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Concise Publication Free access | 10.1172/JCI107393

A Saturable, Vasopressin-Sensitive Carrier for Urea and Acetamide in the Toad Bladder Epithelial Cell

Sherman Levine, Nicholas Franki, and Richard M. Hays

1Department of Medicine, Division of Nephrology, Albert Einstein College of Medicine, Bronx, New York 10461

Find articles by Levine, S. in: JCI | PubMed | Google Scholar

1Department of Medicine, Division of Nephrology, Albert Einstein College of Medicine, Bronx, New York 10461

Find articles by Franki, N. in: JCI | PubMed | Google Scholar

1Department of Medicine, Division of Nephrology, Albert Einstein College of Medicine, Bronx, New York 10461

Find articles by Hays, R. in: JCI | PubMed | Google Scholar

Published August 1, 1973 - More info

Published in Volume 52, Issue 8 on August 1, 1973
J Clin Invest. 1973;52(8):2083–2086. https://doi.org/10.1172/JCI107393.
© 1973 The American Society for Clinical Investigation
Published August 1, 1973 - Version history
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Abstract

The permeability of the toad bladder to a series of isotopically labeled nonelectrolytes was determined in the presence of 150 mM unlabeled acetamide. Under these conditions, overall bladder function was unimpaired, as shown by a normal response to vasopressin of short-circuit current and permeability coefficient of [3H]water,[14C]ethanol, and [14C]propionamide. The permeability of the bladder to isotopic acetamide and urea, however, was significantly depressed by unlabeled acetamide, in both the absence and presence of vasopressin. These experiments indicate a competition between unlabeled and isotopic species for binding sites, and show the existence of a saturable, vasopressin-sensitive carrier for urea and acetamide in the epithelial cell membrane.

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