Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
7
pubmed:dateCreated
1995-8-11
pubmed:abstractText
The iv administration of L-arginine, a precursor of endothelium-derived relaxing factor/nitric oxide, is known to decrease blood pressure in humans by its direct vasodilatory effects. The purpose of the present study was to determine whether L-arginine infusion modifies the renin-angiotensin (Ang)-aldosterone system as well as blood pressure and renal hemodynamics. L-Arginine and saline vehicle were iv administered to 10 healthy male subjects in random order on different days. L-Arginine infusion (500 mg/kg over 30 min) decreased mean blood pressure (from 81.2 +/- 2.7 to 74.0 +/- 2.5 mm Hg; P < 0.001) and renal vascular resistance (from 0.085 +/- 0.007 to 0.074 +/- 0.006 mm Hg/mL.min; P < 0.01) and increased heart rate (from 60.3 +/- 2.7 to 69.7 +/- 2.1 beats/min; P < 0.001) and renal plasma flow (from 616.6 +/- 37.8 to 701.0 +/- 49.2 mL/min; P < 0.05). L-Arginine reduced serum Ang-converting enzyme activity (from 10.4 +/- 0.6 to 8.9 +/- 0.5 nmol/mL.min; P < 0.05) and plasma Ang-II (from 19.3 +/- 3.3 to 12.7 +/- 2.8 pg/mL; P < 0.001), but had no effect on PRA or the glomerular filtration rate. The saline vehicle did not alter any of these parameters. The iv administration of L-arginine (endothelium-derived relaxing factor/nitric oxide) may reduce the plasma Ang-II concentration by inhibiting Ang-converting enzyme. The mechanism by which L-arginine infusion decreases blood pressure can be at least in part explained by inhibition of the renin-Ang system.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
0021-972X
pubmed:author
pubmed:issnType
Print
pubmed:volume
80
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2198-202
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:7608279-Adult, pubmed-meshheading:7608279-Aldosterone, pubmed-meshheading:7608279-Angiotensin II, pubmed-meshheading:7608279-Angiotensin-Converting Enzyme Inhibitors, pubmed-meshheading:7608279-Arginine, pubmed-meshheading:7608279-Blood Pressure, pubmed-meshheading:7608279-Cyclic GMP, pubmed-meshheading:7608279-Glomerular Filtration Rate, pubmed-meshheading:7608279-Heart Rate, pubmed-meshheading:7608279-Humans, pubmed-meshheading:7608279-Infusions, Intravenous, pubmed-meshheading:7608279-Insulin, pubmed-meshheading:7608279-Male, pubmed-meshheading:7608279-Peptidyl-Dipeptidase A, pubmed-meshheading:7608279-Reference Values, pubmed-meshheading:7608279-Renal Circulation, pubmed-meshheading:7608279-Renin, pubmed-meshheading:7608279-Time Factors, pubmed-meshheading:7608279-Vascular Resistance
pubmed:year
1995
pubmed:articleTitle
Intravenous administration of L-arginine inhibits angiotensin-converting enzyme in humans.
pubmed:affiliation
First Department of Internal Medicine, Hiroshima University School of Medicine, Japan.
pubmed:publicationType
Journal Article, Clinical Trial, Comparative Study, Randomized Controlled Trial, Research Support, Non-U.S. Gov't