Document Detail


Vascular reactivity to angiotensin II is selectively enhanced in the kidneys of spontaneously hypertensive rats.
MedLine Citation:
PMID:  8169855     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The two aims of the present study were to: 1) explore the hypothesis that the kidneys of spontaneously hypertensive rats (SHR) are more responsive to angiotensin II (Ang II) than are the kidneys of normotensive Wistar Kyoto rats (WKY) and 2) determine whether other vascular beds of SHR exhibit enhanced responsiveness to Ang II, relative to WKY. SHR and WKY received captopril from 4 weeks of age until the time of the experiment to prevent vascular alterations secondary to hypertension. Blood pressure, heart rate, cardiac output and blood flow through the superior mesenteric artery, left renal artery, lower abdominal aorta and right carotid artery were monitored in anesthetized SHR and WKY during acute i.v. administration of Ang II at doses of 0, 3, 10, 30, 100 and 300 ng kg-1 min-1. The heart rate and cardiac output were not significantly affected but the blood pressure was increased to a similar extent in both strains during the Ang II infusion. Hindquarter (aortic) resistance was unaffected by Ang II in both strains. Carotid resistance was slightly increased by the peptide to a similar magnitude in SHR and WKY. The renal and mesenteric vasculature of both strains were highly sensitive to Ang II, with significant dose-related increases in resistance during the infusion. The magnitude of the mesenteric response was not different between SHR and WKY. However, the renal vascular response to Ang II was significantly greater in SHR than in WKY. In conclusion, the enhanced responsiveness to i.v. Ang II occurred selectively in the kidney of SHR and not in the other vessels examined.
Authors:
C K Kost; W A Herzer; P Li; E K Jackson
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Publication Detail:
Type:  Comparative Study; Journal Article; Research Support, U.S. Gov't, P.H.S.    
Journal Detail:
Title:  The Journal of pharmacology and experimental therapeutics     Volume:  269     ISSN:  0022-3565     ISO Abbreviation:  J. Pharmacol. Exp. Ther.     Publication Date:  1994 Apr 
Date Detail:
Created Date:  1994-06-02     Completed Date:  1994-06-02     Revised Date:  2007-11-14    
Medline Journal Info:
Nlm Unique ID:  0376362     Medline TA:  J Pharmacol Exp Ther     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  82-8     Citation Subset:  IM    
Affiliation:
Center for Clinical Pharmacology, University of Pittsburgh Medical Center, Pennsylvania.
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MeSH Terms
Descriptor/Qualifier:
Angiotensin II / pharmacology*
Animals
Arteries / drug effects,  physiology
Blood Pressure / drug effects
Captopril / therapeutic use
Cardiac Output / drug effects
Heart Rate / drug effects
Hypertension / complications,  prevention & control
Infusions, Intravenous
Kidney / blood supply*,  drug effects*
Rats
Rats, Inbred SHR
Rats, Inbred WKY
Species Specificity
Vascular Diseases / etiology,  prevention & control
Vascular Resistance / drug effects
Grant Support
ID/Acronym/Agency:
HL14192/HL/NHLBI NIH HHS; HL35909/HL/NHLBI NIH HHS
Chemical
Reg. No./Substance:
11128-99-7/Angiotensin II; 62571-86-2/Captopril

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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