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WATER METABOLISM IN HYPERTENSIVE RATS

The water intake in hypertensive rats was investigated. Rats made hypertensive by renal ischemia increased their water consumption by 75 per cent over the preoperative level. Polyuria was associated with this polydipsia and the independence of these occurrences from a number of other factors was dem...

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Detalles Bibliográficos
Autores principales: Oster, Kurt A., Martinez, Oscar
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1943
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2135421/
https://www.ncbi.nlm.nih.gov/pubmed/19871343
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author Oster, Kurt A.
Martinez, Oscar
author_facet Oster, Kurt A.
Martinez, Oscar
author_sort Oster, Kurt A.
collection PubMed
description The water intake in hypertensive rats was investigated. Rats made hypertensive by renal ischemia increased their water consumption by 75 per cent over the preoperative level. Polyuria was associated with this polydipsia and the independence of these occurrences from a number of other factors was demonstrated. It was found that the presence of a normal kidney exerted a compensatory influence which may mask either hypertension or polyuria or both. The appearance or exacerbation of the changes upon removal of the normal kidney, on the one hand, and the elimination or mitigation of the symptoms upon removal of the ischemic kidney on the other support the view that the changes observed cannot have been due to passive elimination of the kidney tissue by ischemia, but to active malfunction of the renal, and especially the tubular, mechanism upon withdrawal of oxygen. The view is put forward that polyuria is a primary sequel of ischemia rather than secondary to the intra- and extrarenal effects of hypertension. A number of concomitant observations are in harmony with this hypothesis.
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spelling pubmed-21354212008-04-18 WATER METABOLISM IN HYPERTENSIVE RATS Oster, Kurt A. Martinez, Oscar J Exp Med Article The water intake in hypertensive rats was investigated. Rats made hypertensive by renal ischemia increased their water consumption by 75 per cent over the preoperative level. Polyuria was associated with this polydipsia and the independence of these occurrences from a number of other factors was demonstrated. It was found that the presence of a normal kidney exerted a compensatory influence which may mask either hypertension or polyuria or both. The appearance or exacerbation of the changes upon removal of the normal kidney, on the one hand, and the elimination or mitigation of the symptoms upon removal of the ischemic kidney on the other support the view that the changes observed cannot have been due to passive elimination of the kidney tissue by ischemia, but to active malfunction of the renal, and especially the tubular, mechanism upon withdrawal of oxygen. The view is put forward that polyuria is a primary sequel of ischemia rather than secondary to the intra- and extrarenal effects of hypertension. A number of concomitant observations are in harmony with this hypothesis. The Rockefeller University Press 1943-12-01 /pmc/articles/PMC2135421/ /pubmed/19871343 Text en Copyright © Copyright, 1943, by The Rockefeller Institute for Medical Research New York This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Article
Oster, Kurt A.
Martinez, Oscar
WATER METABOLISM IN HYPERTENSIVE RATS
title WATER METABOLISM IN HYPERTENSIVE RATS
title_full WATER METABOLISM IN HYPERTENSIVE RATS
title_fullStr WATER METABOLISM IN HYPERTENSIVE RATS
title_full_unstemmed WATER METABOLISM IN HYPERTENSIVE RATS
title_short WATER METABOLISM IN HYPERTENSIVE RATS
title_sort water metabolism in hypertensive rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2135421/
https://www.ncbi.nlm.nih.gov/pubmed/19871343
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