Some aspects of proximal tubular sodium chloride reabsorption in Necturus kidney

Détails

ID Serval
serval:BIB_EC16245B04CA
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Some aspects of proximal tubular sodium chloride reabsorption in Necturus kidney
Périodique
Kidney International
Auteur⸱e⸱s
Whittembury  G., Diezi  F., Diezi  J., Spring  K., Giebisch  G.
ISSN
0085-2538
Statut éditorial
Publié
Date de publication
05/1975
Peer-reviewed
Oui
Volume
7
Numéro
5
Pages
293-30
Notes
Journal Article --- Old month value: May
Résumé
Some aspects of proximal tubular sodium chloride reabsorption in Necturus kidney. Renal tubular reabsorption of fluid and sodium was measured by clearance methods in the doubly perfused Necturus kidney in which the bicarbonate concentration was varied between 0 and 60 mEq/liter. The effects of Damox (2.2 times 10-3M), ocubain (10-5M) and ethacrynic acid (10-4M) and of acidosis were also investigated. In addition to clearance experiments, stationary microperfusion experiments were carried out on promimal tubules to measure volume flow and steady-state sodium and chloride concentration differences across the tubular epithelium. In some experiments, the transepithelial electrical potential difference was also measured using an axial electrode system. The following results were obtained: 1) Bicarbonate is not essential to the operation of renal tubular fluid and sodium transport. 2) Total renal and proximal tubular fluid and sodium transport are partially inhibited by Diamox, ouabian and ethacrynic acid. 3) The proximal tubule maintains a significant transepithelial sodium and chloride concentration difference and a significant electrical potential difference (lumen-negative) in the presence of a poorly permeant nonelectrolyte. The direction and magnitude of the electrical polarization fully accounts for the observed chloride concentration difference. The data support the thesis that sodium chloride transport accross the proximal tubular epithelium takes place by active sodium transport and electically coupled passive chloride reabsorption. Important species differences with respect to mammalian transport mechanisms are discussed.
Mots-clé
Action Potentials Animals Bicarbonates/pharmacology Biological Transport, Active Chlorides/metabolism Ethacrynic Acid/pharmacology Hydrogen-Ion Concentration Kidney Tubules, Proximal/drug effects/*metabolism Metabolic Clearance Rate/drug effects Ouabain/pharmacology Sodium/metabolism Sodium Chloride/*metabolism Urodela
Pubmed
Web of science
Open Access
Oui
Création de la notice
21/01/2008 12:54
Dernière modification de la notice
20/08/2019 17:14
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