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PRESSOR SUBSTANCES IN ARTERIAL HYPERTENSION : V. CHEMICAL AND PHARMACOLOGICAL CHARACTERISTICS OF PHERENTASIN

Some pharmacological and chemical qualities of pherentasin, a vasoconstrictor substance procured from human hypertensive blood, were studied by a new assay method using the spirally cut rabbit aorta. Of a number of drugs tested, six metal-binding agents including hydralazine inactivated the active p...

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Detalles Bibliográficos
Autores principales: Schroeder, Henry A., Perry, H. Mitchell, Dennis, Evie G., Mahoney, Laura E.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1955
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2136506/
https://www.ncbi.nlm.nih.gov/pubmed/13252186
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author Schroeder, Henry A.
Perry, H. Mitchell
Dennis, Evie G.
Mahoney, Laura E.
author_facet Schroeder, Henry A.
Perry, H. Mitchell
Dennis, Evie G.
Mahoney, Laura E.
author_sort Schroeder, Henry A.
collection PubMed
description Some pharmacological and chemical qualities of pherentasin, a vasoconstrictor substance procured from human hypertensive blood, were studied by a new assay method using the spirally cut rabbit aorta. Of a number of drugs tested, six metal-binding agents including hydralazine inactivated the active principle. The material was stable in acid but not in alkali. It was destroyed by drying. Chemical analysis and inactivation procedures suggested the presence of primary amine and considerable sulfur; a peptide linkage was suspected because of inactivation by manganous ion and papain. The material was remarkably resistant to most pharmacological agents and appeared to act directly on smooth muscle.
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spelling pubmed-21365062008-04-17 PRESSOR SUBSTANCES IN ARTERIAL HYPERTENSION : V. CHEMICAL AND PHARMACOLOGICAL CHARACTERISTICS OF PHERENTASIN Schroeder, Henry A. Perry, H. Mitchell Dennis, Evie G. Mahoney, Laura E. J Exp Med Article Some pharmacological and chemical qualities of pherentasin, a vasoconstrictor substance procured from human hypertensive blood, were studied by a new assay method using the spirally cut rabbit aorta. Of a number of drugs tested, six metal-binding agents including hydralazine inactivated the active principle. The material was stable in acid but not in alkali. It was destroyed by drying. Chemical analysis and inactivation procedures suggested the presence of primary amine and considerable sulfur; a peptide linkage was suspected because of inactivation by manganous ion and papain. The material was remarkably resistant to most pharmacological agents and appeared to act directly on smooth muscle. The Rockefeller University Press 1955-09-01 /pmc/articles/PMC2136506/ /pubmed/13252186 Text en Copyright © Copyright, 1955, by The Rockefeller Institute for Medical Research New York This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Article
Schroeder, Henry A.
Perry, H. Mitchell
Dennis, Evie G.
Mahoney, Laura E.
PRESSOR SUBSTANCES IN ARTERIAL HYPERTENSION : V. CHEMICAL AND PHARMACOLOGICAL CHARACTERISTICS OF PHERENTASIN
title PRESSOR SUBSTANCES IN ARTERIAL HYPERTENSION : V. CHEMICAL AND PHARMACOLOGICAL CHARACTERISTICS OF PHERENTASIN
title_full PRESSOR SUBSTANCES IN ARTERIAL HYPERTENSION : V. CHEMICAL AND PHARMACOLOGICAL CHARACTERISTICS OF PHERENTASIN
title_fullStr PRESSOR SUBSTANCES IN ARTERIAL HYPERTENSION : V. CHEMICAL AND PHARMACOLOGICAL CHARACTERISTICS OF PHERENTASIN
title_full_unstemmed PRESSOR SUBSTANCES IN ARTERIAL HYPERTENSION : V. CHEMICAL AND PHARMACOLOGICAL CHARACTERISTICS OF PHERENTASIN
title_short PRESSOR SUBSTANCES IN ARTERIAL HYPERTENSION : V. CHEMICAL AND PHARMACOLOGICAL CHARACTERISTICS OF PHERENTASIN
title_sort pressor substances in arterial hypertension : v. chemical and pharmacological characteristics of pherentasin
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2136506/
https://www.ncbi.nlm.nih.gov/pubmed/13252186
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