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      Effects of Val 5-Angiotensin II-Amide and of Hydrochlorothiazide on the Kidneys of Renal Hypertensive Rats

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      Publication date (Electronic):
      Journal: Nephron
      Publisher: S. Karger AG

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          Abstract

          Angiotensin II-amide administered intravenously at 0.2 µg/kg·min together with isotonic saline to rats with either DCA-induced or renal hypertension had the same diuretic and natriuretic effects as in normal rats. In renal hypertension (induced by a clip on one renal artery leaving the other kidney untouched) the normal overall diuretic response appeared to be due to the clamped kidney only. In the unclamped kidney of renal hypertensive rats the tubular diuretic and natriuretic response to angiotensin was abolished. Hydrochlorothiazide (5 mg/kg i.v., followed by 1 mg/kg •min) also failed to elicit its normal natriuretic response in the unclamped kidney. This failure, apparently, was the consequence of a greater depression of GFR (C<sub>In</sub>) in the unclamped kidney.

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          Author and article information

          Journal
          Journal ID (publisher-id): NEF
          Journal ID (nlm-ta): Nephron
          Journal ID (doi): 10.1159/issn.1660-8151
          Title: Nephron
          Publisher: S. Karger AG
          ISSN (Print): 1660-8151
          ISSN (Electronic): 2235-3186
          Publication date Subscription-year: 1965
          Publication date (Print): 1965
          Publication date (Electronic): 25 November 2008
          Volume: 2
          Issue: 2
          Pages: 95-106
          Affiliations
          Department of Pharmacology, University of Lausanne, and Research Laboratories, Pharmaceutical Department, CIBA Limited, Basle
          Article
          Publisher ID: 179379 Other ID: Nephron 1965;2:95–106
          DOI: 10.1159/000179379
          PubMed ID: 4284015
          SO-VID: 8640506a-79c2-48ad-9758-df67f2bad880
          Copyright © © 1965 S. Karger AG, Basel
          License:

          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
          Page count
          Pages: 12
          Categories
          Subject: Paper

          ScienceOpen disciplines: Cardiovascular Medicine,Nephrology
          Data availability:
          ScienceOpen disciplines: Cardiovascular Medicine, Nephrology

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