retrieval system, without permission in writing from the publisher. Drug Dosage: The authors and the publisher have exerted every effort to ensure that drug selection and dosage set forth in this text are in accord with current recommendations and practice at the time of publication. However, in view of ongoing research, changes in government regulations, and the constant flow of information relating to drug therapy and drug reactions, the reader is urged to check the package insert for each drug for any changes in indications and dosage and for added warnings and precautions. This is particularly important when the recommended agent is a new and/or infrequently employed drug. Disclaimer: The statements, opinions and data contained in this publication are solely those of the individual authors and contributors and not of the publishers and the editor(s). The appearance of advertisements or/and product references in the publication is not a warranty, endorsement, or approval of the products or services advertised or of their effectiveness, quality or safety. The publisher and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements.

          History
          : 15 April 1992
          : 07 October 1992
          Page count
          Pages: 8
          Categories
          Original Paper

          Vision sciences,Ophthalmology & Optometry,Pathology
          Oxidative reduction,Dehydroascorbate,Sodium,Ascorbate,Active transport,Retinal pigment epithelium

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