Document Detail


Lisinopril and ramiprilat protection of the vascular endothelium against free radical-induced functional injury.
MedLine Citation:
PMID:  1320684     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
We reported earlier that the vasodilator response to acetylcholine (ACh) in lungs exposed to indomethacin and preconstricted with an analog of thromboxane (U46619) is converted to vasoconstriction by brief electrolysis of inflowing perfusion medium and suggested that this effect reflected endothelial injury. The purpose of our present study was 2-fold. First, because captopril, a sulfhydryl-containing inhibitor of angiotensin-converting enzyme inhibitor, prevented this effect (we assumed by scavenging electrolysis generated free radicals of oxygen), we determined whether two angiotensin-converting enzyme inhibitors lacking this moiety, namely lisinopril and ramiprilat, provided similar protection. Second, we studied whether electrolysis, like other forms of experimental lung injury, impaired uptake of serotonin (5-HT) by the endothelium. Our study confirmed that within 5 min of electrolytic injury, the ACh response is converted to vasoconstriction. This effect was completely prevented by lisinopril (18 microM) or ramiprilat (30 microM), neither of which affected ACh vasodilatation in control lungs. Lower concentrations of either drug exerted lesser degrees of protection. Five or 20 min after electrolysis, single-pass uptake of [14C]5-HT was significantly (P less than .01; N = 11) lower than control (82.4 +/- 3.4% vs. 71 +/- 3.2 and 46.5 +/- 6%, respectively). In contrast, 5-HT uptake was unaltered by electrolysis in the presence of 18 microM lisinopril. We conclude that loss of ACh vasodilation is an early reflection of lung endothelial injury that is accompanied by reduced [14C]5-HT uptake. Also, the protective property of nonsulfhydryl-containing angiotensin-converting enzyme inhibitors may be related to unexpected antioxidant actions.
Authors:
C N Gillis; X Chen; M M Merker
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Publication Detail:
Type:  Journal Article; Research Support, U.S. Gov't, P.H.S.    
Journal Detail:
Title:  The Journal of pharmacology and experimental therapeutics     Volume:  262     ISSN:  0022-3565     ISO Abbreviation:  J. Pharmacol. Exp. Ther.     Publication Date:  1992 Jul 
Date Detail:
Created Date:  1992-08-11     Completed Date:  1992-08-11     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:  212-6     Citation Subset:  IM    
Affiliation:
Department of Anesthesiology, Yale University School of Medicine, New Haven, Connecticut.
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MeSH Terms
Descriptor/Qualifier:
15-Hydroxy-11 alpha,9 alpha-(epoxymethano)prosta-5,13-dienoic Acid
Angiotensin-Converting Enzyme Inhibitors / pharmacology*
Animals
Enalapril / analogs & derivatives*,  pharmacology
Endothelium, Vascular / drug effects*
Free Radicals / antagonists & inhibitors
Lisinopril
Lung / drug effects,  metabolism
Male
Prostaglandin Endoperoxides, Synthetic / pharmacology
Pyrroles / pharmacology*
Rabbits
Ramipril* / analogs & derivatives*
Serotonin / metabolism
Vasoconstrictor Agents / pharmacology
Grant Support
ID/Acronym/Agency:
HL13315/HL/NHLBI NIH HHS; HL40863/HL/NHLBI NIH HHS
Chemical
Reg. No./Substance:
0/Angiotensin-Converting Enzyme Inhibitors; 0/Free Radicals; 0/Prostaglandin Endoperoxides, Synthetic; 0/Pyrroles; 0/Vasoconstrictor Agents; 50-67-9/Serotonin; 75847-73-3/Enalapril; 76898-47-0/15-Hydroxy-11 alpha,9 alpha-(epoxymethano)prosta-5,13-dienoic Acid; 83915-83-7/Lisinopril; 87269-97-4/ramiprilat; 87333-19-5/Ramipril

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


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