Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4 Pt 2
pubmed:dateCreated
1991-8-23
pubmed:abstractText
The purpose of this investigation was to compare the chronic effects of converting enzyme inhibition with captopril to direct blockade of angiotensin II (AII) with DuP 753 in the rat model of heart failure. Rats with chronic heart failure postinfarction were treated for 2 weeks with either captopril (2 g/L, N = 9) in their drinking water or with DuP 753 (40 mg/kg/day for two weeks by gastric gavage, N = 10), or placebo (N = 9). At this dose, DuP 753 shifted the log dose-pressor response curve to AII parallel to the right by two orders of magnitude in both chronically treated normal and heart failure rats. In rats with heart failure, DuP 753 and captopril reduced left ventricular end-diastolic pressure from 26.7 +/- 1.5 to 14.2 +/- 3.0 (P less than .01) and 15.8 +/- 2.2 mm Hg (P less than .05), respectively, left ventricular end-diastolic volume index from 2.71 +/- 0.10 to 2.03 +/- 0.17 (P less than .05) and 2.18 +/- 0.15 (P less than .05), respectively; venous compliance increased from 2.27 +/- 0.06 to 2.80 +/- 0.18 (P less than .05) and 3.02 +/- 0.21 mL/mm Hg/kg (P less than .01), respectively. There were no significant changes in left ventricular weight/body weight ratio, mean aortic pressure, heart rate, or right atrial pressure. There was a trend, but not significant, for a reduction in total blood volume from 65.8 +/- 1.1 to 59.4 +/- 3.0 and 64.9 +/- 3.9 mL/kg, respectively. Thus, direct blockade of AII with DuP 753 or with converting enzyme inhibition with captopril produces similar hemodynamic changes in rats with heart failure after myocardial infarction.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
0895-7061
pubmed:author
pubmed:issnType
Print
pubmed:volume
4
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
334S-340S
pubmed:dateRevised
2009-2-24
pubmed:meshHeading
pubmed-meshheading:1854461-Administration, Oral, pubmed-meshheading:1854461-Angiotensin II, pubmed-meshheading:1854461-Animals, pubmed-meshheading:1854461-Body Weight, pubmed-meshheading:1854461-Captopril, pubmed-meshheading:1854461-Cardiac Output, Low, pubmed-meshheading:1854461-Compliance, pubmed-meshheading:1854461-Disease Models, Animal, pubmed-meshheading:1854461-Dose-Response Relationship, Drug, pubmed-meshheading:1854461-Heart, pubmed-meshheading:1854461-Hemodynamics, pubmed-meshheading:1854461-Imidazoles, pubmed-meshheading:1854461-Losartan, pubmed-meshheading:1854461-Male, pubmed-meshheading:1854461-Myocardial Infarction, pubmed-meshheading:1854461-Rats, pubmed-meshheading:1854461-Rats, Inbred Strains, pubmed-meshheading:1854461-Tetrazoles, pubmed-meshheading:1854461-Ventricular Function, Left
pubmed:year
1991
pubmed:articleTitle
Hemodynamic effects of direct angiotensin II blockade compared to converting enzyme inhibition in rat model of heart failure.
pubmed:affiliation
Department of Internal Medicine, Tucson Veterans Administration Medical Center, AZ 85723.
pubmed:publicationType
Journal Article, Comparative Study, Research Support, U.S. Gov't, P.H.S., Research Support, U.S. Gov't, Non-P.H.S., Research Support, Non-U.S. Gov't